DRAVP_ID	Sequence	Sequence_Length	Name	Source	Target_Organism	Patent_Type	Patent_No	Publication_Date	Family_Info	Patent_Title	Comment	Abstract
DRAVP01566	IPLRGAFINGRWDSQCHRFSNGAIACA	27	Sequence 1 from Patent US 20190367567(Urumin)	Synthetic construct	"H1N1,H1N2"	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide exhibits no toxicity to human red blood cells.IC50=2.5-5 ¦ÌM tested by graded concentrations of Urumin (0.6-320 ¦ÌM) against PR8 virus by plaque assay.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01567	SIFSLFKMGAKALGKTLLKQAGKAGAEYAACKATNQC	37	Sequence 2 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01568	SFVTKLKDVAIGVAKGAGLGILKTLTCKLDNSCA	34	Sequence 3 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01569	SFITKLKDVAIGVAKGAGLGILKTLTCKLDNSCA	34	Sequence 4 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01570	APLRGAFINGRWDSQCHRFSNGAIACA	27	Sequence 5 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01571	IALRGAFINGRWDSQCHRFSNGAIACA	27	Sequence 6 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01572	IPARGAFINGRWDSQCHRFSNGAIACA	27	Sequence 7 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01573	IPLAGAFINGRWDSQCHRFSNGAIACA	27	Sequence 8 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01574	IPLRAAFINGRWDSQCHRFSNGAIACA	27	Sequence 9 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01575	IPLRGAAINGRWDSQCHRFSNGAIACA	27	Sequence 10 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01576	IPLRGAFANGRWDSQCHRFSNGAIACA	27	Sequence 11 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01577	IPLRGAFIAGRWDSQCHRFSNGAIACA	27	Sequence 12 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01578	IPLRGAFINARWDSQCHRFSNGAIACA	27	Sequence 13 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01579	IPLRGAFINGAWDSQCHRFSNGAIACA	27	Sequence 14 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01580	IPLRGAFINGRADSQCHRFSNGAIACA	27	Sequence 15 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01581	IPLRGAFINGRWASQCHRFSNGAIACA	27	Sequence 16 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01582	IPLRGAFINGRWDAQCHRFSNGAIACA	27	Sequence 17 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01583	IPLRGAFINGRWDSACHRFSNGAIACA	27	Sequence 18 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01584	IPLRGAFINGRWDSQAHRFSNGAIACA	27	Sequence 19 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01585	IPLRGAFINGRWDSQCARFSNGAIACA	27	Sequence 20 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01586	IPLRGAFINGRWDSQCHAFSNGAIACA	27	Sequence 21 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01587	IPLRGAFINGRWDSQCHRASNGAIACA	27	Sequence 22 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01588	IPLRGAFINGRWDSQCHRFANGAIACA	27	Sequence 23 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01589	IPLRGAFINGRWDSQCHRFSAGAIACA	27	Sequence 24 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01590	IPLRGAFINGRWDSQCHRFSNAAIACA	27	Sequence 25 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01591	IPLRGAFINGRWDSQCHRFSNGAAACA	27	Sequence 26 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01592	IPLRGAFINGRWDSQCHRFSNGAIAAA	27	Sequence 27 from Patent US 20190367567	Synthetic construct	H1N1	Patent Application	US 2019/0367567 A1	2019-12-05	WO 2018/102753 A1##EP 3548056 A1##US 2019/0367567 A1##EP 3548056 A4	Peptides and Uses for Managing Viral Infections	The peptide is useful for the prevention or treatment of viral infections such as influenza infections and exhibits no toxicity to human red blood cells.	"It has been discovered that certain peptides are useful for managing certain viral infections. Thus, this disclosure relates to the use of peptides reported herein for the prevention or treatment of viral infections such as influenza infections. In certain embodiments, this disclosure relates to peptides, variants, or derivatives having sequences disclosed herein and pharmaceutical compositions comprising the same."
DRAVP01593	VPKCCKPV	8	Sequence 11 from Patent US 7244710	Synthetic construct	"Herpesvirus,HIV"	Granted Patent	US 7244710 B2	2007-07-17	FR 1456903 A##ES 323291 A1##SU 622426 A3	Treatment Of Ophthalmic Infections Using Antimicrobial Peptides	"The peptide is formed by two PKV peptides which linked by a linker(disulfide bond between residues 4 and 5).The peptide could treat viral ophthalmic infection of the invention caused by Poxvirus, Herpesvirus, Adenovirus, Paramyxovirus and Human Immunodeficiency virus, especially Herpesvirus and Human Immunodedeficiency virus(HIV), the key species in Herpesvirus are Herpes simplex virus, Herpes zoster virus, Epstein-Barr virus, Cytomegalovirus.The possible mechanism of action is inhibiting HIV-p24 expression in HIV infected cells or HIV transcription."	"The present invention discloses a method of treating an ophthalmic infection by administering to a vertebrate inflicted with the ophthalmic infection an ophthalmologically effective amount of an antimicrobial peptide which is derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) and biologically functional equivalents thereof. Specifically, the antimicrobial peptides derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) include ¦Á-MSH (1¨C13) which is SYSMEHFRWGKPV, ¦Á-MSH (4¨C10) which is MEHFRWG, ¦Á-MSH (6¨C13) which is HFRWGKPV, ¦Á-MSH (11¨C13) which is KPV, and a KPV dimer. The ophthalmic infection can be caused by a microorganism which include a bacteria, a fungi or a virus. The vertebrate includes a bird and a mammal. The antimicrobial peptide has anti-bacterial, antifungal, and antiviral property and therefore can be administered at the onset of the ophthalmic infection before the microorganism causing the infection is determined as well as thereafter."
DRAVP01594	VPKCXKPV	8	Sequence 10 from Patent US 7244710	Synthetic construct	"Herpesvirus,HIV"	Granted Patent	US 7244710 B2	2007-07-17	FR 1456903 A##ES 323291 A1##SU 622426 A3	Treatment Of Ophthalmic Infections Using Antimicrobial Peptides	"The peptide is formed by two PKV peptides which linked by a linker(disulfide bond between residues 4 and 5).The peptide could treat viral ophthalmic infection of the invention caused by Poxvirus, Herpesvirus, Adenovirus, Paramyxovirus and Human Immunodeficiency virus, especially Herpesvirus and Human Immunodedeficiency virus(HIV), the key species in Herpesvirus are Herpes simplex virus, Herpes zoster virus, Epstein-Barr virus, Cytomegalovirus.The possible mechanism of action is inhibiting HIV-p24 expression in HIV infected cells or HIV transcription."	"The present invention discloses a method of treating an ophthalmic infection by administering to a vertebrate inflicted with the ophthalmic infection an ophthalmologically effective amount of an antimicrobial peptide which is derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) and biologically functional equivalents thereof. Specifically, the antimicrobial peptides derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) include ¦Á-MSH (1¨C13) which is SYSMEHFRWGKPV, ¦Á-MSH (4¨C10) which is MEHFRWG, ¦Á-MSH (6¨C13) which is HFRWGKPV, ¦Á-MSH (11¨C13) which is KPV, and a KPV dimer. The ophthalmic infection can be caused by a microorganism which include a bacteria, a fungi or a virus. The vertebrate includes a bird and a mammal. The antimicrobial peptide has anti-bacterial, antifungal, and antiviral property and therefore can be administered at the onset of the ophthalmic infection before the microorganism causing the infection is determined as well as thereafter."
DRAVP01595	VPKCCKPV	8	Sequence 9 from Patent US 7244710	Synthetic construct	"Herpesvirus,HIV"	Granted Patent	US 7244710 B2	2007-07-17	FR 1456903 A##ES 323291 A1##SU 622426 A3	Treatment Of Ophthalmic Infections Using Antimicrobial Peptides	"The peptide is formed by two PKV peptides which linked by a linker(disulfide bond between residues 4 and 5).The peptide could treat viral ophthalmic infection of the invention caused by Poxvirus, Herpesvirus, Adenovirus, Paramyxovirus and Human Immunodeficiency virus, especially Herpesvirus and Human Immunodedeficiency virus(HIV), the key species in Herpesvirus are Herpes simplex virus, Herpes zoster virus, Epstein-Barr virus, Cytomegalovirus.The possible mechanism of action is inhibiting HIV-p24 expression in HIV infected cells or HIV transcription."	"The present invention discloses a method of treating an ophthalmic infection by administering to a vertebrate inflicted with the ophthalmic infection an ophthalmologically effective amount of an antimicrobial peptide which is derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) and biologically functional equivalents thereof. Specifically, the antimicrobial peptides derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) include ¦Á-MSH (1¨C13) which is SYSMEHFRWGKPV, ¦Á-MSH (4¨C10) which is MEHFRWG, ¦Á-MSH (6¨C13) which is HFRWGKPV, ¦Á-MSH (11¨C13) which is KPV, and a KPV dimer. The ophthalmic infection can be caused by a microorganism which include a bacteria, a fungi or a virus. The vertebrate includes a bird and a mammal. The antimicrobial peptide has anti-bacterial, antifungal, and antiviral property and therefore can be administered at the onset of the ophthalmic infection before the microorganism causing the infection is determined as well as thereafter."
DRAVP01596	VPKCCKPV	8	Sequence 8 from Patent US 7244710	Synthetic construct	"Herpesvirus,HIV"	Granted Patent	US 7244710 B2	2007-07-17	FR 1456903 A##ES 323291 A1##SU 622426 A3	Treatment Of Ophthalmic Infections Using Antimicrobial Peptides	"The peptide is formed by two PKV peptides which linked by a linker(disulfide bond between residues 4 and 5), and the Cys at position 4 and 5 refers to Omocysteine.The peptide could treat viral ophthalmic infection of the invention caused by Poxvirus, Herpesvirus, Adenovirus, Paramyxovirus and Human Immunodeficiency virus, especially Herpesvirus and Human Immunodedeficiency virus(HIV), the key species in Herpesvirus are Herpes simplex virus, Herpes zoster virus, Epstein-Barr virus, Cytomegalovirus.The possible mechanism of action is inhibiting HIV-p24 expression in HIV infected cells or HIV transcription."	"The present invention discloses a method of treating an ophthalmic infection by administering to a vertebrate inflicted with the ophthalmic infection an ophthalmologically effective amount of an antimicrobial peptide which is derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) and biologically functional equivalents thereof. Specifically, the antimicrobial peptides derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) include ¦Á-MSH (1¨C13) which is SYSMEHFRWGKPV, ¦Á-MSH (4¨C10) which is MEHFRWG, ¦Á-MSH (6¨C13) which is HFRWGKPV, ¦Á-MSH (11¨C13) which is KPV, and a KPV dimer. The ophthalmic infection can be caused by a microorganism which include a bacteria, a fungi or a virus. The vertebrate includes a bird and a mammal. The antimicrobial peptide has anti-bacterial, antifungal, and antiviral property and therefore can be administered at the onset of the ophthalmic infection before the microorganism causing the infection is determined as well as thereafter."
DRAVP01597	VPKXXKPV	8	Sequence 7 from Patent US 7244710	Synthetic construct	"Herpesvirus,HIV"	Granted Patent	US 7244710 B2	2007-07-17	FR 1456903 A##ES 323291 A1##SU 622426 A3	Treatment Of Ophthalmic Infections Using Antimicrobial Peptides	"The peptide is formed by two PKV peptides which linked by a linker(disulfide bond between residues 4 and 5), the 'X' at position 4 and 5 indicates Penicillamine.The peptide could treat viral ophthalmic infection of the invention caused by Poxvirus, Herpesvirus, Adenovirus, Paramyxovirus and Human Immunodeficiency virus, especially Herpesvirus and Human Immunodedeficiency virus(HIV), the key species in Herpesvirus are Herpes simplex virus, Herpes zoster virus, Epstein-Barr virus, Cytomegalovirus.The possible mechanism of action is inhibiting HIV-p24 expression in HIV infected cells or HIV transcription."	"The present invention discloses a method of treating an ophthalmic infection by administering to a vertebrate inflicted with the ophthalmic infection an ophthalmologically effective amount of an antimicrobial peptide which is derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) and biologically functional equivalents thereof. Specifically, the antimicrobial peptides derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) include ¦Á-MSH (1¨C13) which is SYSMEHFRWGKPV, ¦Á-MSH (4¨C10) which is MEHFRWG, ¦Á-MSH (6¨C13) which is HFRWGKPV, ¦Á-MSH (11¨C13) which is KPV, and a KPV dimer. The ophthalmic infection can be caused by a microorganism which include a bacteria, a fungi or a virus. The vertebrate includes a bird and a mammal. The antimicrobial peptide has anti-bacterial, antifungal, and antiviral property and therefore can be administered at the onset of the ophthalmic infection before the microorganism causing the infection is determined as well as thereafter."
DRAVP01598	VPKXCKPV	8	Sequence 6 from Patent US 7244710	Synthetic construct	"Herpesvirus,HIV"	Granted Patent	US 7244710 B2	2007-07-17	FR 1456903 A##ES 323291 A1##SU 622426 A3	Treatment Of Ophthalmic Infections Using Antimicrobial Peptides	"The peptide is formed by two PKV peptides which linked by a linker(disulfide bond between residues 4 and 5), the 'X' at position 4 indicates Penicillamine.The peptide could treat viral ophthalmic infection of the invention caused by Poxvirus, Herpesvirus, Adenovirus, Paramyxovirus and Human Immunodeficiency virus, especially Herpesvirus and Human Immunodedeficiency virus(HIV), the key species in Herpesvirus are Herpes simplex virus, Herpes zoster virus, Epstein-Barr virus, Cytomegalovirus.The possible mechanism of action is inhibiting HIV-p24 expression in HIV infected cells or HIV transcription."	"The present invention discloses a method of treating an ophthalmic infection by administering to a vertebrate inflicted with the ophthalmic infection an ophthalmologically effective amount of an antimicrobial peptide which is derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) and biologically functional equivalents thereof. Specifically, the antimicrobial peptides derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) include ¦Á-MSH (1¨C13) which is SYSMEHFRWGKPV, ¦Á-MSH (4¨C10) which is MEHFRWG, ¦Á-MSH (6¨C13) which is HFRWGKPV, ¦Á-MSH (11¨C13) which is KPV, and a KPV dimer. The ophthalmic infection can be caused by a microorganism which include a bacteria, a fungi or a virus. The vertebrate includes a bird and a mammal. The antimicrobial peptide has anti-bacterial, antifungal, and antiviral property and therefore can be administered at the onset of the ophthalmic infection before the microorganism causing the infection is determined as well as thereafter."
DRAVP01599	CKPV	4	Sequence 5 from Patent US 7244710	Synthetic construct	"Herpesvirus,HIV"	Granted Patent	US 7244710 B2	2007-07-17	FR 1456903 A##ES 323291 A1##SU 622426 A3	Treatment Of Ophthalmic Infections Using Antimicrobial Peptides	"The peptide could treat viral ophthalmic infection of the invention caused by Poxvirus, Herpesvirus, Adenovirus, Paramyxovirus and Human Immunodeficiency virus, especially Herpesvirus and Human Immunodedeficiency virus(HIV), the key species in Herpesvirus are Herpes simplex virus, Herpes zoster virus, Epstein-Barr virus, Cytomegalovirus.The possible mechanism of action is inhibiting HIV-p24 expression in HIV infected cells or HIV transcription."	"The present invention discloses a method of treating an ophthalmic infection by administering to a vertebrate inflicted with the ophthalmic infection an ophthalmologically effective amount of an antimicrobial peptide which is derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) and biologically functional equivalents thereof. Specifically, the antimicrobial peptides derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) include ¦Á-MSH (1¨C13) which is SYSMEHFRWGKPV, ¦Á-MSH (4¨C10) which is MEHFRWG, ¦Á-MSH (6¨C13) which is HFRWGKPV, ¦Á-MSH (11¨C13) which is KPV, and a KPV dimer. The ophthalmic infection can be caused by a microorganism which include a bacteria, a fungi or a virus. The vertebrate includes a bird and a mammal. The antimicrobial peptide has anti-bacterial, antifungal, and antiviral property and therefore can be administered at the onset of the ophthalmic infection before the microorganism causing the infection is determined as well as thereafter."
DRAVP01600	VPKCCKPV	8	Sequence 4 from Patent US 7244710	Synthetic construct	"Herpesvirus,HIV"	Granted Patent	US 7244710 B2	2007-07-17	FR 1456903 A##ES 323291 A1##SU 622426 A3	Treatment Of Ophthalmic Infections Using Antimicrobial Peptides	"The peptide is formed by two PKV peptides which linked by a linker(disulfide bond between residues 4 and 5).The peptide could treat viral ophthalmic infection of the invention caused by Poxvirus, Herpesvirus, Adenovirus, Paramyxovirus and Human Immunodeficiency virus, especially Herpesvirus and Human Immunodedeficiency virus(HIV), the key species in Herpesvirus are Herpes simplex virus, Herpes zoster virus, Epstein-Barr virus, Cytomegalovirus.The possible mechanism of action is inhibiting HIV-p24 expression in HIV infected cells or HIV transcription."	"The present invention discloses a method of treating an ophthalmic infection by administering to a vertebrate inflicted with the ophthalmic infection an ophthalmologically effective amount of an antimicrobial peptide which is derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) and biologically functional equivalents thereof. Specifically, the antimicrobial peptides derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) include ¦Á-MSH (1¨C13) which is SYSMEHFRWGKPV, ¦Á-MSH (4¨C10) which is MEHFRWG, ¦Á-MSH (6¨C13) which is HFRWGKPV, ¦Á-MSH (11¨C13) which is KPV, and a KPV dimer. The ophthalmic infection can be caused by a microorganism which include a bacteria, a fungi or a virus. The vertebrate includes a bird and a mammal. The antimicrobial peptide has anti-bacterial, antifungal, and antiviral property and therefore can be administered at the onset of the ophthalmic infection before the microorganism causing the infection is determined as well as thereafter."
DRAVP01601	SYSMEHFRWGKPV	13	Sequence 3 from Patent US 7244710(¦Á-MSH [1-13])	Homo sapiens	"Herpesvirus,HIV"	Granted Patent	US 7244710 B2	2007-07-17	FR 1456903 A##ES 323291 A1##SU 622426 A3	Treatment Of Ophthalmic Infections Using Antimicrobial Peptides	"The peptide could treat viral ophthalmic infection of the invention caused by Poxvirus, Herpesvirus, Adenovirus, Paramyxovirus and Human Immunodeficiency virus, especially Herpesvirus and Human Immunodedeficiency virus(HIV), the key species in Herpesvirus are Herpes simplex virus, Herpes zoster virus, Epstein-Barr virus, Cytomegalovirus.The possible mechanism of action is inhibiting HIV-p24 expression in HIV infected cells or HIV transcription."	"The present invention discloses a method of treating an ophthalmic infection by administering to a vertebrate inflicted with the ophthalmic infection an ophthalmologically effective amount of an antimicrobial peptide which is derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) and biologically functional equivalents thereof. Specifically, the antimicrobial peptides derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) include ¦Á-MSH (1¨C13) which is SYSMEHFRWGKPV, ¦Á-MSH (4¨C10) which is MEHFRWG, ¦Á-MSH (6¨C13) which is HFRWGKPV, ¦Á-MSH (11¨C13) which is KPV, and a KPV dimer. The ophthalmic infection can be caused by a microorganism which include a bacteria, a fungi or a virus. The vertebrate includes a bird and a mammal. The antimicrobial peptide has anti-bacterial, antifungal, and antiviral property and therefore can be administered at the onset of the ophthalmic infection before the microorganism causing the infection is determined as well as thereafter."
DRAVP01602	HFRWGKPV	8	Sequence 2 from Patent US 7244710(¦Á-MSH [6-13])	Homo sapiens	"Herpesvirus,HIV"	Granted Patent	US 7244710 B2	2007-07-17	FR 1456903 A##ES 323291 A1##SU 622426 A3	Treatment Of Ophthalmic Infections Using Antimicrobial Peptides	"The peptide could treat viral ophthalmic infection of the invention caused by Poxvirus, Herpesvirus, Adenovirus, Paramyxovirus and Human Immunodeficiency virus, especially Herpesvirus and Human Immunodedeficiency virus(HIV), the key species in Herpesvirus are Herpes simplex virus, Herpes zoster virus, Epstein-Barr virus, Cytomegalovirus.The possible mechanism of action is inhibiting HIV-p24 expression in HIV infected cells or HIV transcription."	"The present invention discloses a method of treating an ophthalmic infection by administering to a vertebrate inflicted with the ophthalmic infection an ophthalmologically effective amount of an antimicrobial peptide which is derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) and biologically functional equivalents thereof. Specifically, the antimicrobial peptides derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) include ¦Á-MSH (1¨C13) which is SYSMEHFRWGKPV, ¦Á-MSH (4¨C10) which is MEHFRWG, ¦Á-MSH (6¨C13) which is HFRWGKPV, ¦Á-MSH (11¨C13) which is KPV, and a KPV dimer. The ophthalmic infection can be caused by a microorganism which include a bacteria, a fungi or a virus. The vertebrate includes a bird and a mammal. The antimicrobial peptide has anti-bacterial, antifungal, and antiviral property and therefore can be administered at the onset of the ophthalmic infection before the microorganism causing the infection is determined as well as thereafter."
DRAVP01603	MEHFRWG	7	Sequence 1 from Patent US 7244710(¦Á-MSH [4-10])	Homo sapiens	"Herpesvirus,HIV"	Granted Patent	US 7244710 B2	2007-07-17	FR 1456903 A##ES 323291 A1##SU 622426 A3	Treatment Of Ophthalmic Infections Using Antimicrobial Peptides	"The peptide could treat viral ophthalmic infection of the invention caused by Poxvirus, Herpesvirus, Adenovirus, Paramyxovirus and Human Immunodeficiency virus, especially Herpesvirus and Human Immunodedeficiency virus(HIV), the key species in Herpesvirus are Herpes simplex virus, Herpes zoster virus, Epstein-Barr virus, Cytomegalovirus.The possible mechanism of action is inhibiting HIV-p24 expression in HIV infected cells or HIV transcription."	"The present invention discloses a method of treating an ophthalmic infection by administering to a vertebrate inflicted with the ophthalmic infection an ophthalmologically effective amount of an antimicrobial peptide which is derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) and biologically functional equivalents thereof. Specifically, the antimicrobial peptides derived from alpha-melanocyte-stimulating hormone (¦Á-MSH) include ¦Á-MSH (1¨C13) which is SYSMEHFRWGKPV, ¦Á-MSH (4¨C10) which is MEHFRWG, ¦Á-MSH (6¨C13) which is HFRWGKPV, ¦Á-MSH (11¨C13) which is KPV, and a KPV dimer. The ophthalmic infection can be caused by a microorganism which include a bacteria, a fungi or a virus. The vertebrate includes a bird and a mammal. The antimicrobial peptide has anti-bacterial, antifungal, and antiviral property and therefore can be administered at the onset of the ophthalmic infection before the microorganism causing the infection is determined as well as thereafter."
DRAVP01604	GICRCICGRGICRCICGR	18	Sequence 1 from Patent US 2009/0264344  A1	Homo sapiens	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	The peptide is potently active against both X4 and R5 strains of HIV-1 by inhibiting virus replication. The mean IC50 value of RC-101 for the seven subtype B strains was <1.25 ¦Ìg/ml (<660 nM).	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01605	GICRCICGKGICRCICGR	18	Sequence 2 from Patent US 2009/0264344  A1(RC-101)	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	The peptide is potently active against both X4 and R5 strains of HIV-1 by inhibiting virus replication.	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01606	GICRCYCGRGICRCICGR	18	Sequence 3 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	The peptide is potently active against both X4 and R5 strains of HIV-1 by inhibiting virus replication.	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01607	GICRCICGRGICRCYCGR	18	Sequence 4 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	The peptide is potently active against both X4 and R5 strains of HIV-1 by inhibiting virus replication.	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01608	GYCRCICGRGICRCICGR	18	Sequence 5 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	The peptide is potently active against both X4 and R5 strains of HIV-1 by inhibiting virus replication.	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01609	GICRCICGRGYCRCICGR	18	Sequence 6 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	The peptide is potently active against both X4 and R5 strains of HIV-1 by inhibiting virus replication.	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01610	GICYCICGRGICRCICGR	18	Sequence 7 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	The peptide is potently active against both X4 and R5 strains of HIV-1 by inhibiting virus replication.	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01611	GICICICGYGICRCICGR	18	Sequence 8 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	The peptide is potently active against both X4 and R5 strains of HIV-1 by inhibiting virus replication.	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01612	GICICICGRGICYCICGR	18	Sequence 9 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	The peptide is potently active against both X4 and R5 strains of HIV-1 by inhibiting virus replication.	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01613	RGCICRCIGRGCICRCIG	18	Sequence 10 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	The peptide is potently active against both X4 and R5 strains of HIV-1 by inhibiting virus replication.	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01614	AQAEPLQARADEAAAQEQPGADDQEMAHAFTWHESAALPLSDSARGLRCICGRGICRLL	59	Sequence 12 from Patent US 2009/0264344  A1	Homo sapiens	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01615	MRIIALLAAILLVALQVRAGPLQARGDEAPGQEQRGPEDQDISISFAWDKSSALQVSGSTRGMVCSCRLVFCRRTELRVGNCLIGGVSFTYCCTRVD	97	Sequence 13 from Patent US 2009/0264344  A1(human defensin 4)	Homo sapiens	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01616	MRTFALLTAMLLLVALHAQAEARQARADEAAAQQQPGTDDQGMAHSFTWPENAALPLSESAKGLRCICTRGFCRLL	76	Sequence 15 from Patent US 2009/0264344  A1	Macaca mulatta	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01617	MRTFALLTAMLLLVALHAQAEARQARADEAAAQQQPGADDQGMAHSFTRPENAALPLSESARGLRCLCRRGVCQLL	76	Sequence 17 from Patent US 2009/0264344  A1	Macaca mulatta	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01618	RCICGRGIC	9	Sequence 19 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01619	RCLCGRGIC	9	Sequence 20 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01620	RCICRRGIC	9	Sequence 21 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01621	RCICTRGIC	9	Sequence 22 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01622	RCICVRGIC	9	Sequence 23 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01623	RCICGLGIC	9	Sequence 24 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01624	RCICGRGVC	9	Sequence 25 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01625	RCICGRGFC	9	Sequence 26 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01626	RCLCRRGVC	9	Sequence 27 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01627	RCLCTRGIC	9	Sequence 28 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01628	RCLCVRGIC	9	Sequence 29 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01629	RCLCGLGVC	9	Sequence 30 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01630	RCLCGRGVC	9	Sequence 31 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01631	RCLCGRGFC	9	Sequence 32 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01632	RCICRRGVC	9	Sequence 33 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01633	RCICRRGFC	9	Sequence 34 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01634	RCICTRGVC	9	Sequence 35 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01635	RCICTRGFC	9	Sequence 36 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01636	RCICTLGIC	9	Sequence 37 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01637	RCICVLGFC	9	Sequence 38 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01638	RCICRLGIC	9	Sequence 39 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01639	RCICVRGVC	9	Sequence 40 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01640	RCICGRGFC	9	Sequence 41 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01641	RCICGLGFC	9	Sequence 42 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01642	RCICGLGVC	9	Sequence 43 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01643	RCLCRLGIC	9	Sequence 44 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01644	RCLCRRGVC	9	Sequence 45 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01645	RCLCRRGFC	9	Sequence 46 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01646	RCLCTLGIC	9	Sequence 47 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01647	RCLCTRGVC	9	Sequence 48 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01648	RCLCTRGFC	9	Sequence 49 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01649	RCLCVLGIC	9	Sequence 50 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01650	RCLCVRGVC	9	Sequence 51 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01651	RCICGRGIC	9	Sequence 52 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01652	RCICRLGVC	9	Sequence 53 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01653	RCICRLGFC	9	Sequence 54 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01654	RCICTLGVC	9	Sequence 55 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01655	RCICTLGFC	9	Sequence 56 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01656	RCICVLGVC	9	Sequence 57 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01657	RCICVLGFC	9	Sequence 58 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01658	RCLCGLGVC	9	Sequence 59 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01659	RCLCGLGIC	9	Sequence 60 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01660	RCLCTLGVC	9	Sequence 61 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01661	RCLCTLGIC	9	Sequence 62 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01662	RCLCVLGVC	9	Sequence 63 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01663	RCLCVLGIC	9	Sequence 64 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01756	CCGGIEKKIEEIEKKIEEIEKKIEEIEKLLQLTVWGIKALAAAIA	45	Sequence 9 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01755	IEKKIEEIEKKIEEIEKKIEEIEKLLQLTVWGIKALAAAIA	41	Sequence 8 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01754	CCGGIEKKIEEIEKKIEEIEKKIEEIEKLLQLTVWGIKQLQARIL	45	Sequence 7 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01753	IEKKIEEIEKKIEEIEKKIEEIEKLLQLTVWGIKQLQARIL	41	Sequence 6 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01752	CCGGIKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKALAAAIA	45	Sequence 5 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01751	IKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKALAAAIA	41	Sequence 4 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01664	RCICGRRIC	9	Sequence 74 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01665	RCLCGRRIC	9	Sequence 75 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01666	RCICRRRIC	9	Sequence 76 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01667	RCICTRRIC	9	Sequence 77 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01668	RCICVRRIC	9	Sequence 78 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01669	RCICGLRIC	9	Sequence 79 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01670	RCICGRRVC	9	Sequence 80 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01671	RCICGRRFC	9	Sequence 81 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01672	RCLCRRRVC	9	Sequence 82 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01673	RCLCTRRIC	9	Sequence 83 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01674	RCLCVRRIC	9	Sequence 84 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01675	RCLCGLRVC	9	Sequence 85 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01676	RCLCGRRVC	9	Sequence 86 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01677	RCLCGRRFC	9	Sequence 87 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01678	RCICRRRVC	9	Sequence 88 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01679	RCICRRRFC	9	Sequence 89 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01680	RCICTRRVC	9	Sequence 90 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01681	RCICTRRFC	9	Sequence 91 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01682	RCICTLRIC	9	Sequence 92 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01683	RCICVLRFC	9	Sequence 93 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01684	RCICRLRIC	9	Sequence 94 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01685	RCICVRRVC	9	Sequence 95 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01686	RCICGRRFC	9	Sequence 96 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01687	RCICGLRFC	9	Sequence 97 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01688	RCICGLRVC	9	Sequence 98 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01689	RCLCRLRIC	9	Sequence 99 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01690	RCLCRRRVC	9	Sequence 100 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01691	RCLCRRRFC	9	Sequence 101 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01692	RCLCTLRIC	9	Sequence 102 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01693	RCLCGRRVC	9	Sequence 103 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01694	RCLCTRRFC	9	Sequence 104 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01695	RCLCVLRIC	9	Sequence 105 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01696	RCLCVRRVC	9	Sequence 106 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01697	RCICGRRIC	9	Sequence 107 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01698	RCICRLRVC	9	Sequence 108 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01699	RCICRLRFC	9	Sequence 109 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01700	RCICTLRVC	9	Sequence 110 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01701	RCICTLRFC	9	Sequence 111 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01702	RCICVLRVC	9	Sequence 112 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01703	RCICVLRFC	9	Sequence 113 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01704	RCLCGLRVC	9	Sequence 114 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01705	RCLCGLRIC	9	Sequence 115 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01706	RCLCTLRVC	9	Sequence 116 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01707	RCLCTLRIC	9	Sequence 117 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01708	RCLCVLRVC	9	Sequence 118 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01709	RCLCVLRIC	9	Sequence 119 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01749	CCGGIKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQLQARIL	45	Sequence 2 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide exihibits antiviral activity as a fusion inhibitor(HIV HXB2:IC50=0.04 nM; HIV Bal:IC50=0.34 nM;HIV 89.6:IC50=8 nM;HIV SHIV89.6p:IC50=6.9 Nm;HIV MN-1:IC50=0.9 nM;HIV NL43:IC50=0.1 nM).The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01710	GICRCICGKGICRCYCGR	18	Sequence 126 from Patent US 2009/0264344  A1(RC101/103 hybrid)	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01711	GICKCICGKGICKCICGR	18	Sequence 127 from Patent US 2009/0264344  A1(K Retrocyclin-1)	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01712	GICRCICGKRICRCICGR	18	Sequence 128 from Patent US 2009/0264344  A1(Retrocyclin 2A)	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01713	GICRCICGKKICRCICGR	18	Sequence 129 from Patent US 2009/0264344  A1(Retrocyclin 2B)	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01714	GICRCICGRKICRCICGR	18	Sequence 130 from Patent US 2009/0264344  A1(Retrocyclin 2C)	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01715	GICRCICGRRICKCICGR	18	Sequence 131 from Patent US 2009/0264344  A1(Retrocyclin 2D)	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01716	GICKCICGRRICRCICGR	18	Sequence 132 from Patent US 2009/0264344  A1(Retrocyclin 2E)	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01717	GICRCICGRRICRCICGK	18	Sequence 133 from Patent US 2009/0264344  A1(Retrocyclin 2F)	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01718	GVCRCICGRGVCRCICRR	18	Sequence 134 from Patent US 2009/0264344  A1	Orangutan	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01719	GVCRCICGRGVCRCICGR	18	Sequence 135 from Patent US 2009/0264344  A1	Orangutan	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01720	RXICGXXIC	9	Sequence 136 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The 'X' at position 2 and 6 indicates Arg or Lys, and the 'X' at position 7 indicates Arg, Lys or Gly.The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01721	GICYCICGKGICRCICGR	18	Sequence 137 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01722	GICRCICGRYICRCICGR	18	Sequence 138 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01723	RYICRCICGRGICRCICG	18	Sequence 139 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01724	GICRCICGRRICRCICGR	18	Sequence 140 from Patent US 2009/0264344  A1	Synthetic construct	"HIV-1,HSV-1,HSV-2"	Patent Application	US 2009/0264344 A1	2009-10-22	US 2005/0272645 A1##WO 2006/052637 A1##US 7314858 B2##US 2009/0264344 A1##US 7718610 B2	Retrocyclins: Antiviral and Antimicrobial Peptides	"The peptide has potent activity against viruses, e.g. enveloped viruses such as retroviruses.It is nonhemolytic and generally exhibits little or no in vitro cytotoxicity."	"Retrocyclin peptides are small antimicrobial agents with potent activity against bacteria and viruses. The peptides are nonhemolytic, and exhibit minimal in vitro cytotoxicity. A pharmaceutical composition comprising retrocyclin as an active agent is administered therapeutically to a patient suffering from a bacterial and/or viral infection, or to an individual facing exposure to a bacterial and/or viral infection, especially one caused by the HIV-1 retrovirus or other sexually-transmitted pathogens."
DRAVP01725	RWRQTWSGPGTTKRFPETVLARCVKYTEIH	30	Sequence 1 from Patent US 8080633	Homo sapiens	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01726	NTRKSHIGPGRAFYTTGIIGDIRQAH	26	Sequence 2 from Patent US 8080633	Human immunodeficiency virus(HIV gp120 299-324)	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01727	TRPNNNTRKSIIGPGRAFYTTGQIIGDIRQAH	32	Sequence 3 from Patent US 8080633	Human immunodeficiency virus(HIV sub B)	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01728	TRPNNNTRRSIRIGPGQAFYATGDIIGDIRQAH	33	Sequence 4 from Patent US 8080633	Human immunodeficiency virus(HIV sub A)	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01729	TRPNNNTRKSIRIGPGQTFYATGDIIGDIRQAH	33	Sequence 5 from Patent US 8080633	Human immunodeficiency virus(HIV sub C)	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01730	TRPYNRQRTPIGLGQALYTTRYTTRIIGQAY	31	Sequence 6 from Patent US 8080633	Human immunodeficiency virus(HIV sub D)	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01731	TRPSNNTRTSRIGPGRVFYKTGDIIGDIRKAY	32	Sequence 7 from Patent US 8080633	Human immunodeficiency virus(HIV sub E)	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01732	TRPGNNTGGQVQIGPAMTFYNIEKIVGDRQAY	32	Sequence 8 from Patent US 8080633	Human immunodeficiency virus(HIV subgroup N)	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01733	RPGVQEIIGPMAWYSMGLNNSRAY	24	Sequence 9 from Patent US 8080633	Human immunodeficiency virus(HIV subgroup O)	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01734	RPGNNTRGQIGPGMTFYNIENIVGDTRA	28	Sequence 10 from Patent US 8080633	Simian immunodeficiency virus(SIV cpz)	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01735	KRPGNKTVVPITLMSGLVFHSQPINRPRQAW	31	Sequence 11 from Patent US 8080633	Human immunodeficiency virus(HIV-2)	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01736	RWRQTWSGPGTTKRFPETVLARCVKYTEIH	30	Sequence 12 from Patent US 8080633	Homo sapiens	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01737	RQTWSGPGTTKRFPETVLARCVKYTEIH	28	Sequence 13 from Patent US 8080633	Homo sapiens	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01738	RWRQTWSGPGTTK	13	Sequence 14 from Patent US 8080633	Homo sapiens	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01739	SGPGTTKRFPETVLARCVKYTEIH	24	Sequence 15 from Patent US 8080633	Homo sapiens	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01740	RWRQQWSGPGTTKRFPETVLARCVKYTEIH	30	Sequence 16 from Patent US 8080633	Homo sapiens	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01741	RQQWSGPGTTKRFPETVLARCVKYTEIH	28	Sequence 17 from Patent US 8080633	Homo sapiens	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01742	GPGTTK	6	Sequence 18 from Patent US 8080633	Homo sapiens	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01743	RWRQQWSGPGTTKRFPETVLARCVKYTEIH	30	Sequence 19 from Patent US 8080633	Homo sapiens	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01744	NTRKSIIGPGRAFYTTGQIIGDIRQAH	27	Sequence 20 from Patent US 8080633	Human immunodeficiency virus(HIV-1 subtype B gp120	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01745	SGPGTTKRFPETVLACVKYTEIH	23	Sequence 21 from Patent US 8080633	Homo sapiens	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01746	KNIYRPDKFLQCVKNPEDSSCTSEI	25	Sequence 22 from Patent US 8080633	Homo sapiens	HIV	Granted Patent	US 8080633 B2	2011-12-20	WO 2003/091275 A2##AU 2003/241103 A8##AU 2003/241103 A1##US 2004/0116653 A1##US 8030444 B2##US 2009/0170764 A1##US 7553926 B2##US 2009/0088381 A1	Antiviral compositions comprising a multiple branched peptide construct containing human CD38 leukocyte surface antigen polypeptides		Peptides representing sequences from region 45-74 of the human CD38 leukocyte surface antigen (SEQ ID NO:1) are provided which may be used to inhibit or prevent transmission or replication of the HIV virus. The peptides have from 13 to 30 amino acids and include the amino acid sequence GPGTTK (SEQ ID NO:18) for topical application to inhibit or prevent transmission of the HIV virus.
DRAVP01750	GKGIKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQLQARIL	44	Sequence 3 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01748	IKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQLQARIL	41	Sequence 1 from Patent US 7811577 B2 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide exihibits antiviral activity as a fusion inhibitor(HIV HXB2:IC50=1.7 nM; HIV Bal:IC50=3.2 nM).The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01757	IKKEIEAIKKEQEAIKKKIEAIEKEIEAQQHLLQLTVWGIKQLQARIL	48	Sequence 10 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01758	GGIKKEIEAIKKEQEAIKKKIEAIEKEIEAQQHLLQLTVWGIKQLQARIL	50	Sequence 11 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide exihibits antiviral activity as a fusion inhibitor(HIV HXB2:IC50=2.173 nM).	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01759	GCCGGIKKEIEAIKKEQEAIKKKIEAIEKEIEAQQHLLQLTVWGIKQLQARIL	53	Sequence 12 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide exihibits antiviral activity as a fusion inhibitor(HIV HXB2:IC50=0.316 nM).	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01760	CCGGIKKEIEAIKKEQEAIKKKIEAIEKEIEAQQHLLQLTVWGIKQLQARIL	52	Sequence 13 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01761	IEKKIEEIEKKIEEIEKKIEEIEEKIEAQQHLLQLTVWGIKQLQARIL	48	Sequence 14 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01762	CCGGIEKKIEEIEKKIEEIEKKIEEIEEKIEAQQHLLQLTVWGIKQLQARIL	52	Sequence 15 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01763	IKKEIEAIKKEQEAIKKKIEAIEKEISGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARIL	62	Sequence 16 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01764	GKGIKKEIEAIKKEQEAIKKKIEAIEKEISGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARIL	65	Sequence 17 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01765	CCGGIKKEIEAIKKEQEAIKKKIEAIEKEISGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARIL	66	Sequence 18 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01766	IEKKIEEIEKKIEEIEKKIEEIEEKISGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARIL	62	Sequence 19 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01767	CCGGIKKKIEAIEKLLQLTVWGIKQLQARIL	31	Sequence 20 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01768	SGGCCGGIKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQLQARIL	48	Sequence 21 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01769	IKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWDIKQLQARIL	41	Sequence 22 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01770	RMKQIEDKIEEIESKQKKIENEIARIKKLLQLTVWGIKQLQARIL	45	Sequence 23 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01771	RMKQIEDKIEEIESKQKKIENEIARIKKLIEAQQHLLQLTVWGIKQLQARIL	52	Sequence 24 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01772	RMKQIEDKIEEIESKQKKIENEIARIKKLISGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARIL	66	Sequence 25 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01773	CCGGRMKQIEDKIEEIESKQKKIENEIARIKKLLQLTVWGIKQLQARIL	49	Sequence 26 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01774	CCGGRMKQIEDKIEEIESKQKKIENEIARIKKLLQLTVWGIKALAAAIA	49	Sequence 27 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01775	CCGG	4	Sequence 28 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01776	YGGIEKKIEAIEKKIEAIEKKIEAIEKKIEA	31	Sequence 29 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01777	RMKQIEDKIEEILSKQYHIENEIARIKKLIGER	33	Sequence 30 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01778	IKKEIEAIKKEQEAIKKKIEAIEK	24	Sequence 31 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01779	IEKKIEEIEKKIEEIEKKIEEIEK	24	Sequence 32 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01780	IEKKIEA	7	Sequence 33 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01781	IEKKIEE	7	Sequence 34 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01782	RMKQIEDKIEEIESKQKKIENEIARIKKL	29	Sequence 35 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01783	KQKKIENEIAAIKKL	15	Sequence 36 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01784	KIKKIENEIARIKKL	15	Sequence 37 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01785	KIEEIESKQKKIENEIARIKKL	22	Sequence 38 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01786	KIEEIESKIKKIENEIARIKK	21	Sequence 39 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01787	IKKEIEAIKKEQEAIKK	17	Sequence 40 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01788	IKKEIEAIKKEQEAIKKLLQLTVWGIKQLQARIL	34	Sequence 41 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01789	CCGGIKKEIEAIKKEQEAIKKLLQLTVWGIKQLQARIL	38	Sequence 42 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01790	IKKEIEAIKKEQEAIKKLLQLTVWGIKQLQARILGGCC	38	Sequence 43 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01791	LLQLTVWGIKQLQARIL	17	Sequence 44 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01792	IKKKIEAIEK	10	Sequence 45 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01793	IEAQQHLLQLTVWGIKQLQARIL	23	Sequence 48 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01794	AVERYLK	7	Sequence 49 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01795	LLQLTVWGIKQLQARILAVERYLK	24	Sequence 50 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01796	IEAQQHLLQLTVWGIKQLQARILAVERYLK	30	Sequence 51 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01797	SGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLK	43	Sequence 52 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01798	ARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLK	48	Sequence 53 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01799	IKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQLQARILAVERYLK	48	Sequence 54 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01800	IEKKIEEIEKKIEEIEKKIEEIEEKLLQLTVWGIKQLQARILAVERYLK	49	Sequence 55 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01801	RMKQIEDKIEEIESKQKKIENEIARIKKLLQLTVWGIKQLQARILAVERYLK	52	Sequence 56 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01802	IKKEIEAIKKEQEAIKKEIEAQQHLLQLTVWGIKQLQARIL	41	Sequence 57 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01803	IKKEIEAIKKEQEAIKKEISGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARIL	55	Sequence 58 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01804	IKKEIEAIKKEQEAIKKLLQLTVWGIKQLQARILAVERYLK	41	Sequence 59 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01805	LLQLTVWGIKALAAAIA	17	Sequence 60 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01806	CCGGIKKEIEAIKKEQEAIKKLLQLTVWGIKALAAAIA	38	Sequence 61 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01807	AGIVQQQQQLLDVVKRQQELLRLTVWGTKNLQTRVS	36	Sequence 62 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01808	QSLANATAAQQNVLEATYAMVQHVAKGVRILEARVA	36	Sequence 63 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01809	QTLANATAAQQDALEATYAMVQHVAKGVRILEARVA	36	Sequence 64 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01810	ATHQETIEKVTEALKINNLRLVTLEHQVLVIGLKVE	36	Sequence 65 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01811	NHTFEVENSTLNGMDLIERQIKILYAMILQTHADVQ	36	Sequence 66 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01812	ERVVQNVSYIAQTQDQFTHLFRNINNRLNVLHRRVS	36	Sequence 67 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01813	GCCGGIKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQLQARIL	46	Sequence 68 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01814	GCCGGIEKKIEEIEKKIEEIEKKIEEIEKLLQLTVWGIKQLQARIL	46	Sequence 69 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01815	GCCGGIKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKALAAAIA	46	Sequence 70 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01816	GCCGGIEKKIEEIEKKIEEIEKKIEEIEKLLQLTVWGIKALAAAIA	46	Sequence 71 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01817	IKKEIEAIKKEQEAIKKKIEAIEKALQLTVWGIKQLQARIL	41	Sequence 72 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01818	IKKEIEAIKKEQEAIKKKIEAIEKLLALTVWGIKQLQARIL	41	Sequence 73 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01819	IKKEIEAIKKEQEAIKKKIEAIEKLLQATVWGIKQLQARIL	41	Sequence 74 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01820	IKKEIEAIKKEQEAIKKKIEAIEKLLQLTAWGIKQLQARIL	41	Sequence 75 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01821	IKKEIEAIKKEQEAIKKKIEAIEKLLQLTVAGIKQLQARIL	41	Sequence 76 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01822	IKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIAQLQARIL	41	Sequence 77 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01823	IKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKALQARIL	41	Sequence 78 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01824	IKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQLAARIL	41	Sequence 79 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01825	IKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQLQAAIL	41	Sequence 80 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01826	IKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQLQARIA	41	Sequence 81 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01827	GGCC	4	Sequence 82 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01828	IKKKIEAIEKLLQLTVWGIKQLQARILGGCC	31	Sequence 83 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01829	ASQLL	5	Sequence 84 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01830	LIQLIVWGIKQIQARIL	17	Sequence 85 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01831	IKKKIEAIEKLIQLIVWGIKQIQARIL	27	Sequence 86 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01832	CCGGIKKKIEAIEKLIQLIVWGIKQIQARIL	31	Sequence 87 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01833	IKKKIEAIEKLIQLIVWGIKQIQARILGGCC	31	Sequence 88 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01834	IKKEIEAIKKEQEAIKKLIQLIVWGIKQIQARIL	34	Sequence 89 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01835	CCGGIKKEIEAIKKEQEAIKKLIQLIVWGIKQIQARIL	38	Sequence 90 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01836	IKKEIEAIKKEQEAIKKLIQLIVWGIKQIQARILGGCC	38	Sequence 91 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01837	IKKKIEAIEKLLQLTVWGIKQLQARILAVERYLK	34	Sequence 92 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01838	CCGGLLQLTVWGIKQLQARILAIKKEIEAIKKEQEAIKKKIEAI	44	Sequence 93 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01839	LLQLTVWGIKQLQARILAIKKEIEAIKKEQEAIKKKIEAI	40	Sequence 94 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01840	CCGGIKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQLQ	41	Sequence 95 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01841	CCGGIKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQIKKEIEAI	47	Sequence 96 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01842	IEKKIEAIEKKIEAIEKKIEAIEKLLQLTVWGIKQLQARIL	41	Sequence 97 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01843	CCGGIEKKIEAIEKKIEAIEKKIEAIEKLLQLTVWGIKQLQARIL	45	Sequence 98 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01844	IEKKIEAIEKKIEAIEKLLQLTVWGIKQLQARIL	34	Sequence 99 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01845	CCGGIEKKIEAIEKKIEAIEKLLQLTVWGIKQLQARIL	38	Sequence 100 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01846	IEKKIEAIEKLLQLTVWGIKQLQARIL	27	Sequence 101 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01847	CCGGIEKKIEAIEKLLQLTVWGIKQLQARIL	31	Sequence 102 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01848	CCCGGIKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQLQARIL	46	Sequence 103 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01849	GGGIKKEIEAIKKEQEAIKKKIEAIEKLLQLTVWGIKQLQARIL	44	Sequence 104 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01850	CCCGGIEKKIEAIEKKIEAIEKLLQLTVWGIKQLQARIL	39	Sequence 105 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01851	GGGIEKKIEAIEKKIEAIEKLLQLTVWGIKQLQARIL	37	Sequence 106 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01852	IEEKIEEIEE	10	Sequence 107 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01853	IEEKIEEIEELLQLTVWGIKQLQARIL	27	Sequence 108 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01854	CCGGIEEKIEEIEELLQLTVWGIKQLQARIL	31	Sequence 109 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01855	GGGIEEKIEEIEELLQLTVWGIKQLQARIL	30	Sequence 110 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01856	CCCGGIEEKIEEIEELLQLTVWGIKQLQARIL	32	Sequence 111 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01857	IEKKIEAIEKKIEAIEKKIEAIEK	24	Sequence 112 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01858	IEKKIEAIEK	10	Sequence 113 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01859	IEKKIEEIEKKIEEIEK	17	Sequence 114 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01860	IEKKIEEIEKKIEEIEKLLQLTVWGIKQLQARIL	34	Sequence 115 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01861	CCGGIEKKIEEIEKKIEEIEKLLQLTVWGIKQLQARIL	38	Sequence 116 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01862	IEKKIEEIEKKIEEIEKLLQLTVWGIKQLQARILGGCC	38	Sequence 117 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01863	IEKKIEEIEEKIEEIEKLLQLTVWGIKQLQARIL	34	Sequence 118 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01864	IEKKIEEIEEKIEEIEK	17	Sequence 119 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	No comments found in patent	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01865	CCGGIEKKIEEIEEKIEEIEKLLQLTVWGIKQLQARIL	38	Sequence 120 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01866	GGGIEKKIEEIEKKIEEIEKKIEEIEKLLQLTVWGIKQLQARIL	44	Sequence 121 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01867	CCCGGIEKKIEEIEKKIEEIEKKIEEIEKLLQLTVWGIKQLQARIL	46	Sequence 122 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01868	GGGIEKKIEEIEEKIEEIEKLLQLTVWGIKQLQARIL	37	Sequence 123 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01869	CCCGGIEKKIEEIEEKIEEIEKLLQLTVWGIKQLQARIL	39	Sequence 124 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01870	GGGIEKKIEEIEKKIEEIEKLLQLTVWGIKQLQARIL	37	Sequence 125 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01871	CCCGGIEKKIEEIEKKIEEIEKLLQLTVWGIKQLQARIL	39	Sequence 126 from Patent US 7811577 B2	Synthetic construct	HIV	Granted Patent	US 7811577 B2	2010-12-12	WO 2005/118886 A2##AU 2005/250430 A1##CA 2567030 A1##WO 2005/118886 A3##EP 1755667 A2##CN 1968710 A##US 2007/0224212 A1##JP 2008501028 A##EP 1755667 A4##US 7811577 B2##EP 2354153 A2##AU 2005/250430 B2	Covalently stabilized chimeric coiled-coil HIV gp41 N-peptides with improved antiviral activity	The peptide was modified with acetyl N-terminus and amide C-terminus.	"Methods of covalently-stabilizing alpha-helical, chimeric peptides constrained within a homotrimeric or heterotrimeric coiled-coil structure are disclosed. The coiled-coil structures made by the methods disclosed within this specification mimic all or a portion of the internal, trimeric coiled-coil motif contained within the fusogenic conformation of an enveloped virus membrane-fusion protein, particularly the internal coiled-coil domain of the HIV gp41 ectodomain. The HIV-derived, chimeric peptides disclosed comprise a non-HIV, soluble, trimeric form of a coiled-coil fused in helical phase to all or a portion of the N-helix of HIV gp41 and are covalently-stabilized in a homotrimeric or heterotrimeric coiled-coil structure through the formation of disulfide or chemoselective bonds between said peptides. The covalently-stabilized, HIV-derived, homotrimeric or heterotrimeric coiled-coil structures made by the methods disclosed herein represent a close mimetic of a HIV gp41 fusion intermediate and are potent inhibitors of HIV infectivity. These HIV-derived chimeric peptides may provide for therapeutic treatment against HIV infection by inhibiting the virus-host cell membrane fusion process."
DRAVP01872	KETWETWWTE	10	Sequence 1 from Patent US 7790171 B1	Synthetic construct(residues 395-404 of HIV-1 BH10	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01873	GALFLGFLGAAGSTMGAWSQPKSKRKV	27	Sequence 2 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01874	GFLGAA	6	Sequence 3 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01875	GFLGAAGSTMGAWSQKETWETWWTE	25	Sequence 4 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01876	RGTKALTEVIPLTED	15	Sequence 5 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01877	GALFLGFLGAAKETWETWWTE	21	Sequence 6 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01878	KETWEAWWTE	10	Sequence 7 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01879	KETWEAWWME	10	Sequence 8 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01880	KETWETWWIE	10	Sequence 9 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01881	KETWETWWAE	10	Sequence 10 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01882	REIWEQWWDN	10	Sequence 11 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01883	RETWDQWWTD	10	Sequence 12 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01884	KETWEXWWTX	10	Sequence 13 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	"The 'X' at position 6 indicates Thr or Ala, and the 'X' at position 10 indicates Glu or Asp."	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01885	KETWEXWWME	10	Sequence 14 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	The 'X' at position 6 indicates Thr or Ala.	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01886	KETWEAWWTD	10	Sequence 15 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01887	KETWEXWWXX	10	Sequence 16 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	"The 'X' at position 6 indicates Thr or Ala, the 'X' at position 10 indicates Glu or Asp,and the 'X' at position 9 indicates Thr,Ala,Val or Ile."	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01888	KETWDTWWTE	10	Sequence 17 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01889	KETWEVWWTE	10	Sequence 18 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01890	RETWETWWAD	10	Sequence 19 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	No comments found in patent	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01891	RXXWEQWWDX	10	Sequence 20 from Patent US 7790171 B1	Synthetic construct	HIV	Granted Patent	US 7790171 B1	2010-09-07	WO 2002/015661 A2##AU 2001/092153 A##WO 2002/015661 A8##WO 2002/015661 A3##EP 1311538 A2##EP 1311538 B1##AT 420103 T##DE 60137340 D1##US 7790171 B1##US 2011/0064793 A1	Antiviral peptides obtained from the tryptophan-rich hydrophobic cluster of the HIV-1 reverse transcriptase	"The 'X' at position 3 indicates Thr,Val or Ile, the 'X' at position 2 indicates Glu or Asp,and the 'X' at position 10 indicates Asn or Asp."	"The invention is drawn to a novel class of drugs directed against HIV, comprising a peptide or analog comprising a decapeptide, said decapeptide containing (from N-terminus to the C-terminus) a basic amino acid in position 1, an acidic amino acid in positions 2 and 5, and a tryptophan in positions 4, 7, and 8, and to a method of treatment of HIV infections, in particular multidrug-resistant HIV infections."
DRAVP01892	YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 1 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01893	NNLLRAIEAQQHLLQLTVWQIKQLQARILAVERYLKDQ	38	Sequence 2 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01894	YTNTIYTLLEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 3 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01895	YTGIIYNLLEESQNQQEKNEQELLELDKWANLWNWF	36	Sequence 4 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01896	YTSLIYSLLEKSQTQQEKNEQELLELDKWASLWNWF	36	Sequence 5 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01897	LEANISKSLEQAQIQQEKNMYELQKLNSWDIFGNWF	36	Sequence 6 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01898	LEANISQSLEQAQIQQEKNMYELQKLNSWDVFTNWL	36	Sequence 7 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01899	CGGNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	41	Sequence 8 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01900	QQLLDVVKRQQEMLRLTVWGTKNLQARVTAIEKYLKDQ	38	Sequence 9 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01901	YTSVITIELSNIKENKCNGAKVKLIKQELDKYKNAVTELQLLMQST	46	Sequence 10 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01902	ASGVAVSKVLHLEGEVNKIALLSTNKAVVSLSNGVSVLTSKVLDLKNYIDKQLL	54	Sequence 11 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01903	GEPIINFYDPLVFPSDEFDASISQVNEKINQSLAFIRKSDELLHNVNAGKSTT	53	Sequence 12 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01904	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	48	Sequence 13 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01905	YTSVITIELSNIKENKCNGDAKVKLIKQELDKYK	34	Sequence 14 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01906	TSVITIELSNIKENKCNGDAKVKLIKQELDKYKN	34	Sequence 15 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01907	VITIELSNIKENKCNGDAKVKLIKQELDKYKNAV	34	Sequence 16 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01908	VITIELSNIKENKMNGDAKVKLIKQELDKYKNAV	34	Sequence 17 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01909	VAVSKVLHLEGEVNKIALLSTNKAVVSLSNGVS	33	Sequence 18 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01910	AVSKVLHLEGEVNKIALLSTNKAVVSLSNGVSV	33	Sequence 19 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01911	VSKVLHLEGEVNKIALLSTNKAVVSLSNGVSVL	33	Sequence 20 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01912	SKVLHLEGEVNKIALLSTNKAVVSLSNGVSVLT	33	Sequence 21 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01913	KVLHLEGEVNKIALLSTNKAVVSLSNGVSVLTS	33	Sequence 22 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01914	LEGEVNKIALLSTNKAVVSLSNGVSVLTSKVLD	33	Sequence 23 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01915	GEVNKIALLSTNKAVVSLSNGVSVLTSKVLDLK	33	Sequence 24 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01916	EVNKIALLSTNKAVVSLSNGVSVLTSKVLDLKN	33	Sequence 25 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01917	VNKIALLSTNKAVVSLSNGVSVLTSKVLDLKNY	33	Sequence 26 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01918	NKIALLSTNKAVVSLSNGVSVLTSKVLDLKNYI	33	Sequence 27 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01919	KIALLSTNKAVVSLSNGVSVLTSKVLDLKNYID	33	Sequence 28 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01920	IALLSTNKAVVSLSNGVSVLTSKVLDLKNYIDK	33	Sequence 29 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01921	ALLSTNKAVVSLSNGVSVLTSKVLDLKNYIDKQ	33	Sequence 30 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01922	GTIALGVATSAQITAAVALVEAKQARSDIEKLKEAIRDTNKAVQSVQSSIGNLIVAIKSVQDYVNKEIVP	70	Sequence 31 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01923	YTPNDITLNNSVALDPIDISIELNKAKSDLEESKEWIRRSNQKLDSIGNWHQSSTT	56	Sequence 32 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01924	TLNNSVALDPIDISIELNKAKSDLEESKEWIRRSN	35	Sequence 33 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01925	LNNSVALDPIDISIELNKAKSDLEESKEWIRRSNQ	35	Sequence 34 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01926	NNSVALDPIDISIELNKAKSDLEESKEWIRRSNQK	35	Sequence 35 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01927	NSVALDPIDISIELNKAKSDLEESKEWIRRSNQKL	35	Sequence 36 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01928	SVALDPIDISIELNKAKSDLEESKEWIRRSNQKLD	35	Sequence 37 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01929	VALDPIDISIELNKAKSDLEESKEWIRRSNQKLDS	35	Sequence 38 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01930	ALDPIDISIELNKAKSDLEESKEWIRRSNQKLDSI	35	Sequence 39 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01931	LDPIDISIELNKAKSDLEESKEWIRRSNQKLDSIG	35	Sequence 40 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01932	DPIDISIELNKAKSDLEESKEWIRRSNQKLDSIGN	35	Sequence 41 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01933	PIDISIELNKAKSDLEESKEWIRRSNQKLDSIGNW	35	Sequence 42 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01934	IDISIELNKAKSDLEESKEWIRRSNQKLDSIGNWH	35	Sequence 43 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01935	DISIELNKAKSDLEESKEWIRRSNQKLDSIGNWHQ	35	Sequence 44 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01936	ISIELNKAKSDLEESKEWIRRSNQKLDSIGNWHQS	35	Sequence 45 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01937	SIELNKAKSDLEESKEWIRRSNQKLDSIGNWHQSS	35	Sequence 46 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01938	IELNKAKSDLEESKEWIRRSNQKLDSIGNWHQSST	35	Sequence 47 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01939	ELNKAKSDLEESKEWIRRSNQKLDSIGNWHQSSTT	35	Sequence 48 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01940	TAAVALVEAKQARSDIEKLKEAIRDTNKAVQSVQS	35	Sequence 49 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01941	AVALVEAKQARSDIEKLKEAIRDTNKAVQSVQSSI	35	Sequence 50 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01942	LVEAKQARSDIEKLKEAIRDTNKAVQSVQSSIGNL	35	Sequence 51 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01943	VEAKQARSDIEKLKEAIRDTNKAVQSVQSSIGNLI	35	Sequence 52 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01944	EAKQARSDIEKLKEAIRDTNKAVQSVQSSIGNLIV	35	Sequence 53 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01945	AKQARSDIEKLKEAIRDTNKAVQSVQSSIGNLIVA	35	Sequence 54 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01946	KQARSDIEKLKEAIRDTNKAVQSVQSSIGNLIVAI	35	Sequence 55 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01947	QARSDIEKLKEAIRDTNKAVQSVQSSIGNLIVAIK	35	Sequence 56 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01948	ARSDIEKLKEAIRDTNKAVQSVQSSIGNLIVAIKS	35	Sequence 57 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01949	RSDIEKLKEAIRDTNKAVQSVQSSIGNLIVAIKSV	35	Sequence 58 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01950	SDIEKLKEAIRDTNKAVQSVQSSIGNLIVAIKSVQ	35	Sequence 59 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01951	KLKEAIRDTNKAVQSVQSSIGNLIVAIKSVQDYVN	35	Sequence 60 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01952	LKEAIRDTNKAVQSVQSSIGNLIVAIKSVQDYVNK	35	Sequence 61 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01953	AIRDTNKAVQSVQSSIGNLIVAIKSVQDYVNKEIV	35	Sequence 62 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01954	TWQEWERKVDFLEENITALLEEAQIQQEKNMYELQKLNSWDVFGNWF	47	Sequence 63 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01955	WQEWERKVDFLEENITALLEEAQIQQEKNMYELQK	35	Sequence 64 from Patent US 7582301 B1	Synthetic construct	SIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01956	QEWERKVDFLEENITALLEEAQIQQEKNMYELQKL	35	Sequence 65 from Patent US 7582301 B1	Synthetic construct	SIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01957	EWERKVDFLEENITALLEEAQIQQEKNMYELQKLN	35	Sequence 66 from Patent US 7582301 B1	Synthetic construct	SIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01958	WERKVDFLEENITALLEEAQIQQEKNMYELQKLNS	35	Sequence 67 from Patent US 7582301 B1	Synthetic construct	SIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01959	ERKVDFLEENITALLEEAQIQQEKNMYELQKLNSW	35	Sequence 68 from Patent US 7582301 B1	Synthetic construct	SIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01960	RKVDFLEENITALLEEAQIQQEKNMYELQKLNSWD	35	Sequence 69 from Patent US 7582301 B1	Synthetic construct	SIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01961	KVDFLEENITALLEEAQIQQEKNMYELQKLNSWDV	35	Sequence 70 from Patent US 7582301 B1	Synthetic construct	SIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01962	VDFLEENITALLEEAQIQQEKNMYELQKLNSWDVF	35	Sequence 71 from Patent US 7582301 B1	Synthetic construct	SIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01963	DFLEENITALLEEAQIQQEKNMYELQKLNSWDVFG	35	Sequence 72 from Patent US 7582301 B1	Synthetic construct	SIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01964	FLEENITALLEEAQIQQEKNMYELQKLNSWDVFGN	35	Sequence 73 from Patent US 7582301 B1	Synthetic construct	SIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01965	PDAVYLHRIDLGPPISLERLDVGTNLGNAIAKLED	35	Sequence 74 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01966	LERLDVGTNLGNAIAKLEAKELLESSDQILRSMK	34	Sequence 75 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01967	LHRIDLGPPISLERLDVGTNLGNAIAKLEAKELL	34	Sequence 76 from Patent US 7582301 B1	Synthetic construct	MeV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01968	HRIDLGPPISLERLDVGTNLGNAIAKLEAKELLE	34	Sequence 77 from Patent US 7582301 B1	Synthetic construct	MeV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01969	RIDLGPPISLERLDVGTNLGNAIAKLEAKELLES	34	Sequence 78 from Patent US 7582301 B1	Synthetic construct	MeV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01970	IDLGPPISLERLDVGTNLGNAIAKLEAKELLESS	34	Sequence 79 from Patent US 7582301 B1	Synthetic construct	MeV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01971	DLGPPISLERLDVGTNLGNAIAKLEAKELLESSD	34	Sequence 80 from Patent US 7582301 B1	Synthetic construct	MeV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01972	LGPPISLERLDVGTNLGNAIAKLEAKELLESSDQ	34	Sequence 81 from Patent US 7582301 B1	Synthetic construct	MeV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01973	GPPISLERLDVGTNLGNAIAKLEAKELLESSDQI	34	Sequence 82 from Patent US 7582301 B1	Synthetic construct	MeV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01974	PPISLERLDVGTNLGNAIAKLEAKELLESSDQIL	34	Sequence 83 from Patent US 7582301 B1	Synthetic construct	MeV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01975	PISLERLDVGTNLGNAIAKLEAKELLESSDQILR	34	Sequence 84 from Patent US 7582301 B1	Synthetic construct	MeV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01976	SLERLDVGTNLGNAIAKLEAKELLESSDQILRSM	34	Sequence 85 from Patent US 7582301 B1	Synthetic construct	MeV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01977	LERLDVGTNLGNAIAKLEAKELLESSDQILRSMK	34	Sequence 86 from Patent US 7582301 B1	Synthetic construct	MeV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01978	YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNW	35	Sequence 87 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01979	YTSLIHSLIEESQNQQEKNEQELLELDKWASLWN	34	Sequence 88 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01980	YTSLIHSLIEESQNQQEKNEQELLELDKWASLW	33	Sequence 89 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01981	YTSLIHSLIEESQNQQEKNEQELLELDKWASL	32	Sequence 90 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01982	YTSLIHSLIEESQNQQEKNEQELLELDKWAS	31	Sequence 91 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01983	YTSLIHSLIEESQNQQEKNEQELLELDKWA	30	Sequence 92 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01984	YTSLIHSLIEESQNQQEKNEQELLELDKW	29	Sequence 93 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01985	YTSLIHSLIEESQNQQEKNEQELLELDK	28	Sequence 94 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01986	YTSLIHSLIEESQNQQEKNEQELLELD	27	Sequence 95 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01987	YTSLIHSLIEESQNQQEKNEQELLEL	26	Sequence 96 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01988	YTSLIHSLIEESQNQQEKNEQELLE	25	Sequence 97 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01989	YTSLIHSLIEESQNQQEKNEQELL	24	Sequence 98 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01990	YTSLIHSLIEESQNQQEKNEQEL	23	Sequence 99 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01991	YTSLIHSLIEESQNQQEKNEQE	22	Sequence 100 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01992	YTSLIHSLIEESQNQQEKNEQ	21	Sequence 101 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01993	YTSLIHSLIEESQNQQEKNE	20	Sequence 102 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01994	YTSLIHSLIEESQNQQEKN	19	Sequence 103 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01995	YTSLIHSLIEESQNQQEK	18	Sequence 104 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01996	YTSLIHSLIEESQNQQE	17	Sequence 105 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01997	YTSLIHSLIEESQNQQ	16	Sequence 106 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01998	YTSLIHSLIEESQNQ	15	Sequence 107 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP01999	YTSLIHSLIEESQN	14	Sequence 108 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02000	YTSLIHSLIEESQ	13	Sequence 109 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02001	YTSLIHSLIEES	12	Sequence 110 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02002	YTSLIHSLIEE	11	Sequence 111 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02003	YTSLIHSLIE	10	Sequence 112 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02004	YTSLIHSLI	9	Sequence 113 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02005	YTSLIHSL	8	Sequence 114 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02006	YTSLIHS	7	Sequence 115 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02007	YTSLIH	6	Sequence 116 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02008	TSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	35	Sequence 117 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02009	SLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	34	Sequence 118 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02010	LIHSLIEESQNQQEKNEQELLELDKWASLWNWF	33	Sequence 119 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02011	IHSLIEESQNQQEKNEQELLELDKWASLWNWF	32	Sequence 120 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02012	HSLIEESQNQQEKNEQELLELDKWASLWNWF	31	Sequence 121 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02013	SLIEESQNQQEKNEQELLELDKWASLWNWF	30	Sequence 122 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02014	LIEESQNQQEKNEQELLELDKWASLWNWF	29	Sequence 123 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02015	IEESQNQQEKNEQELLELDKWASLWNWF	28	Sequence 124 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02016	EESQNQQEKNEQELLELDKWASLWNWF	27	Sequence 125 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02017	ESQNQQEKNEQELLELDKWASLWNWF	26	Sequence 126 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02018	SQNQQEKNEQELLELDKWASLWNWF	25	Sequence 127 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02019	QNQQEKNEQELLELDKWASLWNWF	24	Sequence 128 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02020	NQQEKNEQELLELDKWASLWNWF	23	Sequence 129 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02021	QQEKNEQELLELDKWASLWNWF	22	Sequence 130 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02022	QEKNEQELLELDKWASLWNWF	21	Sequence 131 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02023	EKNEQELLELDKWASLWNWF	20	Sequence 132 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02024	KNEQELLELDKWASLWNWF	19	Sequence 133 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02025	NEQELLELDKWASLWNWF	18	Sequence 134 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02026	EQELLELDKWASLWNWF	17	Sequence 135 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02027	QELLELDKWASLWNWF	16	Sequence 136 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02028	ELLELDKWASLWNWF	15	Sequence 137 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02029	LLELDKWASLWNWF	14	Sequence 138 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02030	LELDKWASLWNWF	13	Sequence 139 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02031	ELDKWASLWNWF	12	Sequence 140 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02032	LDKWASLWNWF	11	Sequence 141 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02033	DKWASLWNWF	10	Sequence 142 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02034	KWASLWNWF	9	Sequence 143 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02035	WASLWNWF	8	Sequence 144 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02036	ASLWNWF	7	Sequence 145 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02037	SLWNWF	6	Sequence 146 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02038	NNLLRAIEAQQHLLQLTVWQIKQLQARILAVERYLKD	37	Sequence 147 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02039	NNLLRAIEAQQHLLQLTVWQIKQLQARILAVERYLK	36	Sequence 148 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02040	NNLLRAIEAQQHLLQLTVWQIKQLQARILAVERYL	35	Sequence 149 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02041	NNLLRAIEAQQHLLQLTVWQIKQLQARILAVERY	34	Sequence 150 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02042	NNLLRAIEAQQHLLQLTVWQIKQLQARILAVER	33	Sequence 151 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02043	NNLLRAIEAQQHLLQLTVWQIKQLQARILAVE	32	Sequence 152 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02044	NNLLRAIEAQQHLLQLTVWQIKQLQARILAV	31	Sequence 153 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02045	NNLLRAIEAQQHLLQLTVWQIKQLQARILA	30	Sequence 154 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02046	NNLLRAIEAQQHLLQLTVWQIKQLQARIL	29	Sequence 155 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02047	NNLLRAIEAQQHLLQLTVWQIKQLQARI	28	Sequence 156 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02048	NNLLRAIEAQQHLLQLTVWQIKQLQAR	27	Sequence 157 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02049	NNLLRAIEAQQHLLQLTVWQIKQLQA	26	Sequence 158 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02050	NNLLRAIEAQQHLLQLTVWQIKQLQ	25	Sequence 159 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02051	NNLLRAIEAQQHLLQLTVWQIKQL	24	Sequence 160 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02052	NNLLRAIEAQQHLLQLTVWQIKQ	23	Sequence 161 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02053	NNLLRAIEAQQHLLQLTVWQIK	22	Sequence 162 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02054	NNLLRAIEAQQHLLQLTVWQI	21	Sequence 163 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02055	NNLLRAIEAQQHLLQLTVWQ	20	Sequence 164 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02056	NNLLRAIEAQQHLLQLTVW	19	Sequence 165 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02057	NNLLRAIEAQQHLLQLTV	18	Sequence 166 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02058	NNLLRAIEAQQHLLQLT	17	Sequence 167 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02059	NNLLRAIEAQQHLLQL	16	Sequence 168 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02060	NNLLRAIEAQQHLLQ	15	Sequence 169 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02061	NNLLRAIEAQQHLL	14	Sequence 170 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02062	NNLLRAIEAQQHL	13	Sequence 171 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02063	NNLLRAIEAQQH	12	Sequence 172 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02064	NNLLRAIEAQQ	11	Sequence 173 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02065	NNLLRAIEAQ	10	Sequence 174 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02066	NNLLRAIEA	9	Sequence 175 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02067	NNLLRAIE	8	Sequence 176 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02068	NNLLRAI	7	Sequence 177 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02069	NNLLRA	6	Sequence 178 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02070	NLLRAIEAQQHLLQLTVWQIKQLQARILAVERYLKDQ	37	Sequence 179 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02071	LLRAIEAQQHLLQLTVWQIKQLQARILAVERYLKDQ	36	Sequence 180 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02072	LRAIEAQQHLLQLTVWQIKQLQARILAVERYLKDQ	35	Sequence 181 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02073	RAIEAQQHLLQLTVWQIKQLQARILAVERYLKDQ	34	Sequence 182 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02074	AIEAQQHLLQLTVWQIKQLQARILAVERYLKDQ	33	Sequence 183 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02075	IEAQQHLLQLTVWQIKQLQARILAVERYLKDQ	32	Sequence 184 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02076	EAQQHLLQLTVWQIKQLQARILAVERYLKDQ	31	Sequence 185 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02077	AQQHLLQLTVWQIKQLQARILAVERYLKDQ	30	Sequence 186 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02078	QQHLLQLTVWQIKQLQARILAVERYLKDQ	29	Sequence 187 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02079	QHLLQLTVWQIKQLQARILAVERYLKDQ	28	Sequence 188 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02080	HLLQLTVWQIKQLQARILAVERYLKDQ	27	Sequence 189 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02081	LLQLTVWQIKQLQARILAVERYLKDQ	26	Sequence 190 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02082	LQLTVWQIKQLQARILAVERYLKDQ	25	Sequence 191 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02083	QLTVWQIKQLQARILAVERYLKDQ	24	Sequence 192 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02084	LTVWQIKQLQARILAVERYLKDQ	23	Sequence 193 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02085	TVWQIKQLQARILAVERYLKDQ	22	Sequence 194 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02086	VWQIKQLQARILAVERYLKDQ	21	Sequence 195 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02087	WQIKQLQARILAVERYLKDQ	20	Sequence 196 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02088	QIKQLQARILAVERYLKDQ	19	Sequence 197 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02089	IKQLQARILAVERYLKDQ	18	Sequence 198 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02090	KQLQARILAVERYLKDQ	17	Sequence 199 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02091	QLQARILAVERYLKDQ	16	Sequence 200 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02092	LQARILAVERYLKDQ	15	Sequence 201 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02093	QARILAVERYLKDQ	14	Sequence 202 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02094	ARILAVERYLKDQ	13	Sequence 203 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02095	RILAVERYLKDQ	12	Sequence 204 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02096	ILAVERYLKDQ	11	Sequence 205 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02097	LAVERYLKDQ	10	Sequence 206 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02098	AVERYLKDQ	9	Sequence 207 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02099	VERYLKDQ	8	Sequence 208 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02100	ERYLKDQ	7	Sequence 209 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02101	RYLKDQ	6	Sequence 210 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP107."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02102	LEANISQSLEQAQIQQEKNMYELQKLNSWDVFTNW	35	Sequence 211 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02103	LEANISQSLEQAQIQQEKNMYELQKLNSWDVFTN	34	Sequence 212 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02104	LEANISQSLEQAQIQQEKNMYELQKLNSWDVFT	33	Sequence 213 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02105	LEANISQSLEQAQIQQEKNMYELQKLNSWDVF	32	Sequence 214 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02106	LEANISQSLEQAQIQQEKNMYELQKLNSWDV	31	Sequence 215 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02107	LEANISQSLEQAQIQQEKNMYELQKLNSWD	30	Sequence 216 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02108	LEANISQSLEQAQIQQEKNMYELQKLNSW	29	Sequence 217 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02109	LEANISQSLEQAQIQQEKNMYELQKLNS	28	Sequence 218 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02110	LEANISQSLEQAQIQQEKNMYELQKLN	27	Sequence 219 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02111	LEANISQSLEQAQIQQEKNMYELQKL	26	Sequence 220 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02112	LEANISQSLEQAQIQQEKNMYELQK	25	Sequence 221 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02113	LEANISQSLEQAQIQQEKNMYELQ	24	Sequence 222 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02114	LEANISQSLEQAQIQQEKNMYEL	23	Sequence 223 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02115	LEANISQSLEQAQIQQEKNMYE	22	Sequence 224 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02116	LEANISQSLEQAQIQQEKNMY	21	Sequence 225 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02117	LEANISQSLEQAQIQQEKNM	20	Sequence 226 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02118	LEANISQSLEQAQIQQEKN	19	Sequence 227 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02119	LEANISQSLEQAQIQQEK	18	Sequence 228 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02120	LEANISQSLEQAQIQQE	17	Sequence 229 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02121	LEANISQSLEQAQIQQ	16	Sequence 230 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02122	LEANISQSLEQAQIQ	15	Sequence 231 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02123	LEANISQSLEQAQI	14	Sequence 232 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02124	LEANISQSLEQAQ	13	Sequence 233 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02125	LEANISQSLEQA	12	Sequence 234 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02126	LEANISQSLEQ	11	Sequence 235 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02127	LEANISQSLE	10	Sequence 236 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02128	LEANISQSL	9	Sequence 237 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02129	LEANISQS	8	Sequence 238 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02130	LEANISQ	7	Sequence 239 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02131	LEANIS	6	Sequence 240 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02132	EANISQSLEQAQIQQEKNMYELQKLNSWDVFTNWL	35	Sequence 241 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02133	ANISQSLEQAQIQQEKNMYELQKLNSWDVFTNWL	34	Sequence 242 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02134	NISQSLEQAQIQQEKNMYELQKLNSWDVFTNWL	33	Sequence 243 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02135	ISQSLEQAQIQQEKNMYELQKLNSWDVFTNWL	32	Sequence 244 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02136	SQSLEQAQIQQEKNMYELQKLNSWDVFTNWL	31	Sequence 245 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02137	QSLEQAQIQQEKNMYELQKLNSWDVFTNWL	30	Sequence 246 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02138	SLEQAQIQQEKNMYELQKLNSWDVFTNWL	29	Sequence 247 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02139	LEQAQIQQEKNMYELQKLNSWDVFTNWL	28	Sequence 248 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02140	EQAQIQQEKNMYELQKLNSWDVFTNWL	27	Sequence 249 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02141	QAQIQQEKNMYELQKLNSWDVFTNWL	26	Sequence 250 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02142	AQIQQEKNMYELQKLNSWDVFTNWL	25	Sequence 251 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02143	QIQQEKNMYELQKLNSWDVFTNWL	24	Sequence 252 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02144	IQQEKNMYELQKLNSWDVFTNWL	23	Sequence 253 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02145	QQEKNMYELQKLNSWDVFTNWL	22	Sequence 254 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02146	QEKNMYELQKLNSWDVFTNWL	21	Sequence 255 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02147	EKNMYELQKLNSWDVFTNWL	20	Sequence 256 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02148	KNMYELQKLNSWDVFTNWL	19	Sequence 257 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02149	NMYELQKLNSWDVFTNWL	18	Sequence 258 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02150	MYELQKLNSWDVFTNWL	17	Sequence 259 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02151	YELQKLNSWDVFTNWL	16	Sequence 260 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02152	ELQKLNSWDVFTNWL	15	Sequence 261 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02153	LQKLNSWDVFTNWL	14	Sequence 262 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02154	QKLNSWDVFTNWL	13	Sequence 263 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02155	KLNSWDVFTNWL	12	Sequence 264 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02156	LNSWDVFTNWL	11	Sequence 265 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02157	NSWDVFTNWL	10	Sequence 266 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02158	SWDVFTNWL	9	Sequence 267 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02159	WDVFTNWL	8	Sequence 268 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02160	DVFTNWL	7	Sequence 269 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02161	VFTNWL	6	Sequence 270 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	"The peptide was potent inhibitors of HIV-1 infection and HIV induced cell-cell fusion, which derived from DP178."	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02162	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQS	47	Sequence 271 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02163	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQ	46	Sequence 272 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02164	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLM	45	Sequence 273 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02165	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLL	44	Sequence 274 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02166	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQL	43	Sequence 275 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02167	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQ	42	Sequence 276 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02168	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTEL	41	Sequence 277 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02169	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTE	40	Sequence 278 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02170	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVT	39	Sequence 279 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02171	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAV	38	Sequence 280 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02172	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNA	37	Sequence 281 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02173	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKN	36	Sequence 282 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02174	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYK	35	Sequence 283 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02175	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKY	34	Sequence 284 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02176	YTSVITIELSNIKENKCNGTDAKVKLIKQELDK	33	Sequence 285 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02177	YTSVITIELSNIKENKCNGTDAKVKLIKQELD	32	Sequence 286 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02178	YTSVITIELSNIKENKCNGTDAKVKLIKQEL	31	Sequence 287 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02179	YTSVITIELSNIKENKCNGTDAKVKLIKQE	30	Sequence 288 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02180	YTSVITIELSNIKENKCNGTDAKVKLIKQ	29	Sequence 289 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02181	YTSVITIELSNIKENKCNGTDAKVKLIK	28	Sequence 290 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02182	YTSVITIELSNIKENKCNGTDAKVKLI	27	Sequence 291 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02183	YTSVITIELSNIKENKCNGTDAKVKL	26	Sequence 292 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02184	YTSVITIELSNIKENKCNGTDAKVK	25	Sequence 293 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02185	YTSVITIELSNIKENKCNGTDAKV	24	Sequence 294 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02186	YTSVITIELSNIKENKCNGTDAK	23	Sequence 295 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02187	YTSVITIELSNIKENKCNGTDA	22	Sequence 296 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02188	YTSVITIELSNIKENKCNGTD	21	Sequence 297 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02189	YTSVITIELSNIKENKCNGT	20	Sequence 298 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02190	YTSVITIELSNIKENKCNG	19	Sequence 299 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02191	YTSVITIELSNIKENKCN	18	Sequence 300 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02192	YTSVITIELSNIKENKC	17	Sequence 301 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02193	YTSVITIELSNIKENK	16	Sequence 302 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02194	YTSVITIELSNIKEN	15	Sequence 303 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02195	YTSVITIELSNIKE	14	Sequence 304 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02196	YTSVITIELSNIK	13	Sequence 305 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02197	YTSVITIELSNI	12	Sequence 306 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02198	YTSVITIELSN	11	Sequence 307 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02199	YTSVITIELS	10	Sequence 308 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02200	YTSVITIEL	9	Sequence 309 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02201	YTSVITIE	8	Sequence 310 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02202	YTSVITI	7	Sequence 311 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02203	YTSVIT	6	Sequence 312 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02204	TSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	47	Sequence 313 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02205	SVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	46	Sequence 314 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02206	VITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	45	Sequence 315 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02207	ITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	44	Sequence 316 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02208	TIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	43	Sequence 317 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02209	IELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	42	Sequence 318 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02210	ELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	41	Sequence 319 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02211	LSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	40	Sequence 320 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02212	SNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	39	Sequence 321 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02213	NIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	38	Sequence 322 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02214	IKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	37	Sequence 323 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02215	KENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	36	Sequence 324 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02216	NKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	34	Sequence 325 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02217	KCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	33	Sequence 326 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02218	CNGTDAKVKLIKQELDKYKNAVTELQLLMQST	32	Sequence 327 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02219	NGTDAKVKLIKQELDKYKNAVTELQLLMQST	31	Sequence 328 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02220	GTDAKVKLIKQELDKYKNAVTELQLLMQST	30	Sequence 329 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02221	TDAKVKLIKQELDKYKNAVTELQLLMQST	29	Sequence 330 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02222	DAKVKLIKQELDKYKNAVTELQLLMQST	28	Sequence 331 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02223	AKVKLIKQELDKYKNAVTELQLLMQST	27	Sequence 332 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02224	KVKLIKQELDKYKNAVTELQLLMQST	26	Sequence 333 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02225	VKLIKQELDKYKNAVTELQLLMQST	25	Sequence 334 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02226	KLIKQELDKYKNAVTELQLLMQST	24	Sequence 335 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02227	LIKQELDKYKNAVTELQLLMQST	23	Sequence 336 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02228	IKQELDKYKNAVTELQLLMQST	22	Sequence 337 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02229	KQELDKYKNAVTELQLLMQST	21	Sequence 338 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02230	QELDKYKNAVTELQLLMQST	20	Sequence 339 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02231	ELDKYKNAVTELQLLMQST	19	Sequence 340 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02232	LDKYKNAVTELQLLMQST	18	Sequence 341 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02233	DKYKNAVTELQLLMQST	17	Sequence 342 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02234	KYKNAVTELQLLMQST	16	Sequence 343 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02235	YKNAVTELQLLMQST	15	Sequence 344 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02236	KNAVTELQLLMQST	14	Sequence 345 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02237	NAVTELQLLMQST	13	Sequence 346 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02238	AVTELQLLMQST	12	Sequence 347 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02239	VTELQLLMQST	11	Sequence 348 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02240	TELQLLMQST	10	Sequence 349 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02241	ELQLLMQST	9	Sequence 350 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02242	LQLLMQST	8	Sequence 351 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02243	QLLMQST	7	Sequence 352 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02244	LLMQST	6	Sequence 353 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02245	FYDPLVFPSDEFDASISQVNEKINQSLAFIRKSDELL	37	Sequence 354 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02246	FYDPLVFPSDEFDASISQVNEKINQSLAFIRKSDEL	36	Sequence 355 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02247	FYDPLVFPSDEFDASISQVNEKINQSLAFIRKSDE	35	Sequence 356 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02248	FYDPLVFPSDEFDASISQVNEKINQSLAFIRKSD	34	Sequence 357 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02249	FYDPLVFPSDEFDASISQVNEKINQSLAFIRKS	33	Sequence 358 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02250	FYDPLVFPSDEFDASISQVNEKINQSLAFIRK	32	Sequence 359 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02251	FYDPLVFPSDEFDASISQVNEKINQSLAFIR	31	Sequence 360 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02252	FYDPLVFPSDEFDASISQVNEKINQSLAFI	30	Sequence 361 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02253	FYDPLVFPSDEFDASISQVNEKINQSLAF	29	Sequence 362 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02254	FYDPLVFPSDEFDASISQVNEKINQSLA	28	Sequence 363 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02255	FYDPLVFPSDEFDASISQVNEKINQSL	27	Sequence 364 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02256	FYDPLVFPSDEFDASISQVNEKINQS	26	Sequence 365 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02257	FYDPLVFPSDEFDASISQVNEKINQ	25	Sequence 366 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02258	FYDPLVFPSDEFDASISQVNEKIN	24	Sequence 367 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02259	FYDPLVFPSDEFDASISQVNEKI	23	Sequence 368 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02260	FYDPLVFPSDEFDASISQVNEK	22	Sequence 369 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02261	FYDPLVFPSDEFDASISQVNE	21	Sequence 370 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02262	FYDPLVFPSDEFDASISQVN	20	Sequence 371 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02263	FYDPLVFPSDEFDASISQV	19	Sequence 372 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02264	FYDPLVFPSDEFDASISQ	18	Sequence 373 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02265	FYDPLVFPSDEFDASIS	17	Sequence 374 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02266	FYDPLVFPSDEFDASI	16	Sequence 375 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02267	FYDPLVFPSDEFDAS	15	Sequence 376 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02268	FYDPLVFPSDEFDA	14	Sequence 377 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02269	FYDPLVFPSDEFD	13	Sequence 378 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02270	FYDPLVFPSDEF	12	Sequence 379 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02271	FYDPLVFPSDE	11	Sequence 380 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02272	FYDPLVFPSD	10	Sequence 381 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02273	FYDPLVFPS	9	Sequence 382 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02274	FYDPLVFP	8	Sequence 383 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02275	FYDPLVF	7	Sequence 384 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02276	FYDPLV	6	Sequence 385 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02277	YDPLVFPSDEFDASISQVNEKINQSLAFIRKSDELL	36	Sequence 386 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02278	DPLVFPSDEFDASISQVNEKINQSLAFIRKSDELL	35	Sequence 387 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02279	PLVFPSDEFDASISQVNEKINQSLAFIRKSDELL	34	Sequence 388 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02280	LVFPSDEFDASISQVNEKINQSLAFIRKSDELL	33	Sequence 389 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02281	VFPSDEFDASISQVNEKINQSLAFIRKSDELL	32	Sequence 390 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02282	FPSDEFDASISQVNEKINQSLAFIRKSDELL	31	Sequence 391 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02283	PSDEFDASISQVNEKINQSLAFIRKSDELL	30	Sequence 392 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02284	SDEFDASISQVNEKINQSLAFIRKSDELL	29	Sequence 393 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02285	DEFDASISQVNEKINQSLAFIRKSDELL	28	Sequence 394 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02286	EFDASISQVNEKINQSLAFIRKSDELL	27	Sequence 395 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02287	FDASISQVNEKINQSLAFIRKSDELL	26	Sequence 396 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02288	DASISQVNEKINQSLAFIRKSDELL	25	Sequence 397 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02289	ASISQVNEKINQSLAFIRKSDELL	24	Sequence 398 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02290	SISQVNEKINQSLAFIRKSDELL	23	Sequence 399 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02291	ISQVNEKINQSLAFIRKSDELL	22	Sequence 400 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02292	SQVNEKINQSLAFIRKSDELL	21	Sequence 401 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02293	QVNEKINQSLAFIRKSDELL	20	Sequence 402 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02294	VNEKINQSLAFIRKSDELL	19	Sequence 403 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02295	NEKINQSLAFIRKSDELL	18	Sequence 404 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02296	EKINQSLAFIRKSDELL	17	Sequence 405 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02297	KINQSLAFIRKSDELL	16	Sequence 406 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02298	INQSLAFIRKSDELL	15	Sequence 407 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02299	NQSLAFIRKSDELL	14	Sequence 408 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02300	QSLAFIRKSDELL	13	Sequence 409 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02301	SLAFIRKSDELL	12	Sequence 410 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02302	LAFIRKSDELL	11	Sequence 411 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02303	AFIRKSDELL	10	Sequence 412 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02304	FIRKSDELL	9	Sequence 413 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02305	IRKSDELL	8	Sequence 414 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02306	RKSDELL	7	Sequence 415 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02307	KSDELL	6	Sequence 416 from Patent US 7582301 B1	Synthetic construct	RSV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02308	ITLNNSVALDPIDISIELNKAKSDLEESKEWIRRS	35	Sequence 417 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02309	ITLNNSVALDPIDISIELNKAKSDLEESKEWIRR	34	Sequence 418 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02310	ITLNNSVALDPIDISIELNKAKSDLEESKEWIR	33	Sequence 419 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02311	ITLNNSVALDPIDISIELNKAKSDLEESKEWI	32	Sequence 420 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02312	ITLNNSVALDPIDISIELNKAKSDLEESKEW	31	Sequence 421 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02313	ITLNNSVALDPIDISIELNKAKSDLEESKE	30	Sequence 422 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02314	ITLNNSVALDPIDISIELNKAKSDLEESK	29	Sequence 423 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02315	ITLNNSVALDPIDISIELNKAKSDLEES	28	Sequence 424 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02316	ITLNNSVALDPIDISIELNKAKSDLEE	27	Sequence 425 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02317	ITLNNSVALDPIDISIELNKAKSDLE	26	Sequence 426 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02318	ITLNNSVALDPIDISIELNKAKSDL	25	Sequence 427 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02319	ITLNNSVALDPIDISIELNKAKSD	24	Sequence 428 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02320	ITLNNSVALDPIDISIELNKAKS	23	Sequence 429 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02321	ITLNNSVALDPIDISIELNKAK	22	Sequence 430 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02322	ITLNNSVALDPIDISIELNKA	21	Sequence 431 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02323	ITLNNSVALDPIDISIELNK	20	Sequence 432 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02324	ITLNNSVALDPIDISIELN	19	Sequence 433 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02325	ITLNNSVALDPIDISIEL	18	Sequence 434 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02326	ITLNNSVALDPIDISIE	17	Sequence 435 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02327	ITLNNSVALDPIDISI	16	Sequence 436 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02328	ITLNNSVALDPIDIS	15	Sequence 437 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02329	ITLNNSVALDPIDI	14	Sequence 438 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02330	ITLNNSVALDPID	13	Sequence 439 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02331	ITLNNSVALDPI	12	Sequence 440 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02332	ITLNNSVALDP	11	Sequence 441 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02333	ITLNNSVALD	10	Sequence 442 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02334	ITLNNSVAL	9	Sequence 443 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02335	ITLNNSVA	8	Sequence 444 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02336	ITLNNSV	7	Sequence 445 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02337	ITLNNS	6	Sequence 446 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02338	TLNNSVALDPIDISIELNKAKSDLEESKEWIRRS	34	Sequence 447 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02339	LNNSVALDPIDISIELNKAKSDLEESKEWIRRS	33	Sequence 448 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02340	NNSVALDPIDISIELNKAKSDLEESKEWIRRS	32	Sequence 449 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02341	NSVALDPIDISIELNKAKSDLEESKEWIRRS	31	Sequence 450 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02342	SVALDPIDISIELNKAKSDLEESKEWIRRS	30	Sequence 451 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02343	VALDPIDISIELNKAKSDLEESKEWIRRS	29	Sequence 452 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02344	ALDPIDISIELNKAKSDLEESKEWIRRS	28	Sequence 453 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02345	LDPIDISIELNKAKSDLEESKEWIRRS	27	Sequence 454 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02346	DPIDISIELNKAKSDLEESKEWIRRS	26	Sequence 455 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02347	PIDISIELNKAKSDLEESKEWIRRS	25	Sequence 456 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02348	IDISIELNKAKSDLEESKEWIRRS	24	Sequence 457 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02349	DISIELNKAKSDLEESKEWIRRS	23	Sequence 458 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02350	ISIELNKAKSDLEESKEWIRRS	22	Sequence 459 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02351	SIELNKAKSDLEESKEWIRRS	21	Sequence 460 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02352	IELNKAKSDLEESKEWIRRS	20	Sequence 461 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02353	ELNKAKSDLEESKEWIRRS	19	Sequence 462 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02354	LNKAKSDLEESKEWIRRS	18	Sequence 463 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02355	NKAKSDLEESKEWIRRS	17	Sequence 464 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02356	KAKSDLEESKEWIRRS	16	Sequence 465 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02357	AKSDLEESKEWIRRS	15	Sequence 466 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02358	KSDLEESKEWIRRS	14	Sequence 467 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02359	SDLEESKEWIRRS	13	Sequence 468 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02360	DLEESKEWIRRS	12	Sequence 469 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02361	LEESKEWIRRS	11	Sequence 470 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02362	EESKEWIRRS	10	Sequence 471 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02363	ESKEWIRRS	9	Sequence 472 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02364	SKEWIRRS	8	Sequence 473 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02365	KEWIRRS	7	Sequence 474 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02366	EWIRRS	6	Sequence 475 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02367	ALGVATSAQITAAVALVEAKQARSDIEKLKEAIR	34	Sequence 476 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02368	ALGVATSAQITAAVALVEAKQARSDIEKLKEAI	33	Sequence 477 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02369	ALGVATSAQITAAVALVEAKQARSDIEKLKEA	32	Sequence 478 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02370	ALGVATSAQITAAVALVEAKQARSDIEKLKE	31	Sequence 479 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02371	ALGVATSAQITAAVALVEAKQARSDIEKLK	30	Sequence 480 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02372	ALGVATSAQITAAVALVEAKQARSDIEKL	29	Sequence 481 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02373	ALGVATSAQITAAVALVEAKQARSDIEK	28	Sequence 482 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02374	ALGVATSAQITAAVALVEAKQARSDIE	27	Sequence 483 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02375	ALGVATSAQITAAVALVEAKQARSDI	26	Sequence 484 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02376	ALGVATSAQITAAVALVEAKQARSD	25	Sequence 485 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02377	ALGVATSAQITAAVALVEAKQARS	24	Sequence 486 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02378	ALGVATSAQITAAVALVEAKQAR	23	Sequence 487 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02379	ALGVATSAQITAAVALVEAKQA	22	Sequence 488 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02380	ALGVATSAQITAAVALVEAKQ	21	Sequence 489 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02381	ALGVATSAQITAAVALVEAK	20	Sequence 490 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02382	ALGVATSAQITAAVALVEA	19	Sequence 491 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02383	ALGVATSAQITAAVALVE	18	Sequence 492 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02384	ALGVATSAQITAAVALV	17	Sequence 493 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02385	ALGVATSAQITAAVAL	16	Sequence 494 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02386	ALGVATSAQITAAVA	15	Sequence 495 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02387	ALGVATSAQITAAV	14	Sequence 496 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02388	ALGVATSAQITAA	13	Sequence 497 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02389	ALGVATSAQITA	12	Sequence 498 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02390	ALGVATSAQIT	11	Sequence 499 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02391	ALGVATSAQI	10	Sequence 500 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02392	ALGVATSAQ	9	Sequence 501 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02393	ALGVATSA	8	Sequence 502 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02394	ALGVATS	7	Sequence 503 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02395	ALGVAT	6	Sequence 504 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02396	LGVATSAQITAAVALVEAKQARSDIEKLKEAIRD	34	Sequence 505 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02397	GVATSAQITAAVALVEAKQARSDIEKLKEAIRD	33	Sequence 506 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02398	VATSAQITAAVALVEAKQARSDIEKLKEAIRD	32	Sequence 507 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02399	ATSAQITAAVALVEAKQARSDIEKLKEAIRD	31	Sequence 508 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02400	TSAQITAAVALVEAKQARSDIEKLKEAIRD	30	Sequence 509 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02401	SAQITAAVALVEAKQARSDIEKLKEAIRD	29	Sequence 510 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02402	AQITAAVALVEAKQARSDIEKLKEAIRD	28	Sequence 511 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02403	QITAAVALVEAKQARSDIEKLKEAIRD	27	Sequence 512 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02404	ITAAVALVEAKQARSDIEKLKEAIRD	26	Sequence 513 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02405	TAAVALVEAKQARSDIEKLKEAIRD	25	Sequence 514 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02406	AAVALVEAKQARSDIEKLKEAIRD	24	Sequence 515 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02407	AVALVEAKQARSDIEKLKEAIRD	23	Sequence 516 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02408	VALVEAKQARSDIEKLKEAIRD	22	Sequence 517 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02409	ALVEAKQARSDIEKLKEAIRD	21	Sequence 518 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02410	LVEAKQARSDIEKLKEAIRD	20	Sequence 519 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02411	VEAKQARSDIEKLKEAIRD	19	Sequence 520 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02412	EAKQARSDIEKLKEAIRD	18	Sequence 521 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02413	AKQARSDIEKLKEAIRD	17	Sequence 522 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02414	KQARSDIEKLKEAIRD	16	Sequence 523 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02415	QARSDIEKLKEAIRD	15	Sequence 524 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02416	ARSDIEKLKEAIRD	14	Sequence 525 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02417	RSDIEKLKEAIRD	13	Sequence 526 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02418	SDIEKLKEAIRD	12	Sequence 527 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02419	DIEKLKEAIRD	11	Sequence 528 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02420	IEKLKEAIRD	10	Sequence 529 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02421	EKLKEAIRD	9	Sequence 530 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02422	KLKEAIRD	8	Sequence 531 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02423	LKEAIRD	7	Sequence 532 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02424	KEAIRD	6	Sequence 533 from Patent US 7582301 B1	Synthetic construct	HPV 3	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02425	YTGLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 534 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02426	YTNLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 535 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02427	YTSIIHSLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 536 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02428	YTSLIYSLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 537 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02429	YTSLIHRLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 538 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02430	YTSLIHNLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 539 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02431	YTSLIHTLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 540 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02432	YTSLIHSLLEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 541 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02433	SNLLRAIEAQQHLLQLTVWQIKQLQARILAVERYLKDQ	38	Sequence 542 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02434	NNLLRAIDAQQHLLQLTVWQIKQLQARILAVERYLKDQ	38	Sequence 543 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02435	NNLLRAIQAQQHLLQLTVWQIKQLQARILAVERYLKDQ	38	Sequence 544 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02436	NNLLRAIEAQQHMLQLTVWQIKQLQARILAVERYLKDQ	38	Sequence 545 from Patent US 7582301 B1	Synthetic construct	HIV	Granted Patent	US 7582301 B1	2009-09-01	CA 2372338 A1##WO 2000/069902 A1##AU 2000/050271 A##EP 1179012 A1##BR 0010757 A##CN 1351611 A##EP 1179012 B1##AT 226593 T##DE 60000665 D1##EP 1264840 A1##JP 2002544287 A##ES 2185595 T3##AU 761591 B2##	Long-lasting antiviral fusion inhibitor peptide conjugates comprising albumin and human immunodeficiency virus (HIV) peptides	No comments found in patent	"Peptides exhibiting anti-viral and anti-fusogenic activity are modified to provide greater stability and improved half-life in vivo. The selected peptides include fusion inhibitors DP178 and DP107 and related peptides and analogs thereof. The modified peptides are capable of forming covalent bonds with one or more blood components, preferably a mobile blood component."
DRAVP02437	SLEQIWNNMTWEEWDREINNYTELIHELIEESQNQQEKNEQELL	44	Sequence 1 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection.(IC50=0.93 nM against HIV-1 and TC50=14300 nM against PBMC)"	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02438	WEEWDREINNYTKLIHELIEESQNQQEKNEQELL	34	Sequence 2 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection.(IC50=1.41 nM against HIV-1 and TC50=15900 nM against PBMC)"	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02439	WQEWEQKITALLEQAQIQQEKNEYELQKLDKWASLWEWF	39	Sequence 3 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection."	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02440	YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 4 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection."	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02441	WMEWDREINNYTSLIHSLIEESQNQQEKNEQELL	34	Sequence 5 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection."	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02442	WQEWERKVDFLEENITALLEEAQIQQEKNMYELQ	34	Sequence 6 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection."	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02443	WEEWDREINNYTKLIHELIEESQNQQEENEQELL	34	Sequence 7 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection."	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02444	SLEQIWNNMTWEEWDREINNYTXLIHELIEESQNQQEKNEQELL	44	Sequence 8 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The 'X' at position 23 represents a Lysine residue derivatized with a maleimide moiety.The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection."	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02445	SLEQIWNNMTWEEWDREINNYTELIHELIEESQNQQEKNEQELLX	45	Sequence 9 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The 'X' at position 45 represents a Lysine residue derivatized with a maleimide moiety.The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection."	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02446	WEEWDREINNYTXLIHELIEESQNQQEKNEWELL	34	Sequence 10 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The 'X' at position 13 represents a Lysine residue derivatized with a maleimide moiety.The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection.(IC50=3.94 nM against HIV-1 and TC50>25000 nM against PBMC)"	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02447	WEEWDREINNYTELIHELIEESQNQQEKNEQELLX	35	Sequence 11 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The 'X' at position 35 represents a Lysine residue derivatized with a maleimide moiety.The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection.(IC50=9.09 nM against HIV-1 and TC50>25000 nM against PBMC)"	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02448	WQEWEQKITALLXQAQIQQEKNEYELQKLDKWASLWEWF	39	Sequence 12 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The 'X' at position 13 represents a Lysine residue derivatized with a maleimide moiety.The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection.(IC50=7.78 nM against HIV-1 and TC50>25000 nM against PBMC)"	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02449	WQEWEQKITALIEQAQIQQEKNEYELQKLDKWASLWEWFX	40	Sequence 13 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The 'X' at position 40 represents a Lysine residue derivatized with a maleimide moiety.The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection.(IC50=15.7 nM against HIV-1 and TC50>25000 nM against PBMC)"	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02450	WEEWDREINNYTXLIHELIEESQNQQEENEQELL	34	Sequence 14 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The 'X' at position 13 represents a Lysine residue derivatized with a maleimide moiety.The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection."	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02451	WEEWDREINNYTKLIHELIEESQNQQEENEQELLX	35	Sequence 15 from Patent US 7575750 B2	Synthetic construct	"HIV, SIV"	Granted Patent	US 7575750 B2	2009-08-18	WO 2004/029201 A2##CA 2500248 A1##AU 2003/275116 A1##WO 2004/029201 A3##US 2005/0089840 A1##EP 1542718 A2##AP 2005003291 A0##BR 0314657 A##CN 1668330 A##EA 200500533 A1## JP 2006505536 A##ZA 200503118	Human immunodeficiency virus (HIV) gp41 peptide derivatives with enhanced solubility and antiviral activity	"The 'X' at position 35 represents a Lysine residue derivatized with a maleimide moiety.The peptide was modified with acetyl N-terminus and amide C-terminus, which exihibits antiviral activity by inhibiting viral infection of cells, for example, by inhibiting cell-cell fusion or free virus infection."	"This invention relates to gp41 peptide derivatives that are inhibitors of viral infection and/or exhibit antifusogenic properties. In particular, this invention relates to gp41 derivatives having inhibiting activity against human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV) with enhanced duration of action for the treatment of the respective viral infections."
DRAVP02452	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQQLLGI	60	Sequence 1 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02453	WNASWSNKSLEQIWNNMTWMEWDREINNYTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	64	Sequence 2 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02454	NNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	38	Sequence 3 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02455	YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 4 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02456	WQEWEQKITALLEQAQIQQEKNEYELQKLDKWASLWEWF	39	Sequence 5 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02457	GSTMGARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLT	43	Sequence 6 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02458	GSTMGARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARI	54	Sequence 7 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02459	GARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLL	36	Sequence 8 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02460	GARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQL	38	Sequence 9 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02461	GARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTV	40	Sequence 10 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02462	GARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARI	50	Sequence 11 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02463	ARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQ	36	Sequence 12 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02464	RSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQL	36	Sequence 13 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02465	SMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLT	36	Sequence 14 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02466	MTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLT	35	Sequence 15 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02467	MTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTV	36	Sequence 16 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02468	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLT	34	Sequence 17 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02469	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTV	35	Sequence 18 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02470	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVW	36	Sequence 19 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02471	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWG	37	Sequence 20 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02472	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGI	38	Sequence 21 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02473	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQAR	44	Sequence 22 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02474	LTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWG	36	Sequence 23 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02475	QARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARIL	42	Sequence 24 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02476	QARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERY	47	Sequence 25 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02477	QARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLK	49	Sequence 26 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02478	QARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	51	Sequence 27 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02479	SGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARIL	36	Sequence 28 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02480	SGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	45	Sequence 29 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02481	QQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	41	Sequence 30 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02482	RAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	34	Sequence 31 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02483	WMEWDREINNYTSLIHSLIEESQNQQEKNEQELLEL	36	Sequence 32 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02484	CGGNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	41	Sequence 33 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02485	NNLLRAIEAQQHLLQLTVWGIKQLQARILAV	31	Sequence 34 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02486	NNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQGGC	41	Sequence 35 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02487	CGGNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQGGC	44	Sequence 36 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02488	LSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAV	39	Sequence 37 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02489	YTNTIYTLLEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 38 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02490	YTGIIYNLLEESQNQQEKNEQELLELDKWANLWNWF	36	Sequence 39 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02491	YTSLIYSLLEKSQIQQEKNEQELLELDKWASLWNWF	36	Sequence 40 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02492	YTSLIHSLIEESQNQQEKNEQELLELDKWASLFNFF	36	Sequence 41 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02493	WQEWEQKVRYLEANITALLEQAQIQQEKNEYELQKL	36	Sequence 42 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02494	DREINNYTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	42	Sequence 43 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02495	MTWMEWDREINNYTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	48	Sequence 44 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02496	NNMTWMEWDREINNYTSLIHSLIEESQNQQEKNEQELLELDK	42	Sequence 45 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02497	WQEWEQKVRYLEANITALLEQAQIQQEKNEYELQKLDKWASLWNWF	46	Sequence 46 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02498	NNMTWQEWEQKVRYLEANITALLEQAQIQQEKNEYELQKLDKWASLWNWF	50	Sequence 47 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02499	WNWFITALLEQAQIQQEKNEYELQKLDKWASLWNWF	36	Sequence 48 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02500	WQEWDREISNYTSLITALLEQAQIQQEKNEYELQKLDEWASLWEWF	46	Sequence 49 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02501	WQEWEREISAYTSLITALLEQAQIQQEKIEYELQKLEWEW	40	Sequence 50 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02502	WQEWDREITALLEQAQIQQEKNEYELQKLDKWASLWNWF	39	Sequence 51 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02503	WQEWDREITALLEQAQIQQEKNEYELQKLDEWASLWEWF	39	Sequence 52 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02504	WQEWDREITALLEQAQIQQEKNEYELQKLDEWEWF	35	Sequence 53 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02505	WQEWEREITALLEQAQIQQEKIEYELQKLIEWEWF	35	Sequence 54 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02506	WQEWEREITALLEQAQIQQEKNEYELQKLIEWEWF	35	Sequence 55 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02507	WQEWEREITALLEQAQIQQEKIEYELQKLDEWEWF	35	Sequence 56 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02508	WQEWEQKITALLEQAQIQQEKNEYELQKLDKWASLWNWF	39	Sequence 57 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02509	WQEWEQKITALLEQAQIQQEKNEYELQKLDKWAGLWEWF	39	Sequence 58 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02510	WQEWEQKITALLEQAQIQQEKNEYELQKLAEWAGLWAWF	39	Sequence 59 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02511	WQEWEQKITALLEQAQIQQEKIEYELQKLIEWEWF	35	Sequence 60 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02512	QQQNNLLRAIEAQQHLLQLTAWGIKQLQARILAVERYLKDQ	41	Sequence 61 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02513	QQQNNLLRAIEAQQHLLQLTVAGIKQLQARILAVERYLKDQ	41	Sequence 62 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02514	QARQLLSGIVQQQNNLLRAIEAQQHALQATVWGIKQLQARILAVERYLK	49	Sequence 63 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02515	QARQLLSGIVQQQNNLLRAIEAQQHALQATVWGIKQLQARILAVERYLKDQ	51	Sequence 64 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02516	QARQLVSGLVQQQNNILRALEATQHAVQALVWGVKQLQARVLALERYIK	49	Sequence 65 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02517	QIRQLLSGIVQQQNNLLRAIEAIQHALQAIVWGIKQLQARILAVERYLK	49	Sequence 66 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02518	QARQLVSGLVQQQNNILRALEATQHAVQALVWGVRQLQARVLALERYIK	49	Sequence 67 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02519	QARQLLSGIVQQQNNLLRAIEATQHAVQALVWGVKQLQARVLALERYIKDQ	51	Sequence 68 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02520	QARQLVSGLVQQQNNILRALEAQQHALQATVWGIKQLQARVLALERYIKDQ	51	Sequence 69 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02521	QARQLLSGIVQQQNNLLRAIEAQQHALQATVWGVKQLQARILAVERYLKDQ	51	Sequence 70 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02522	QQQNNLLRAIEAQQHLLQLTVFGIKQLQARILAVERYLKDQ	41	Sequence 71 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02523	QARQLLSGIVQQQNNLLRAIEAQQHLLQLTVFGIRQLQARILAVERYLK	49	Sequence 72 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02524	QARQLLSGIVQQQNNLLRAIEAQQHLLQATVWGIKQLQARILAVERYLKDQ	51	Sequence 73 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02525	QQQNNLLRAIEAQQHLLQATVWGIKQLQARILAVERYLKDQ	41	Sequence 74 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02526	NASWSNKSLEQIWNNMTWMEWDREINNYTSLIHSLI	36	Sequence 75 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02527	NKSLEQIWNNMTWMEWDREINNYTSLIHSLIEESQN	36	Sequence 76 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02528	KSLEQIWNNMTWMEWDREINNYTSLIHSLIEESQNQ	36	Sequence 77 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02529	SLEQIWNNMTWMEWDREINNYTSLIHSLIEESQNQQ	36	Sequence 78 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02530	LEQIWNNMTWMEWDREINNYTSLIHSLIEESQNQQE	36	Sequence 79 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02531	EQIWNNMTWMEWDREINNYTSLIHSLIEESQNQQEK	36	Sequence 80 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02532	QIWNNMTWMEWDREINNYTSLIHSLIEESQNQQEKN	36	Sequence 81 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02533	IWNNMTWMEWDREINNYTSLIHSLIEESQNQQEKNE	36	Sequence 82 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02534	WNNMTWMEWDREINNYTSLIHSLIEESQNQQEKNEQ	36	Sequence 83 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02535	NNMTWMEWDREINNYTSLIHSLIEESQNQQEKNEQE	36	Sequence 84 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02536	NMTWMEWDREINNYTSLIHSLIEESQNQQEKNEQEL	36	Sequence 85 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02537	MTWMEWDREINNYTSLIHSLIEESQNQQEKNEQELL	36	Sequence 86 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02538	TWMEWDREINNYTSLIHSLIEESQNQQEKNEQELLE	36	Sequence 87 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02539	WMEWDREINNYTSLIHSLIEESQNQQEKNEQELLEL	36	Sequence 88 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02540	MEWDREINNYTSLIHSLIEESQNQQEKNEQELLED	35	Sequence 89 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02541	EWDREINNYTSLIHSLIEESQNQQEKNEQELLELDK	36	Sequence 90 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02542	WDREINNYTSLIHSLIEESQNQQEKNEQELLELDKW	36	Sequence 91 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02543	NYTSLIHSLIEESQNQQEKNEQELLELDKWASLWNW	36	Sequence 92 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02544	TSLIHSLIEESQNQQEKNEQELLELDKWASLWNWFN	36	Sequence 93 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02545	SLIHSLIEESQNQQEKNEQELLELDKWASLWNWFNI	36	Sequence 94 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02546	LIHSLIEESQNQQEKNEQELLELDKWASLWNWFNIT	36	Sequence 95 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02547	KSLEQIWNNMTWMEWEREIDNYTSLIYSLIEESQNQQEKNEQE	43	Sequence 96 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02548	NNMTWMEWEREIDNYTSLIYSLIEESQNQQEKNEQE	36	Sequence 97 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02549	EWEREIDNYTSLIYSLIEESQNQQEKNEQE	30	Sequence 98 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02550	SLEQIWNNMTWMEWEREIDNYTSLIYSLI	29	Sequence 99 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02551	LTWQEWDREINNYTSLIYSLIEESQNQQEENEQELL	36	Sequence 114 from Patent US 7556813 B2	Synthetic construct	HIV	Granted Patent	US 7556813 B2	2009-07-07	CA 2497767 A1##WO 2004/029073 A2##AU 2003/278937 A1##US 2004/0122214 A1##WO 2004/029073 A3##KR 20050046780 A##MX PA05003036 A##EP 1554306 A2##BR 0314707 A##RU 2005112729 A##CN 1684972 A##RU 2317997 C2	Antiviral peptide-polymer conjugate comprising a polymer covalently attached to two or more synthetic HIV gp41 HR1 and/or HR2 peptides	No comments found in patent	"Provided are conjugates comprising a polymer having operably bound thereto no less than two molecules of synthetic peptide derived from HIV gp41; methods of using these conjugates to inhibit transmission of HIV to a target cell by adding an amount of effective to inhibit infection of the cell by the virus; and methods of producing the conjugates by operably binding each molecule of synthetic peptide, via a reactive functionality, to the polymer."
DRAVP02552	RRKKAAVALLPAVLLALLAP	20	Sequence 1 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV).The peptide inhibits HSV-1 by blocking entry(IC50=15-26 ¦Ìm)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02553	RRKKAAVALLPAVLLALLAP	20	Sequence 2 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV).The peptide inhibits HSV-1 by blocking entry(IC50=15 ¦Ìm) and antifree virus activity(IC50=21 ¦Ìm)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02554	RRKKAAVALLAVLLALLAPP	20	Sequence 3 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02555	RRKKPAVLLALLA	13	Sequence 4 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02556	KLALKLALKALKAALKLA	18	Sequence 5 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV).The peptide inhibits HSV-1 by blocking entry(IC50=11 ¦Ìm) and antifree virus activity(IC50=4.5 ¦Ìm)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02557	KLALKLALKALKAALKLA	18	Sequence 6 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV).The peptide inhibits HSV-1 by blocking entry(IC50=23 ¦Ìm)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02558	RQIKIWFPNRRMKWKKPGYAGAVVNDL	27	Sequence 7 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV).The peptide inhibits HSV-1 by blocking entry(IC50=9-12 ¦Ìm) and antifree virus activity(IC50=6 ¦Ìm)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02559	RQIKIWFPNRRMKWKK	16	Sequence 8 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV).The peptide inhibits HSV-1 by blocking entry(IC50=7 ¦Ìm)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02560	RQIKIFFPNRRMKFKK	16	Sequence 9 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV).The peptide inhibits HSV-1 by blocking entry(IC50=40 ¦Ìm) and antifree virus activity(IC50=34 ¦Ìm)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02561	YGRKKRRQRRRPGYAGAVVNDL	22	Sequence 10 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV).The peptide inhibits HSV-1 by blocking entry(IC50=26 ¦Ìm) and antifree virus activity(IC50=8 ¦Ìm)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02562	YGRKKRRQRRRPGDVYANGLVA	22	Sequence 11 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV).The peptide inhibits HSV-1 by blocking entry(IC50=67 ¦Ìm)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02563	GWTLNSAGYLLGKINLKALAALAKKIL	27	Sequence 12 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02564	DPKGDPKGVTVTVTVTVTGKGDPKPD	26	Sequence 13 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02565	RRKK	4	Sequence 16 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02566	RRKKLAALPLVLAAPLAVLA	20	Sequence 17 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02567	RRKKAAVALLP	11	Sequence 18 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02568	RRKKAVAVAVPAVLLALLAP	20	Sequence 19 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02569	RRKKPAVLLA	10	Sequence 20 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02570	RRKKPAVLLALLALLA	16	Sequence 21 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02571	RRKKALLPAVLLALLAP	17	Sequence 22 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02572	RRKKPAVLLALLAP	14	Sequence 23 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02573	RRKKLLALLAP	11	Sequence 24 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02574	RRKKLLAP	8	Sequence 25 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02575	RRKKAAVALLPAVLLAL	17	Sequence 26 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02576	RRKKAAVAVVPAVL	14	Sequence 27 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02577	RRKKAAVAVVP	11	Sequence 28 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02578	RRKKAAVA	8	Sequence 29 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02579	GRKKRRQRRRPLAALPLVLAAPLAVLA	27	Sequence 30 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02580	YGRKKRRQRRRPLAALPLVLAAPLAVLA	28	Sequence 31 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02581	LAALPLVLAAPLAVLAPGRKKRRQRRRC	28	Sequence 32 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02582	LVLAAPLAVLAPGRKKRRQRRRC	23	Sequence 33 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02583	LAVLAPGRKKRRQRRRC	17	Sequence 34 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02584	GRKKRRQRRRC	11	Sequence 35 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02585	GRKKRRQRRR	10	Sequence 36 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02586	GRKKRRQRRR	10	Sequence 37 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02587	GRKKRRQRRRC	11	Sequence 38 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02588	GRKKRRQRRRC	11	Sequence 39 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02589	GRXXRRQRRRC	11	Sequence 40 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The 'X' at position 3 and 4 represents Norleucine.The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02590	GRKKRRQXXRC	11	Sequence 41 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The 'X' at position 8 and 9 represents Norleucine.The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02591	GRKKRRQXXRC	11	Sequence 42 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The 'X' at position 8 and 9 represents Norleucine.The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02592	PGYAGAVVNDL	11	Sequence 43 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02593	PGDVYANGLVA	11	Sequence 44 from Patent US 7432045 B2	Synthetic construct	"HSV,HIV,Influenza A Virus,H5 Avian Influenza Virus"	Granted Patent	US 7432045 B2	2008-10-07	WO 2005/060541 A2##US 2005/0203024 A1##WO 2005/060541 A3##US 7432045 B2	Method of inhibiting influenza infection with antiviral peptides	"The antiviral peptide showS antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesicular stomatitis virus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), influenza virus and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, papilloma virus (PV) and adenoviruses (AV)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and non-enveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP02594	YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 1 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	No comments found in patent	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02595	SSESFTLLEQWNNWKLQLAEQWLEQINEKHYLEDIS	36	Sequence 2 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	No comments found in patent	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02596	YTNTIYTLLEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 3 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	No comments found in patent	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02597	YTGIIYNLLEESQNQQEKNEQELLELDKWANLWNWF	36	Sequence 4 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	No comments found in patent	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02598	YTSLIYSLLEKSQTQQEKNEQELLELDKWASLWNWF	36	Sequence 5 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	No comments found in patent	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02599	LEANISKSLEQAQIQQEKNMYELQKLNSWDIFGNWF	36	Sequence 6 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	No comments found in patent	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02600	LEANISQSLEQAQIQQEKNMYELQKLNSWDVFTNWL	36	Sequence 7 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	No comments found in patent	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02601	CGGNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	41	Sequence 8 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	No comments found in patent	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02602	LQARILAVERYLKDQQQ	17	Sequence 9 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	No comments found in patent	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02603	QQLLDVVKRQQEMLRLTVWGTKNLQARVTAIEKYLKDQ	38	Sequence 10 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	No comments found in patent	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02604	YTSVITIELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	48	Sequence 16 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02605	FYDPLVFPSDEFDASISQVNEKINQSLAFIRKSDELL	37	Sequence 17 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02606	ITLNNSVALDPIDISIELNKAKSDLEESKEWIRRS	35	Sequence 18 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02607	ALGVATSAQITAAVALVEAKQARSDIEKLKEAIR	34	Sequence 19 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02608	VAVSKVLHLEGEVNKIALLSTNKAVVSLSNGVS	33	Sequence 20 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02609	AVSKVLHLEGEVNKIALLSTNKAVVSLSNGVSV	33	Sequence 21 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02610	VSKVLHLEGEVNKIALLSTNKAVVSLSNGVSVL	33	Sequence 22 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02611	SKVLHLEGEVNKIALLSTNKAVVSLSNGVSVLT	33	Sequence 23 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02612	KVLHLEGEVNKIALLSTNKAVVSLSNGVSVLTS	33	Sequence 24 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02613	LEGEVNKIALLSTNKAVVSLSNGVSVLTSKVLD	33	Sequence 25 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02614	GEVNKIALLSTNKAVVSLSNGVSVLTSKVLDLK	33	Sequence 26 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02615	EVNKIALLSTNKAVVSLSNGVSVLTSKVLDLKN	33	Sequence 27 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02616	VNKIALLSTNKAVVSLSNGVSVLTSKVLDLKNY	33	Sequence 28 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02617	NKIALLSTNKAVVSLSNGVSVLTSKVLDLKNYI	33	Sequence 29 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02618	KIALLSTNKAVVSLSNGVSVLTSKVLDLKNYID	33	Sequence 30 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02619	IALLSTNKAVVSLSNGVSVLTSKVLDLKNYIDK	33	Sequence 31 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02620	ALLSTNKAVVSLSNGVSVLTSKVLDLKNYIDKQ	33	Sequence 32 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02621	TLNNSVALDPIDISIELNKAKSDLEESKEWIRRSN	35	Sequence 33 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02622	LNNSVALDPIDISIELNKAKSDLEESKEWIRRSNQ	35	Sequence 34 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02623	NNSVALDPIDISIELNKAKSDLEESKEWIRRSNQK	35	Sequence 35 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02624	NSVALDPIDISIELNKAKSDLEESKEWIRRSNQKL	35	Sequence 36 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02625	SVALDPIDISIELNKAKSDLEESKEWIRRSNQKLD	35	Sequence 37 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02626	VALDPIDISIELNKAKSDLEESKEWIRRSNQKLDS	35	Sequence 38 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02627	ALDPIDISIELNKAKSDLEESKEWIRRSNQKLDSI	35	Sequence 39 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02628	LDPIDISIELNKAKSDLEESKEWIRRSNQKLDSIG	35	Sequence 40 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02629	DPIDISIELNKAKSDLEESKEWIRRSNQKLDSIGN	35	Sequence 41 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02630	PIDISIELNKAKSDLEESKEWIRRSNQKLDSIGNW	35	Sequence 42 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02631	IDISIELNKAKSDLEESKEWIRRSNQKLDSIGNWH	35	Sequence 43 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02632	DISIELNKAKSDLEESKEWIRRSNQKLDSIGNWHQ	35	Sequence 44 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02633	ISIELNKAKSDLEESKEWIRRSNQKLDSIGNWHQS	35	Sequence 45 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02634	SIELNKAKSDLEESKEWIRRSNQKLDSIGNWHQSS	35	Sequence 46 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02635	IELNKAKSDLEESKEWIRRSNQKLDSIGNWHQSST	35	Sequence 47 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02636	ELNKAKSDLEESKEWIRRSNQKLDSIGNWHQSSTT	35	Sequence 48 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02637	TAAVALVEAKQARSDIEKLKEAIRDTNKAVQSVQS	35	Sequence 49 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02638	AVALVEAKQARSDIEKLKEAIRDTNKAVQSVQSSI	35	Sequence 50 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02639	LVEAKQARSDIEKLKEAIRDTNKAVQSVQSSIGNL	35	Sequence 51 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02640	VEAKQARSDIEKLKEAIRDTNKAVQSVQSSIGNLI	35	Sequence 52 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02641	EAKQARSDIEKLKEAIRDTNKAVQSVQSSIGNLIV	35	Sequence 53 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02642	AKQARSDIEKLKEAIRDTNKAVQSVQSSIGNLIVA	35	Sequence 54 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02643	KQARSDIEKLKEAIRDTNKAVQSVQSSIGNLIVAI	35	Sequence 55 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02644	QARSDIEKLKEAIRDTNKAVQSVQSSIGNLIVAIK	35	Sequence 56 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02645	ARSDIEKLKEAIRDTNKAVQSVQSSIGNLIVAIKS	35	Sequence 57 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02646	RSDIEKLKEAIRDTNKAVQSVQSSIGNLIVAIKSV	35	Sequence 58 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02647	SDIEKLKEAIRDTNKAVQSVQSSIGNLIVAIKSVQ	35	Sequence 59 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02648	KLKEAIRDTNKAVQSVQSSIGNLIVAIKSVQDYVN	35	Sequence 60 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02649	LKEAIRDTNKAVQSVQSSIGNLIVAIKSVQDYVNK	35	Sequence 61 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02650	AIRDTNKAVQSVQSSIGNLIVAIKSVQDYVNKEIV	35	Sequence 62 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02651	WQEWERKVDFLEENITALLEEAQIQQEKNMYELQK	35	Sequence 63 from Patent US 6228983 B1	Synthetic construct	SIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02652	QEWERKVDFLEENITALLEEAQIQQEKNMYELQKL	35	Sequence 64 from Patent US 6228983 B1	Synthetic construct	SIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02653	EWERKVDFLEENITALLEEAQIQQEKNMYELQKLN	35	Sequence 65 from Patent US 6228983 B1	Synthetic construct	SIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02654	WERKVDFLEENITALLEEAQIQQEKNMYELQKLNS	35	Sequence 66 from Patent US 6228983 B1	Synthetic construct	SIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02655	ERKVDFLEENITALLEEAQIQQEKNMYELQKLNSW	35	Sequence 67 from Patent US 6228983 B1	Synthetic construct	SIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02656	RKVDFLEENITALLEEAQIQQEKNMYELQKLNSWD	35	Sequence 68 from Patent US 6228983 B1	Synthetic construct	SIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02657	KVDFLEENITALLEEAQIQQEKNMYELQKLNSWDV	35	Sequence 69 from Patent US 6228983 B1	Synthetic construct	SIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02658	VDFLEENITALLEEAQIQQEKNMYELQKLNSWDVF	35	Sequence 70 from Patent US 6228983 B1	Synthetic construct	SIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02659	DFLEENITALLEEAQIQQEKNMYELQKLNSWDVFG	35	Sequence 71 from Patent US 6228983 B1	Synthetic construct	SIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02660	FLEENITALLEEAQIQQEKNMYELQKLNSWDVFGN	35	Sequence 72 from Patent US 6228983 B1	Synthetic construct	SIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02661	LHRIDLGPPISLERLDVGTNLGNAIAKLEAKELL	34	Sequence 73 from Patent US 6228983 B1	Synthetic construct	MeV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02662	HRIDLGPPISLERLDVGTNLGNAIAKLEAKELLE	34	Sequence 74 from Patent US 6228983 B1	Synthetic construct	MeV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02663	RIDLGPPISLERLDVGTNLGNAIAKLEAKELLES	34	Sequence 75 from Patent US 6228983 B1	Synthetic construct	MeV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02664	IDLGPPISLERLDVGTNLGNAIAKLEAKELLESS	34	Sequence 76 from Patent US 6228983 B1	Synthetic construct	MeV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02665	DLGPPISLERLDVGTNLGNAIAKLEAKELLESSD	34	Sequence 77 from Patent US 6228983 B1	Synthetic construct	MeV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02666	LGPPISLERLDVGTNLGNAIAKLEAKELLESSDQ	34	Sequence 78 from Patent US 6228983 B1	Synthetic construct	MeV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02667	GPPISLERLDVGTNLGNAIAKLEAKELLESSDQI	34	Sequence 79 from Patent US 6228983 B1	Synthetic construct	MeV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02668	PPISLERLDVGTNLGNAIAKLEAKELLESSDQIL	34	Sequence 80 from Patent US 6228983 B1	Synthetic construct	MeV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02669	PISLERLDVGTNLGNAIAKLEAKELLESSDQILR	34	Sequence 81 from Patent US 6228983 B1	Synthetic construct	MeV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02670	SLERLDVGTNLGNAIAKLEAKELLESSDQILRSM	34	Sequence 82 from Patent US 6228983 B1	Synthetic construct	MeV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02671	LERLDVGTNLGNAIAKLEAKELLESSDQILRSMK	34	Sequence 83 from Patent US 6228983 B1	Synthetic construct	MeV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02672	MKQLEDKVEELLSKNYHLENEVARLKKL	28	Sequence 84 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02673	TDTLQAETDQLEDEKSALQTEIANLLKE	28	Sequence 85 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02674	IARLEEKVKTLKAQNSELASTANMLREQ	28	Sequence 86 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02675	EQKLISEEDLLEKRREQLKHKLEQLRNS	28	Sequence 87 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02676	IEKTNEKFHQIEKEFSEVEGRIQDLEKY	28	Sequence 88 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02677	NNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	38	Sequence 89 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02678	YTSVITIELSNIKENKCNGAKVKLIKQELDKYKNAVTELQLLMQST	46	Sequence 97 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02679	ASGVAVSKVLHLEGEVNKIALLSTNKAVVSLSNGVSVLTSKVLDLKNYIDKQLL	54	Sequence 98 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02680	GEPIINFYDPLVFPSDEFDASISQVNEKINQSLAFIRKSDELLHNVNAGKSTT	53	Sequence 99 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02681	GTIALGVATSAQITAAVALVEAKQARSDIEKLKEAIRDTNKAVQSVQSSIGNLIVAIKSVQDYVNKEIVP	70	Sequence 100 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02682	YTPNDITLNNSVALDPIDISIELNKAKSDLEESKEWIRRSNQKLDSIGNWHQSSTT	56	Sequence 101 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02683	PDAVYLHRIDLGPPISLERLDVGTNLGNAIAKLED	35	Sequence 118 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02684	LERLDVGTNLGNAIAKLEAKELLESSDQILRSMK	34	Sequence 119 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02685	TWQEWERKVDFLEENITALLEEAQIQQEKNMYELQKLNSWDVFGNWF	47	Sequence 120 from Patent US 6228983 B1	Synthetic construct	SIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02686	IELSNIKENKCNGTDAKVKLIKQELDKYKNAVTELQLLMQST	42	Sequence 121 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group. The antiviral activity of peptide on RSV(IC50>500 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02687	VSKGYSALRTGWYTSVITIELSNIKEN	27	Sequence 122 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group. The antiviral activity of peptide on RSV(IC50=165 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02688	AFIRKSDELLHNV	13	Sequence 123 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50=26 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02689	YTSVITIELSNIKENKXNGTDAKVKLIKQELDKYK	35	Sequence 124 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50>500 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02690	TSVITIELSNIKENKXNGTDAKVKLIKQELDKYKN	35	Sequence 125 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02691	SVITIELSNIKENKXNGTDAKVKLIKQELDKYKNA	35	Sequence 126 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50>500 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02692	SNIKENKXNGTDAKVKLIKQELDKYKNAVTELQLL	35	Sequence 127 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50>500 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02693	KENKXNGTDAKVKLIKQELDKYKNAVTELQLLMQS	35	Sequence 128 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50>500 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02694	AVSKGYLSALRTGWYTSVITIELSNIKENKXNGTDA	36	Sequence 129 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50>100 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02695	VVSLSNGVSVLTSKVLDLKNYIDKQLL	27	Sequence 130 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50>500 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02696	LLSTNKAVVSLSNGVSVLTSKVLDLKNY	28	Sequence 131 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50>500 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02697	VLHLEGEVNKIKSALLSTNKAVVSLSNG	28	Sequence 132 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50>500 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02698	LLSTNKAVVSLSNGVSVLTSKVLDLKNY	28	Sequence 133 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50>500 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02699	ASGVAVSKVLHLEGEVNKIKSALLSTNKAVVSLSNGV	37	Sequence 134 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50>500 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02700	VLHLEGEVNKIKSALLSTNKAVVSLSNGVSVLTSK	35	Sequence 135 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50=328 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02701	NDQKKLMSNNVQIVRQQSYSIMSIIKEE	28	Sequence 136 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50>500 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02702	SISNIETVIEFQQKNNRLLEITREFSVNAGVTTPVS	36	Sequence 137 from Patent US 6228983 B1	Synthetic construct	RSV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group.The antiviral activity of peptide on RSV(IC50>100 ¦Ìg/ml)."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02703	PIINFYDPLVFPSDEFDASISQVNEKINQSLAFIR	35	Sequence 138 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02704	RMKQLEDKVEELLSKLAFIRKSDELLHNV	29	Sequence 139 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02705	AFIRKSDELLHNVNAGKST	19	Sequence 140 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02706	FDASISQVNEKINQSLAFI	19	Sequence 141 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02707	SLAFIRKSDELLHNVNAGKST	21	Sequence 142 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02708	FDASISQVNEKINQSLAFIRKSDELLHNVNAGK	33	Sequence 143 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02709	ASISQVNEKINQSLAFIRKSDELLHNVNAGKST	33	Sequence 144 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02710	FDASISQVNEKINQSLAFIRKSDELLHNVNAGKST	35	Sequence 145 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02711	ATSAQITAAVALVEAKQARSDIEKLKEA	28	Sequence 146 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02712	AAVALVEAKQARSDIEKLKEAIRDTNKAVQSVQSS	35	Sequence 147 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02713	AKQARSDIEKLKEAIRDTNKAVQSVQSSIGNLIVA	35	Sequence 148 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02714	IRDTNKAVQSVQSSIGNLIVAIKSVQDY	28	Sequence 149 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02715	AVQSVQSSIGNLIVAIKSVQDYVNKEIV	28	Sequence 150 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02716	LKEAIRDTNKAVQSVQSSIGNLIVAIKS	28	Sequence 151 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02717	EWIRRSNQKLDSI	13	Sequence 152 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02718	IDISIELNKAKSDLEESKEWIKKSNQKLDSIGNWH	35	Sequence 153 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02719	RMKQLEDKVEELLSKLEWIRRSNQKLDSI	29	Sequence 154 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02720	DQQIKQYKRLLDRLIIPLYDGLRQKDVIVSNQESN	35	Sequence 155 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02721	YSELTNIFGDNIGSLQEKGIKLQGIASLYRTNITEI	36	Sequence 156 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02722	TSITLQVRLPLLTRLLNTQIYRVDSISYNIQNREWY	36	Sequence 157 from Patent US 6228983 B1	Synthetic construct	HPIV3	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02723	NKSLEQIWNNMTWMEWDREINNYTSLIHSLIEEQNQQEKNEQELLELDKWASLWNWF	57	Sequence 158 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02724	WMEWDREINNYTSLIGSLIEESQNQQEKNEQELLE	35	Sequence 159 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02725	YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWFNITNWLWLIKIFI	49	Sequence 160 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02726	EAAAREAAAREAAARLELDKWASLWNWF	28	Sequence 161 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02727	RMKQLEDKVEELLSKLELDKWASLWNWF	28	Sequence 162 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02728	FWNWLSAWKDLELKSLLEEVKDELQKMR	28	Sequence 163 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02729	RMKQLEDKVEELLSKNYHLENELELDKWASLWNWF	35	Sequence 164 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02730	FWNWLSAWKDLELYPGSLELDKWASLWNWF	30	Sequence 165 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02731	CLELDKWASLWNWFC	15	Sequence 166 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02732	CLELDKWASLANWFC	15	Sequence 167 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02733	CLELDKWASLWNFFC	15	Sequence 168 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02734	LELDKWASLANAF	13	Sequence 169 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02735	LELDKWASLFNFF	13	Sequence 170 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02736	LELDKWASLWNAF	13	Sequence 171 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02737	LELDKWASLWNWA	13	Sequence 172 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02738	LELDKWASAWNWF	13	Sequence 173 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02739	LELDKAASLWNWF	13	Sequence 174 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02740	LKLDKWASLWNWF	13	Sequence 175 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02741	LELKKWASLWNWF	13	Sequence 176 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02742	CGGYTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	39	Sequence 177 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02743	YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNAF	36	Sequence 178 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02744	YTSLIHSLIEESQNQQEKNEQELLELDKWASLANWF	36	Sequence 179 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02745	YTSLIHSLIEESQNQQEKNEQQLLELDKWASLWNWF	36	Sequence 180 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02746	YTSLIHSLIEESQNQQEKNEQELLQLDKWASLWNWF	36	Sequence 181 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02747	YTSLIHSLIEESQNQQEKNQQELLQLDKWASLWNWF	36	Sequence 182 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02748	YTSLIQSLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 183 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02749	YTSLIHSLIEESQQQQEKNEQELLELDKWASLWNWF	36	Sequence 184 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02750	YTSLIHSLIEESQNQQEKNEQELLELNKWASLWNWF	36	Sequence 185 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02751	YTSLIHSLIEQSQNQQEKNEQELLELDKWASLWNWF	36	Sequence 186 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02752	YTSLIHSLIQESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 187 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02753	YTSLIHSLIQQSQNQQQKNQQQLLQLDKWASLWNWF	36	Sequence 188 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02754	YTSLIHSLIEESQNQQEKNEQELLELDKWASLANAA	36	Sequence 189 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02755	YTSLIHSLIEESQNQQEKNEQQLLELDKWASLWNWF	36	Sequence 190 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02756	YTSLIQSLIEESQNQQEKNEQQLLELDKWASLWNWF	36	Sequence 191 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02757	YTSLIHSLIEESQNQQEKNEQELLELDKWASLFNFF	36	Sequence 192 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02758	YTSLIHSLIEESQNLQEKNEQELLELDKWASLWNWF	36	Sequence 193 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02759	YTSLIHSLIEESQNQQEKLEQELLELDKWASLWNWF	36	Sequence 194 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02760	YTSLIHSLIEESQNQQEKNEQELLEFDKWASLWNWF	36	Sequence 195 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02761	YTSLIHSLIEESQNQQEKNEQELLELDKPASLWNWF	36	Sequence 196 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02762	YTSLIHSLIEESQNQQEKNEQELLELDKWASPWNWF	36	Sequence 197 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02763	YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNSF	36	Sequence 198 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02764	LLDNFESTWEQSKELWEQQEISIQNLHKSALQEYWN	36	Sequence 199 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02765	LSNLLQISNNSDEWLEALEIEHEKWKLTQWQSYEQF	36	Sequence 200 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02766	MTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQQLLGIWG	63	Sequence 201 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02767	SELEIKRYKNRVASRKCRAKFQLLQHYREVAAAKSSENDRLRLLL	45	Sequence 202 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02768	ASRKCRAKFKQLLQHYREVAAAKSSENDRLRLLLKQMCPSLDVDS	45	Sequence 203 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02769	LLQHYREVAAAKSSENDRLRLLLKQMCPSLDVDSI	35	Sequence 204 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02770	LQHYREVAAAKSSENDRLRLLLKQMCPSLDVDSIIPRTPDVLHED	45	Sequence 205 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02771	SSENDRLRLLLKQMCPSLDVDSIIPRTPDVLHEDL	35	Sequence 206 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02772	SENDRLRLLLKQMCPSLDVDSIIPRTPDVLHEDLLNF	37	Sequence 207 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02773	PLLVLQAGFFLLTRILTIPQSLDSWWTSLNFLGGTTVCLGQNSQSP	46	Sequence 208 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02774	PGYRWMCLRRFIIFLFILLLCLIFLLVLLDYQGMLPVCPLIPGSSTSTGPCRTCMTT	57	Sequence 209 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02775	VITIELSNIKENKCNGTDAKVKLIKQELDKYKNAV	35	Sequence 210 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02776	DEFDASISQVNEKINQSLAFIRKSDELL	28	Sequence 211 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02777	IINFYDPLVFPSDEFDASISQVNEKINQSLAFIRK	35	Sequence 212 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02778	INFYDPLVFPSDEFDASISQVNEKINQSLAFIRKS	35	Sequence 213 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02779	FYDPLVFPSDEFDASISQVNEKINQSLAFIRKSDE	35	Sequence 214 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02780	YDPLVFPSDEFDASISQVNEKINQSLAFIRKSDEL	35	Sequence 215 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02781	DPLVFPSDEFDASISQVNEKINQSLAFIRKSDELL	35	Sequence 216 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02782	PLVFPSDEFDASISQVNEKINQSLAFIRKSDELLH	35	Sequence 217 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02783	LVFPSDEFDASISQVNEKINQSLAFIRKSDELLHN	35	Sequence 218 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02784	VFPSDEFDASISQVNEKINQSLAFIRKSDELLHNV	35	Sequence 219 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02785	FPSDEFDASISQVNEKINQSLAFIRKSDELLHNVN	35	Sequence 220 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02786	PSDEFDASISQVNEKINQSLAFIRKSDELLHNVNA	35	Sequence 221 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02787	SDEFDASISQVNEKINQSLAFIRKSDELLHNVNAG	35	Sequence 222 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02788	DEFDASISQVNEKINQSLAFIRKSDELLHNVNAGK	35	Sequence 223 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02789	EFDASISQVNEKINQSLAFIRKSDELLHNVNAGKS	35	Sequence 224 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02790	FDASISQVNEKINQSLAFIRKSDELLHNVNAGKST	35	Sequence 225 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02791	DASISQVNEKINQSLAFIRKSDELLHNVNAGKSTT	35	Sequence 226 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02792	FDASISQVNEKINQSLAFIRKSDELLHNVNA	31	Sequence 227 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02793	FDASISQVNEKINQSLAFIRKSDELLHNV	29	Sequence 228 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02794	FDASISQVNEKINQSLAFIRKSDELLH	27	Sequence 229 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02795	FDASISQVNEKINQSLAFIRKSDEL	25	Sequence 230 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02796	ISQVNEKINQSLAFIRKSDELLHNVNAGKST	31	Sequence 231 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02797	QVNEKINQSLAFIRKSDELLHNVNAGKST	29	Sequence 232 from Patent US 6228983 B1	Synthetic construct	HIV	Granted Patent	US 6228983 B1	2001-05-08	WO 1996/019495 A1##CA 2208420 A1##AU 1996/044734 A##EP 0793675 A1##KR 987000333 A##EP 0793675 A4##AU 714695 B2##US 6013263 A##NZ 300002 A##US 6054265 A##US 6060065 A##US 6068973 A##US 6093794 A##US 62	Human respiratory syncytial virus peptides with antifusogenic and antiviral activities	"The N teminal may be modified with an amino group,a hydrophobic group, an acetyl group, a 9-fluorenylmethoxycarbonyl group, or a macromolecular carrier group, and the C terminal may be modified with a carboxyl group, an amido group, a T-butyloxycarbonyl group, or a macromolecular carrier group."	"The present invention relates to peptides which exhibit antifusogenic and antiviral activities. The peptides of the invention consist of a 16 to 39 amino acid region of a human respiratory syncytial virus protein. These regions were identified through computer algorithms capable of recognizing the ALLMOTI5, 107x178x4, or PLZIP amino acid motifs. These motifs are associated with the antifusogenic and antiviral activities of the claimed peptides."
DRAVP02798	APGDEPAPPY	10	Sequence 3 from Patent US 5859187 A	Synthetic construct	HSV	Granted Patent	US 5859187 A	1999-01-12	IT 9019881 D0##GB 9007137 D0##CA 2011884 A1##DE 4010593 A1##FR 2645157 A1##GB 2230011 A##JP H0341094 A##IT 9019881 A1##US 5120639 A##GB 2230011 B##IT 1241092 B##FR 2645157 B1##US 5859187 A	Antiviral peptides	The peptide inhibits HSV by UL42 of HSV DNA polymerase(IC50=161 ¦ÌM).	Inhibition of UL42 stimulation of herpesvirus DNA polymerase activity is exhibited by novel compounds of the formulas EQU W'--A.sub.1 --A.sub.2 --A.sub.3 --A.sub.4 --A.sub.5 --A.sub.6 --A.sub.7 --A.sub.8 --A.sub.9 --A.sub.10 --A.sub.11 --X ?SEQ. ID NO: 1! and EQU Y'--A.sub.12 --A.sub.13 --A.sub.14 --A.sub.15 --A.sub.16 --A.sub.17 --Z ?SEQ. ID NO: 2! that are useful as antiviral agents.
DRAVP02799	APGDEPAPP	9	Sequence 4 from Patent US 5859187 A	Synthetic construct	HSV	Granted Patent	US 5859187 A	1999-01-12	IT 9019881 D0##GB 9007137 D0##CA 2011884 A1##DE 4010593 A1##FR 2645157 A1##GB 2230011 A##JP H0341094 A##IT 9019881 A1##US 5120639 A##GB 2230011 B##IT 1241092 B##FR 2645157 B1##US 5859187 A	Antiviral peptides	The peptide inhibits HSV by UL42 of HSV DNA polymerase(IC50=188 ¦ÌM).	Inhibition of UL42 stimulation of herpesvirus DNA polymerase activity is exhibited by novel compounds of the formulas EQU W'--A.sub.1 --A.sub.2 --A.sub.3 --A.sub.4 --A.sub.5 --A.sub.6 --A.sub.7 --A.sub.8 --A.sub.9 --A.sub.10 --A.sub.11 --X ?SEQ. ID NO: 1! and EQU Y'--A.sub.12 --A.sub.13 --A.sub.14 --A.sub.15 --A.sub.16 --A.sub.17 --Z ?SEQ. ID NO: 2! that are useful as antiviral agents.
DRAVP02800	AAPGDEPAPP	10	Sequence 5 from Patent US 5859187 A	Synthetic construct	HSV	Granted Patent	US 5859187 A	1999-01-12	IT 9019881 D0##GB 9007137 D0##CA 2011884 A1##DE 4010593 A1##FR 2645157 A1##GB 2230011 A##JP H0341094 A##IT 9019881 A1##US 5120639 A##GB 2230011 B##IT 1241092 B##FR 2645157 B1##US 5859187 A	Antiviral peptides	The peptide inhibits HSV by UL42 of HSV DNA polymerase(IC50=152 ¦ÌM).	Inhibition of UL42 stimulation of herpesvirus DNA polymerase activity is exhibited by novel compounds of the formulas EQU W'--A.sub.1 --A.sub.2 --A.sub.3 --A.sub.4 --A.sub.5 --A.sub.6 --A.sub.7 --A.sub.8 --A.sub.9 --A.sub.10 --A.sub.11 --X ?SEQ. ID NO: 1! and EQU Y'--A.sub.12 --A.sub.13 --A.sub.14 --A.sub.15 --A.sub.16 --A.sub.17 --Z ?SEQ. ID NO: 2! that are useful as antiviral agents.
DRAVP02801	AAAPGDEPAPP	11	Sequence 6 from Patent US 5859187 A	Synthetic construct	HSV	Granted Patent	US 5859187 A	1999-01-12	IT 9019881 D0##GB 9007137 D0##CA 2011884 A1##DE 4010593 A1##FR 2645157 A1##GB 2230011 A##JP H0341094 A##IT 9019881 A1##US 5120639 A##GB 2230011 B##IT 1241092 B##FR 2645157 B1##US 5859187 A	Antiviral peptides	The peptide inhibits HSV by UL42 of HSV DNA polymerase(IC50=90 ¦ÌM).	Inhibition of UL42 stimulation of herpesvirus DNA polymerase activity is exhibited by novel compounds of the formulas EQU W'--A.sub.1 --A.sub.2 --A.sub.3 --A.sub.4 --A.sub.5 --A.sub.6 --A.sub.7 --A.sub.8 --A.sub.9 --A.sub.10 --A.sub.11 --X ?SEQ. ID NO: 1! and EQU Y'--A.sub.12 --A.sub.13 --A.sub.14 --A.sub.15 --A.sub.16 --A.sub.17 --Z ?SEQ. ID NO: 2! that are useful as antiviral agents.
DRAVP02802	AGATAEETAY	10	Sequence 7 from Patent US 5859187 A	Synthetic construct	HSV	Granted Patent	US 5859187 A	1999-01-12	IT 9019881 D0##GB 9007137 D0##CA 2011884 A1##DE 4010593 A1##FR 2645157 A1##GB 2230011 A##JP H0341094 A##IT 9019881 A1##US 5120639 A##GB 2230011 B##IT 1241092 B##FR 2645157 B1##US 5859187 A	Antiviral peptides	The peptide inhibits HSV by UL42 of HSV DNA polymerase(IC50=37.5 ¦ÌM).	Inhibition of UL42 stimulation of herpesvirus DNA polymerase activity is exhibited by novel compounds of the formulas EQU W'--A.sub.1 --A.sub.2 --A.sub.3 --A.sub.4 --A.sub.5 --A.sub.6 --A.sub.7 --A.sub.8 --A.sub.9 --A.sub.10 --A.sub.11 --X ?SEQ. ID NO: 1! and EQU Y'--A.sub.12 --A.sub.13 --A.sub.14 --A.sub.15 --A.sub.16 --A.sub.17 --Z ?SEQ. ID NO: 2! that are useful as antiviral agents.
DRAVP02803	AGATAEETAA	10	Sequence 8 from Patent US 5859187 A	Synthetic construct	HSV	Granted Patent	US 5859187 A	1999-01-12	IT 9019881 D0##GB 9007137 D0##CA 2011884 A1##DE 4010593 A1##FR 2645157 A1##GB 2230011 A##JP H0341094 A##IT 9019881 A1##US 5120639 A##GB 2230011 B##IT 1241092 B##FR 2645157 B1##US 5859187 A	Antiviral peptides	The peptide inhibits HSV by UL42 of HSV DNA polymerase(IC50=56.6 ¦ÌM).	Inhibition of UL42 stimulation of herpesvirus DNA polymerase activity is exhibited by novel compounds of the formulas EQU W'--A.sub.1 --A.sub.2 --A.sub.3 --A.sub.4 --A.sub.5 --A.sub.6 --A.sub.7 --A.sub.8 --A.sub.9 --A.sub.10 --A.sub.11 --X ?SEQ. ID NO: 1! and EQU Y'--A.sub.12 --A.sub.13 --A.sub.14 --A.sub.15 --A.sub.16 --A.sub.17 --Z ?SEQ. ID NO: 2! that are useful as antiviral agents.
DRAVP02804	GATAEETA	8	Sequence 9 from Patent US 5859187 A	Synthetic construct	HSV	Granted Patent	US 5859187 A	1999-01-12	IT 9019881 D0##GB 9007137 D0##CA 2011884 A1##DE 4010593 A1##FR 2645157 A1##GB 2230011 A##JP H0341094 A##IT 9019881 A1##US 5120639 A##GB 2230011 B##IT 1241092 B##FR 2645157 B1##US 5859187 A	Antiviral peptides	The peptide inhibits HSV by UL42 of HSV DNA polymerase(IC50=240 ¦ÌM).	Inhibition of UL42 stimulation of herpesvirus DNA polymerase activity is exhibited by novel compounds of the formulas EQU W'--A.sub.1 --A.sub.2 --A.sub.3 --A.sub.4 --A.sub.5 --A.sub.6 --A.sub.7 --A.sub.8 --A.sub.9 --A.sub.10 --A.sub.11 --X ?SEQ. ID NO: 1! and EQU Y'--A.sub.12 --A.sub.13 --A.sub.14 --A.sub.15 --A.sub.16 --A.sub.17 --Z ?SEQ. ID NO: 2! that are useful as antiviral agents.
DRAVP02805	AGATAEETA	9	Sequence 10 from Patent US 5859187 A	Synthetic construct	HSV	Granted Patent	US 5859187 A	1999-01-12	IT 9019881 D0##GB 9007137 D0##CA 2011884 A1##DE 4010593 A1##FR 2645157 A1##GB 2230011 A##JP H0341094 A##IT 9019881 A1##US 5120639 A##GB 2230011 B##IT 1241092 B##FR 2645157 B1##US 5859187 A	Antiviral peptides	The peptide inhibits HSV by UL42 of HSV DNA polymerase(IC50=88.5 ¦ÌM).	Inhibition of UL42 stimulation of herpesvirus DNA polymerase activity is exhibited by novel compounds of the formulas EQU W'--A.sub.1 --A.sub.2 --A.sub.3 --A.sub.4 --A.sub.5 --A.sub.6 --A.sub.7 --A.sub.8 --A.sub.9 --A.sub.10 --A.sub.11 --X ?SEQ. ID NO: 1! and EQU Y'--A.sub.12 --A.sub.13 --A.sub.14 --A.sub.15 --A.sub.16 --A.sub.17 --Z ?SEQ. ID NO: 2! that are useful as antiviral agents.
DRAVP02806	EETRRMLHRAFDTLA	15	Sequence 11 from Patent US 5859187 A	Synthetic construct	HSV	Granted Patent	US 5859187 A	1999-01-12	IT 9019881 D0##GB 9007137 D0##CA 2011884 A1##DE 4010593 A1##FR 2645157 A1##GB 2230011 A##JP H0341094 A##IT 9019881 A1##US 5120639 A##GB 2230011 B##IT 1241092 B##FR 2645157 B1##US 5859187 A	Antiviral peptides	The peptide inhibits HSV by UL42 of HSV DNA polymerase(IC50=32.5 ¦ÌM).	Inhibition of UL42 stimulation of herpesvirus DNA polymerase activity is exhibited by novel compounds of the formulas EQU W'--A.sub.1 --A.sub.2 --A.sub.3 --A.sub.4 --A.sub.5 --A.sub.6 --A.sub.7 --A.sub.8 --A.sub.9 --A.sub.10 --A.sub.11 --X ?SEQ. ID NO: 1! and EQU Y'--A.sub.12 --A.sub.13 --A.sub.14 --A.sub.15 --A.sub.16 --A.sub.17 --Z ?SEQ. ID NO: 2! that are useful as antiviral agents.
DRAVP02807	APGDEPAPP	9	Sequence 12 from Patent US 5859187 A	Synthetic construct	HSV	Granted Patent	US 5859187 A	1999-01-12	IT 9019881 D0##GB 9007137 D0##CA 2011884 A1##DE 4010593 A1##FR 2645157 A1##GB 2230011 A##JP H0341094 A##IT 9019881 A1##US 5120639 A##GB 2230011 B##IT 1241092 B##FR 2645157 B1##US 5859187 A	Antiviral peptides	The peptide inhibits HSV by UL42 of HSV DNA polymerase(IC50=115 ¦ÌM).	Inhibition of UL42 stimulation of herpesvirus DNA polymerase activity is exhibited by novel compounds of the formulas EQU W'--A.sub.1 --A.sub.2 --A.sub.3 --A.sub.4 --A.sub.5 --A.sub.6 --A.sub.7 --A.sub.8 --A.sub.9 --A.sub.10 --A.sub.11 --X ?SEQ. ID NO: 1! and EQU Y'--A.sub.12 --A.sub.13 --A.sub.14 --A.sub.15 --A.sub.16 --A.sub.17 --Z ?SEQ. ID NO: 2! that are useful as antiviral agents.
DRAVP02808	CATCEQIADSQHRSHRQMV	19	Sequence 1 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02809	CATCEQIADSQHRSHRQMV	19	Sequence 2 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02810	CATCEQIADSQHRSHRQM	18	Sequence 3 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02811	CATCEQIADSQHRSHRQ	17	Sequence 4 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02812	CATCEQIADSQHRSHR	16	Sequence 5 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02813	CATCEQIADSQHRSH	15	Sequence 6 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02814	CATCQIADSQHRSHRQMV	18	Sequence 7 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02815	CATCIADSQHRSHRQMV	17	Sequence 8 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02816	CATCADSQHRSHRQMV	16	Sequence 9 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02817	CTCEQIADSQHRSHRQMV	18	Sequence 10 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02818	CACEQIADSQHRSHRQMV	18	Sequence 11 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02819	CATCEQIADSQHRHRQMV	18	Sequence 12 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02820	CATCEQIADSQHRHRQMV	18	Sequence 13 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	The peptide was modified with acetyl N-terminus.	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02821	CATCEQIADSQHRSHRQMV	19	Sequence 14 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	The peptide was modified with acetyl N-terminus and amide C-terminus.	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02822	CATCEQIADSQHRSHRQMV	19	Sequence 15 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02823	CAACEQIADSQHRSHRQMV	19	Sequence 16 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02824	CATCAQIADSQHRSHRQMV	19	Sequence 17 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02825	CATCEAIADSQHRSHRQMV	19	Sequence 18 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02826	CATCEQAADSQHRSHRQMV	19	Sequence 19 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02827	CATCEQIAASQHRSHRQMV	19	Sequence 20 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02828	CATCEQIADAQHRSHRQMV	19	Sequence 21 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02829	CATCEQIADSAHRSHRQMV	19	Sequence 22 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02830	CATCEQIADSQHASHRQMV	19	Sequence 23 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02831	CATCEQIADSQHRAHRQMV	19	Sequence 24 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02832	CATCEQIADSQHRSHAQMV	19	Sequence 25 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02833	CATCEQIADSQHRSHRAMV	19	Sequence 26 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02834	CATCEQIADSQHRSHRQAV	19	Sequence 27 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02835	CATCEQIADSQHRSHRQMA	19	Sequence 28 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02836	CATCEQIADSQHKSHRQMV	19	Sequence 29 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02837	CATCEQIADSQHRSHKQMV	19	Sequence 30 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02838	CATCEQIADSQHKSHKQMV	19	Sequence 31 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02839	CASCEQIADSQHRSHRQMV	19	Sequence 32 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02840	CATCDQIADSQHRSHRQMV	19	Sequence 33 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02841	CATCENIADSQHRSHRQMV	19	Sequence 34 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02842	CATCEQLADSQHRSHRQMV	19	Sequence 35 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02843	CATCEQVADSQHRSHRQMV	19	Sequence 36 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02844	CATCEQIAESQHRSHRQMV	19	Sequence 37 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02845	CATCEQIADTQHRSHRQMV	19	Sequence 38 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02846	CATCEQIADSNHRSHRQMV	19	Sequence 39 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02847	CATCEQIADSQHRTHRQMV	19	Sequence 40 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02848	CATCEQIADSQHRSHRNMV	19	Sequence 41 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02849	CATCEQIADSQHRSHRQML	19	Sequence 42 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02850	CATCEQIADSQHRSHRQMI	19	Sequence 43 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02851	CXTCEQIADSQHRSHRQMV	19	Sequence 44 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	The 'X' at position 2 represents D-Ala.	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02852	CATCEQIADSQHXSHRQMV	19	Sequence 45 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	The 'X' at position 13 represents D-Arg.	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02853	CATCEQIADSQHRSHXQMV	19	Sequence 46 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	The 'X' at position 16 represents D-Arg.	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02854	CXTCEQIADSQHXSHRQMV	19	Sequence 47 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	The 'X' at position 2 and 13 represent D-Ala and D-Arg.	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02855	CXTCEQIADSQHXSHXQMV	19	Sequence 48 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	The 'X' at position 2 represents D-Ala and 'X' at position 13 and 16 indicates D-Arg.	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02856	CXTCEQIADSQHRSHRQMV	19	Sequence 49 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	The 'X' at position 2 represents NMe-Ala.	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02857	CATCEQIADSQHXSHRQMV	19	Sequence 50 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	The 'X' at position 13 represents Nme-Arg.	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02858	CATCEQIADSQHRSHXQMV	19	Sequence 51 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	The 'X' at position 16 represents NMe-Arg.	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02859	CXTCEQIADSQHXSHRQMV	19	Sequence 52 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	The 'X' at position 2 and 13 represent NMe-Ala and NMe-Arg.	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02860	CXTCEQIADSQHXSHXQMV	19	Sequence 53 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	The 'X' at position 2 represents NMe-Ala and 'X' at position 13 and 16 indicates NMe-Arg.	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02861	LTVPSERGLQRRR	13	Sequence 54 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02862	ALNGNGDPNNMDKAVKLY	18	Sequence 55 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02863	KREITFHGAKEISLS	15	Sequence 56 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02864	EQIADSQHRSHRQMV	15	Sequence 57 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02865	GTHPSSSAGLKNDLLEN	17	Sequence 58 from Patent US 5616327	Synthetic construct	influenza virus	Granted Patent	US 5616327 A	1997-04-01	CA 2108263 A1##WO 1992/022575 A1##EP 0590055 A1##JP H06508623 A##US 5616327 A##EP 0590055 B1##DE 69223406 D1##DE 69223406 T2	M-protein peptides of influenza virus as antiviral agents	No comments found in patent	Peptides substantially corresponding to the 148-162 region of type A influenza M protein and additionally containing at least one amino acid in the 163-166 region are disclosed to have high activity as influenza transcription inhibitors and thus as antiviral agents against influenza virus and other RNA viruses. The modification of these peptides by incorporation into liposomes or by addition of long-chain alkylamino acids is also shown as in the use of all such materials in antiviral drug formulations.
DRAVP02866	TKPKTKPK	8	Sequence 1 from Patent US 5447915 A	Synthetic construct	HIV	Granted Patent	US 5447915 A	1995-09-05	CA 2077088 A1##WO 1991/013088 A1##US 5115098 A##EP 0517792 A1##JP H05503535 A##US 5447915 A	Terminally blocked antiviral peptides	No comments found in patent	This invention relates to antiviral peptide compounds and to methods of inhibiting infection of human cells by viruses. This invention pertains more specifically to peptides that are chemically blocked at the amino- and carboxy-termini. In particular the invention relates to peptides comprised of prolylalanine or prolylphenylalanine compounds that have antiviral activity. The invention is specifically directed to methods for preventing infection of human cells in vivo and in vitro with the human immunodeficiency virus HIV-1 and methods for treating human infected with this and other viruses. The invention also relates to the diagnostic and therapeutic use of these antiviral peptide compounds.
DRAVP02867	TKPKTKPR	8	Sequence 2 from Patent US 5447915 A	Synthetic construct	HIV	Granted Patent	US 5447915 A	1995-09-05	CA 2077088 A1##WO 1991/013088 A1##US 5115098 A##EP 0517792 A1##JP H05503535 A##US 5447915 A	Terminally blocked antiviral peptides	No comments found in patent	This invention relates to antiviral peptide compounds and to methods of inhibiting infection of human cells by viruses. This invention pertains more specifically to peptides that are chemically blocked at the amino- and carboxy-termini. In particular the invention relates to peptides comprised of prolylalanine or prolylphenylalanine compounds that have antiviral activity. The invention is specifically directed to methods for preventing infection of human cells in vivo and in vitro with the human immunodeficiency virus HIV-1 and methods for treating human infected with this and other viruses. The invention also relates to the diagnostic and therapeutic use of these antiviral peptide compounds.
DRAVP02868	AKTKPRQQ	8	Sequence 3 from Patent US 5447915 A	Synthetic construct	HIV	Granted Patent	US 5447915 A	1995-09-05	CA 2077088 A1##WO 1991/013088 A1##US 5115098 A##EP 0517792 A1##JP H05503535 A##US 5447915 A	Terminally blocked antiviral peptides	No comments found in patent	This invention relates to antiviral peptide compounds and to methods of inhibiting infection of human cells by viruses. This invention pertains more specifically to peptides that are chemically blocked at the amino- and carboxy-termini. In particular the invention relates to peptides comprised of prolylalanine or prolylphenylalanine compounds that have antiviral activity. The invention is specifically directed to methods for preventing infection of human cells in vivo and in vitro with the human immunodeficiency virus HIV-1 and methods for treating human infected with this and other viruses. The invention also relates to the diagnostic and therapeutic use of these antiviral peptide compounds.
DRAVP02869	ASTTTNYT	8	Sequence 4 from Patent US 5447915 A	Synthetic construct	HIV	Granted Patent	US 5447915 A	1995-09-05	CA 2077088 A1##WO 1991/013088 A1##US 5115098 A##EP 0517792 A1##JP H05503535 A##US 5447915 A	Terminally blocked antiviral peptides	No comments found in patent	This invention relates to antiviral peptide compounds and to methods of inhibiting infection of human cells by viruses. This invention pertains more specifically to peptides that are chemically blocked at the amino- and carboxy-termini. In particular the invention relates to peptides comprised of prolylalanine or prolylphenylalanine compounds that have antiviral activity. The invention is specifically directed to methods for preventing infection of human cells in vivo and in vitro with the human immunodeficiency virus HIV-1 and methods for treating human infected with this and other viruses. The invention also relates to the diagnostic and therapeutic use of these antiviral peptide compounds.
DRAVP02870	ACYCRIPACIAGERRYGTCIYQGRLWAFCC	30	Sequence 5 from Patent US 5447915 A	Synthetic construct	HIV	Granted Patent	US 5447915 A	1995-09-05	CA 2077088 A1##WO 1991/013088 A1##US 5115098 A##EP 0517792 A1##JP H05503535 A##US 5447915 A	Terminally blocked antiviral peptides	No comments found in patent	This invention relates to antiviral peptide compounds and to methods of inhibiting infection of human cells by viruses. This invention pertains more specifically to peptides that are chemically blocked at the amino- and carboxy-termini. In particular the invention relates to peptides comprised of prolylalanine or prolylphenylalanine compounds that have antiviral activity. The invention is specifically directed to methods for preventing infection of human cells in vivo and in vitro with the human immunodeficiency virus HIV-1 and methods for treating human infected with this and other viruses. The invention also relates to the diagnostic and therapeutic use of these antiviral peptide compounds.
DRAVP02871	DWLKAFYDKVAEKLKEAF	18	Sequence 6 from Patent US 5447915 A	Synthetic construct	HIV	Granted Patent	US 5447915 A	1995-09-05	CA 2077088 A1##WO 1991/013088 A1##US 5115098 A##EP 0517792 A1##JP H05503535 A##US 5447915 A	Terminally blocked antiviral peptides	No comments found in patent	This invention relates to antiviral peptide compounds and to methods of inhibiting infection of human cells by viruses. This invention pertains more specifically to peptides that are chemically blocked at the amino- and carboxy-termini. In particular the invention relates to peptides comprised of prolylalanine or prolylphenylalanine compounds that have antiviral activity. The invention is specifically directed to methods for preventing infection of human cells in vivo and in vitro with the human immunodeficiency virus HIV-1 and methods for treating human infected with this and other viruses. The invention also relates to the diagnostic and therapeutic use of these antiviral peptide compounds.
DRAVP02872	KWLDAFYKDVAKELEKAF	18	Sequence 7 from Patent US 5447915 A	Synthetic construct	HIV	Granted Patent	US 5447915 A	1995-09-05	CA 2077088 A1##WO 1991/013088 A1##US 5115098 A##EP 0517792 A1##JP H05503535 A##US 5447915 A	Terminally blocked antiviral peptides	No comments found in patent	This invention relates to antiviral peptide compounds and to methods of inhibiting infection of human cells by viruses. This invention pertains more specifically to peptides that are chemically blocked at the amino- and carboxy-termini. In particular the invention relates to peptides comprised of prolylalanine or prolylphenylalanine compounds that have antiviral activity. The invention is specifically directed to methods for preventing infection of human cells in vivo and in vitro with the human immunodeficiency virus HIV-1 and methods for treating human infected with this and other viruses. The invention also relates to the diagnostic and therapeutic use of these antiviral peptide compounds.
DRAVP02873	IKILGNQGSTLTKGPYSK	18	Sequence 8 from Patent US 5447915 A	Synthetic construct	HIV	Granted Patent	US 5447915 A	1995-09-05	CA 2077088 A1##WO 1991/013088 A1##US 5115098 A##EP 0517792 A1##JP H05503535 A##US 5447915 A	Terminally blocked antiviral peptides	No comments found in patent	This invention relates to antiviral peptide compounds and to methods of inhibiting infection of human cells by viruses. This invention pertains more specifically to peptides that are chemically blocked at the amino- and carboxy-termini. In particular the invention relates to peptides comprised of prolylalanine or prolylphenylalanine compounds that have antiviral activity. The invention is specifically directed to methods for preventing infection of human cells in vivo and in vitro with the human immunodeficiency virus HIV-1 and methods for treating human infected with this and other viruses. The invention also relates to the diagnostic and therapeutic use of these antiviral peptide compounds.
DRAVP02874	LKIEDSDTYICEVEDQKEE	19	Sequence 9 from Patent US 5447915 A	Synthetic construct	HIV	Granted Patent	US 5447915 A	1995-09-05	CA 2077088 A1##WO 1991/013088 A1##US 5115098 A##EP 0517792 A1##JP H05503535 A##US 5447915 A	Terminally blocked antiviral peptides	No comments found in patent	This invention relates to antiviral peptide compounds and to methods of inhibiting infection of human cells by viruses. This invention pertains more specifically to peptides that are chemically blocked at the amino- and carboxy-termini. In particular the invention relates to peptides comprised of prolylalanine or prolylphenylalanine compounds that have antiviral activity. The invention is specifically directed to methods for preventing infection of human cells in vivo and in vitro with the human immunodeficiency virus HIV-1 and methods for treating human infected with this and other viruses. The invention also relates to the diagnostic and therapeutic use of these antiviral peptide compounds.
DRAVP02875	TYICEVEDQKEE	12	Sequence 10 from Patent US 5447915 A	Synthetic construct	HIV	Granted Patent	US 5447915 A	1995-09-05	CA 2077088 A1##WO 1991/013088 A1##US 5115098 A##EP 0517792 A1##JP H05503535 A##US 5447915 A	Terminally blocked antiviral peptides	No comments found in patent	This invention relates to antiviral peptide compounds and to methods of inhibiting infection of human cells by viruses. This invention pertains more specifically to peptides that are chemically blocked at the amino- and carboxy-termini. In particular the invention relates to peptides comprised of prolylalanine or prolylphenylalanine compounds that have antiviral activity. The invention is specifically directed to methods for preventing infection of human cells in vivo and in vitro with the human immunodeficiency virus HIV-1 and methods for treating human infected with this and other viruses. The invention also relates to the diagnostic and therapeutic use of these antiviral peptide compounds.
DRAVP02876	XPXLX	5	Sequence 11 from Patent US 5447915 A	Synthetic construct	HIV	Granted Patent	US 5447915 A	1995-09-05	CA 2077088 A1##WO 1991/013088 A1##US 5115098 A##EP 0517792 A1##JP H05503535 A##US 5447915 A	Terminally blocked antiviral peptides	No comments found in patent	This invention relates to antiviral peptide compounds and to methods of inhibiting infection of human cells by viruses. This invention pertains more specifically to peptides that are chemically blocked at the amino- and carboxy-termini. In particular the invention relates to peptides comprised of prolylalanine or prolylphenylalanine compounds that have antiviral activity. The invention is specifically directed to methods for preventing infection of human cells in vivo and in vitro with the human immunodeficiency virus HIV-1 and methods for treating human infected with this and other viruses. The invention also relates to the diagnostic and therapeutic use of these antiviral peptide compounds.
DRAVP02877	WNASWSNKSLEQIWNNMTWMEWDREINNYTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	64	Sequence 1 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02878	YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWF	36	Sequence 2 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02879	MTWMEWDREINNYTSLIHSLIEESQNQQEKNEQELL	36	Sequence 3 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02880	WMEWDREINNYTSLIHSLIEESQNQQEKNEQELLEL	36	Sequence 4 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02881	TTWEAWDRAIAEYAARIEALIRAAQEQQEKNEAALREL	38	Sequence 5 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide shows antiviral activity against HIV-IIIB(IC50<0.10 ¦Ìg/ml) and HIV-Res(IC50<0.10 ¦Ìg/ml).	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02882	TTWEAWDRAIAEYAARIEALIRALQEQQEKNEAALREL	38	Sequence 6 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide shows antiviral activity against HIV-IIIB(IC50<0.10 ¦Ìg/ml) and HIV-Res(IC50>0.10 ¦Ìg/ml).	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02883	TTWEAWDRAIAEYAARIEALIRAAQEQQEKLEAALREL	38	Sequence 7 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide shows antiviral activity against HIV-IIIB(IC50<0.10 ¦Ìg/ml) and HIV-Res(IC50>0.10 ¦Ìg/ml).	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02884	TTWEAWDRAIAEYAARIEALLRAAQEQQEKNEAALREL	38	Sequence 8 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide shows antiviral activity against HIV-IIIB(IC50<0.10 ¦Ìg/ml).	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02885	TTWEAWDRAIAEYAARIEALLRALQEQQEKNEAALREL	38	Sequence 9 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide shows antiviral activity against HIV-IIIB(IC50<0.10 ¦Ìg/ml) and HIV-Res(IC50<0.10 ¦Ìg/ml).	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02886	TTWEAWDRAIAEYAARIEALLRAAQEQQEKLEAALREL	38	Sequence 10 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide shows antiviral activity against HIV-IIIB(IC50<0.10 ¦Ìg/ml) and HIV-Res(IC50<0.10 ¦Ìg/ml).	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02887	TTWEAWDRAIAEYAARIEALIRALQEQQEKLEAALREL	38	Sequence 11 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02888	TTWEAWDRAIAEYAARIEALIRAIQEQQEKLEAALREL	38	Sequence 12 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02889	TTWEAWDRAIAEYAARIEALIRALQEQQEKIEAALREL	38	Sequence 13 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02890	TTWEAWDRAIAEYAARIEALLRAIQEQQEKNEAALREL	38	Sequence 14 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02891	TTWEAWDRAIAEYAARIEALLRAAQEQQEKIEAALREL	38	Sequence 15 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02892	TTWEAWDRAIAE	12	Sequence 17 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with acetyl N-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02893	YAARIEALLRALQE	14	Sequence 18 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02894	QQEKNEAALRE	11	Sequence 19 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02895	QQEKNEAALREL	12	Sequence 20 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with amide C-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02896	TTWEAWDRAIA	11	Sequence 21 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with acetyl N-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02897	EYAARIEALLRALQE	15	Sequence 22 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02898	TTWEAWDRAI	10	Sequence 23 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with acetyl N-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02899	AEYAARIEALLRALQE	16	Sequence 24 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02900	TTWEAWDRA	9	Sequence 25 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with acetyl N-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02901	IAEYAARIEALLRALQE	17	Sequence 26 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02902	TTWEAWDR	8	Sequence 27 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with acetyl N-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02903	AIAEYAARIEALLRALQE	18	Sequence 28 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02904	TTWEAWDRAIAEYAARIEAL	20	Sequence 29 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with acetyl N-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02905	LRALQEQQEKNEAALRE	17	Sequence 30 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02906	LRALQEQQEKNEAALREL	18	Sequence 31 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with amide C-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02907	TTWEAWDRAIAEYAARIE	18	Sequence 32 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with acetyl N-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02908	ALLRALQEQQEKNEAALRE	19	Sequence 33 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02909	ALLRALQEQQEKNEAALREL	20	Sequence 34 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with amide C-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02910	YAARIEALLRALQEQQEKNEAALREL	26	Sequence 35 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02911	EYAARIEALLRALQEQQEKNEAALREL	27	Sequence 36 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02912	AEYAARIEALLRALQEQQEKNEAALREL	28	Sequence 37 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02913	IAEYAARIEALLRALQEQQEKNEAALREL	29	Sequence 38 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02914	AIAEYAARIEALLRALQEQQEKNEAALREL	30	Sequence 39 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02915	TTWEAWDRAIAEYAARIEALLRALQE	26	Sequence 40 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02916	YAARIEALLRAAQE	14	Sequence 41 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02917	QQEKLEAALRE	11	Sequence 42 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02918	QQEKLEAALREL	12	Sequence 43 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with amide C-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02919	EYAARIEALLRAAQE	15	Sequence 44 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02920	AEYAARIEALLRAAQE	16	Sequence 45 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02921	IAEYAARIEALLRAAQE	17	Sequence 46 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02922	AIAEYAARIEALLRAAQE	18	Sequence 47 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02923	LRAAQEQQEKLEAALRE	17	Sequence 48 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02924	LRAALQEQQEKLEAALREL	19	Sequence 49 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with amide C-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02925	ALLRAAQEQQEKLEAALRE	19	Sequence 50 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02926	ALLRAAQEQQEKLEAALREL	20	Sequence 51 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	The peptide was modified with amide C-terminus.	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02927	YAARIEALLRAAQEQQEKLEAALREL	26	Sequence 52 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02928	EYAARIEALLRAAQEQQEKLEAALREL	27	Sequence 53 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02929	AEYAARIEALLRAAQEQQEKLEAALREL	28	Sequence 54 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02930	IAEYAARIEALLRAAQEQQEKLEAALREL	29	Sequence 55 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02931	AIAEYAARIEALLRAAQEQQEKLEAALREL	30	Sequence 56 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02932	TTWEAWDRAIAEYAARIEALLRALQEQQEKNEAALRE	37	Sequence 57 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02933	AARIEALLRALQEQQEKNEAALRE	24	Sequence 58 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02934	RIEALLRALQEQQEKNEAALRE	22	Sequence 59 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02935	QEQQEKNEAALREL	14	Sequence 60 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02936	LQEQQEKNEAALREL	15	Sequence 61 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02937	EQQEKNEAALREL	13	Sequence 62 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02938	TTWEAWDRAIAEYAARIEALLRALQ	25	Sequence 63 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02939	TTWEAWDRAIAEYAARIEALLRAL	24	Sequence 64 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02940	TTWEAWDRAIAEYAARIEALLR	22	Sequence 65 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02941	TTWEAWDRAIAEYAARIEALL	21	Sequence 66 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02942	TTWEAWDRAIAEYAARIEA	19	Sequence 67 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02943	TTWEAWDRAIAEYAARI	17	Sequence 68 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02944	TTWEAWDRAIAEYAAR	16	Sequence 69 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02945	TTWEAWDRAIAEYAA	15	Sequence 70 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02946	TTWEAWDRAIAEYA	14	Sequence 71 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02947	TYWEAWDRAIAEY	13	Sequence 72 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02948	EL	2	Sequence 73 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02949	AARIEALLRALQE	13	Sequence 74 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02950	ARIEALLRALQE	12	Sequence 75 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02951	RIEALLRALQE	11	Sequence 76 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02952	EALLRALQE	9	Sequence 77 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02953	WQEWEQKITALLEQAQIQQEKNEYELQKLDKWASLWEWF	39	Sequence 78 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02954	YTSLIHSLIEESQNQQEKNEQELLELDKWASLWNWFNIT	39	Sequence 79 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02955	YQEWERKVDFLEENITALLEEAQIQQEKNMYELQKL	36	Sequence 80 from Patent US 20100261876 A1	Synthetic construct	HIV	Patent Application	US 2010/0261876 A1	2010-10-14	CA 2700354 A1##WO 2009/042194 A2##WO 2009/042194 A3##MX 2010003179 A##EP 2201028 A2##KR 20100080812 A##US 2010/0261876 A1##CN 101874038 A##JP 2010540528 A##BR PI0817697 A2	Novel Methods of Synthesis for Therapeutic Antiviral Peptides	No comments found in patent	"Provided herein are methods for synthesis of peptides. In particular, provided herein are methods of synthesis for therapeutic antiviral peptides."
DRAVP02956	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQLLGI	59	Sequence 1 from Patent US 20040091855	Human immunodeficiency virus	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02957	NNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	38	Sequence 2 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02958	GSTMGARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLT	43	Sequence 3 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02959	GSTMGARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARI	54	Sequence 4 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02960	GARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLL	36	Sequence 5 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02961	GARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQL	38	Sequence 6 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02962	GARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTV	40	Sequence 7 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02963	GARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARI	50	Sequence 8 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02964	ARSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQ	36	Sequence 9 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02965	RSMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQL	36	Sequence 10 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02966	SMTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLT	36	Sequence 11 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02967	MTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLT	35	Sequence 12 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02968	MTLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTV	36	Sequence 13 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02969	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLT	34	Sequence 14 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02970	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTV	35	Sequence 15 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02971	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVW	36	Sequence 16 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02972	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWG	37	Sequence 17 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02973	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGI	38	Sequence 18 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02974	TLTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQAR	44	Sequence 19 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02975	LTVQARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWG	36	Sequence 20 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02976	QARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARIL	42	Sequence 21 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02977	QARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERY	47	Sequence 22 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02978	QARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLK	49	Sequence 23 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=4.69 ¦Ìg/ml, IC90=23.24 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02979	QARQLLSGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	51	Sequence 24 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=3.73 ¦Ìg/ml, IC90=12.301 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02980	SGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARIL	36	Sequence 25 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02981	SGIVQQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	45	Sequence 26 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02982	QQQNNLLRAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	41	Sequence 27 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=4.69 ¦Ìg/ml, IC90=23.24 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02983	RAIEAQQHLLQLTVWGIKQLQARILAVERYLKDQ	34	Sequence 28 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02984	QQQNNLLRAIEAQQHLLQLTAWGIKQLQARILAVERYLKDQ	41	Sequence 29 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=2.81 ¦Ìg/ml, IC90=5.86 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02985	QQQNNLLRAIEAQQHLLQLTVAGIKQLQARILAVERYLKDQ	41	Sequence 30 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=0.37 ¦Ìg/ml, IC90=1.00 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02986	QARQLLSGIVQQQNNLLRAIEAQQHLLQLTVFGIRQLQARILAVERYLK	49	Sequence 31 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=0.93 ¦Ìg/ml, IC90=3.06 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02987	QARQLLSGIVQQQNNLLRAIEAQQHALQATVWGIKQLQARILAVERYLK	49	Sequence 32 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=0.59 ¦Ìg/ml, IC90=1.90 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02988	WMEWDREINNYTSLIHSLIEESQNQQEKNEQELLEL	36	Sequence 33 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02989	QARQLLSGIVQQQNNLLRAIEAQQHALQATVWGIKQLQARILAVERYLKDQ	51	Sequence 34 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=0.19 ¦Ìg/ml, IC90=0.62 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02990	QARQLVSGLVQQQNNILRALEATQHAVQALVWGVKQLQARVLALERYIK	49	Sequence 35 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=0.14 ¦Ìg/ml, IC90=0.69 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02991	QIRQLLSGIVQQQNNLLRAIEAIQHALQAIVWGIKQLQARILAVERYLK	49	Sequence 36 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=0.73 ¦Ìg/ml, IC90=3.03 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02992	QARQLVSGLVQQQNNILRALEATQHAVQALVWGVRQLQARVLALERYIK	49	Sequence 37 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	The peptide shows antiviral activity against HIV IIIB.(IC50<0.78 ¦Ìg/ml)	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02993	QARQLLSGIVQQQNNLLRAIEATQHAVQALVWGVKQLQARVLALERYIKDQ	51	Sequence 38 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=0.18 ¦Ìg/ml, IC90=0.88 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02994	QARQLVSGLVQQQNNILRALEAQQHALQATVWGIKQLQARVLALERYIKDQ	51	Sequence 39 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=0.26 ¦Ìg/ml, IC90=1.20 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02995	QARQLLSGIVQQQNNLLRAIEAQQHALQATVWGVKQLQARILAVERYLKDQ	51	Sequence 40 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=0.41 ¦Ìg/ml, IC90=1.84 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02996	QARQLVSGLVQQQNNILRALEATQHLVQLLVWGVKQLQARVLALERYIK	49	Sequence 41 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=3.892 ¦Ìg/ml, IC90=14.53 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02997	QIRQLLSGIVQQQNNLLRAIEAIQHLLQLIVWGIKQLQARILAVERYLK	49	Sequence 42 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=13.605 ¦Ìg/ml, IC90=33.56 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02998	QQQNNLLRAIEAQQHLLQLTVFGIKQLQARILAVERYLKDQ	41	Sequence 43 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	"The peptide shows antiviral activity against HIV IIIB.(IC50=1.34 ¦Ìg/ml, IC90=3.81 ¦Ìg/ml)"	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP02999	QQQNNLLRAIEAQQHLLQLTVWGIAQLQARILAVERYLKDQ	41	Sequence 44 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP03000	QQQNNLLRAIEAQQHLLQLTVWGIKQLAARILAVERYLKDQ	41	Sequence 45 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP03001	QQQNNLLRAIEAQQHALQLTVWGIKQLQARILAVERYLKDQ	41	Sequence 46 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	No comments found in patent	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP03002	QARQLLSGIVQQQNNLLRAIEAQQHLLQATVWGIKQLQARILAVERYLKDQ	51	Sequence 47 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	The peptide shows antiviral activity against HIV IIIB.(IC50=0.61 ¦Ìg/ml)	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP03003	QQQNNLLRAIEAQQHLLQATVWGIKQLQARILAVERYLKDQ	41	Sequence 48 from Patent US 20040091855	Synthetic construct	HIV	Patent Application	US 2004/0091855 A1	2004-05-13	US 2004/0091855 A1	"Method for production of antivirals by use of HIV-derived HR1 peptides, and trimers formed therefrom"	The peptide shows antiviral activity against HIV IIIB.(IC50=0.89 ¦Ìg/ml)	"Provided is a method for identifying or producing a molecule having antiviral activity against HIV. More particularly, provided is a method for identifying or producing a molecule that can inhibit the binding between HR1 and HR2 regions of HIV gp41, wherein complex formation is observed in vitro between a trimer with HR2 peptide in the presence of the molecule, and detected in vitro is the ability of the molecule to inhibit complex formation as an indicator of the antiviral activity of the molecule. The trimer is comprised of synthetic peptide comprising an amino acid sequence derived from the HR1 region of HIV-1 gp41 and further comprising one or more amino acid substitutions in a hydrophobic domain of the HR1 region of HIV which enable the synthetic peptide to self-assemble in solution into trimers."
DRAVP03004	RRKKAAVALLPAVLLALLAP	20	Sequence 1 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses.The peptide shows antiviral activity against HSV by blocking virus entry(IC50=15-26 ¦ÌM)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03005	RRKKAAVALLAVLLALLAPP	20	Sequence 3 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03006	RRKKPAVLLALLA	13	Sequence 4 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03007	KLALKLALKALKAALKLA	18	Sequence 5 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses.The peptide shows antiviral activity against HSV by blocking virus entry(IC50=11 ¦ÌM)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03008	RQIKIWFPNRRMKWKKPGYAGAVVNDL	27	Sequence 7 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses.The peptide shows antiviral activity against HSV by blocking virus entry(IC50=9-12 ¦ÌM)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03009	RQIKIWFPNRRMKWKK	16	Sequence 8 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses.The peptide shows antiviral activity against HSV by blocking virus entry(IC50=7 ¦ÌM)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03010	RQIKIFFPNRRMKFKK	16	Sequence 9 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses.The peptide shows antiviral activity against HSV by blocking virus entry(IC50=40 ¦ÌM)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03011	YGRKKRRQRRRPGYAGAVVNDL	22	Sequence 10 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses.The peptide shows antiviral activity against HSV by blocking virus entry(IC50=26 ¦ÌM)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03012	YGRKKRRQRRRPGDVYANGLVA	22	Sequence 11 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses.The peptide shows antiviral activity against HSV by blocking virus entry(IC50=67 ¦ÌM)."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03013	GWTLNSAGYLLGKINLKALAALAKKIL	27	Sequence 12 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03014	DPKGDPKGVTVTVTVTVTGKGDPKPD	26	Sequence 13 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03015	RRKK	4	Sequence 16 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03016	RRKKLAALPLVLAAPLAVLA	20	Sequence 17 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03017	RRKKAAVALLP	11	Sequence 18 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03018	RRKKAVAVAVPAVLLALLAP	20	Sequence 19 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03019	RRKKPAVLLA	10	Sequence 20 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03020	RRKKPAVLLALLALLA	16	Sequence 22 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03021	RRKKALLPAVLLALLAP	17	Sequence 23 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03022	RRKKPAVLLALLAP	14	Sequence 24 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03023	RRKKLLALLAP	11	Sequence 25 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03024	RRKKLLAP	8	Sequence 26 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03025	RRKKAAVALLPAVLLAL	17	Sequence 27 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03026	RRKKAAVAVVPAVL	14	Sequence 28 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03027	RRKKAAVAVVP	11	Sequence 29 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03028	RRKKAAVA	8	Sequence 30 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03029	PGYAGAVVNDL	11	Sequence 31 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03030	PGDVYANGLVA	11	Sequence 32 from Patent US 20050130884	Synthetic construct	HSV	Patent Application	US 2005/0130884 A1	2005-06-16	WO 2001/057072 A2##CA 2399676 A1##AU 2001/036700 A##WO 2001/057072 A3##EP 1272510 A2##JP 2003522185 A##US 2005/0130884 A1##AU 784264 B2##EP 1272510 B1##AT 374208 T##DE 60130641 D1##ES 2293977 T3##US 7	Pharmacologically active antiviral peptides and methods of their use	"The peptide shows antiviral activity against a wide range of enveloped and non-enveloped viruses. Examples of such enveloped viruses include, but are not limited to, human immunodeficiency virus (HIV), vesiculovirus (VSV), herpes simplex viruses (HSV-1 and HSV-2), and other herpes viruses, for example, varicella-zoster virus (VZV), EBV, equine herpes virus (EHV), and human cytomegalovirus (HCMV). Examples of non-enveloped viruses include, but are not limited to, human papilloma virus (HPV) and adenoviruses."	"This invention relates to peptides having antiviral properties. The antiviral peptides comprise membrane transiting peptides, and active fragments and derivatives of such peptides. The antiviral peptides exhibit activity against a broad spectrum of viruses, including enveloped and nonenveloped viruses, and are used in pharmaceutical compositions to prevent and/or treat viral infections."
DRAVP03031	SWLRDVWDWICTVL	14	Sequence 2 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV2), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses. "	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03032	SWLRDVWDWVCTIL	14	Sequence 3 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV3), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03033	SWLRDIWEWVLSIL	14	Sequence 4 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV4), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03034	SWLRIIWDWVCSWC	14	Sequence 5 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV5), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03035	SWLRTIWDWVCSVC	14	Sequence 6 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV6), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03036	SWLHDIWDWVCIVC	14	Sequence 7 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV7), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03037	SWLWDVWDWVLHVL	14	Sequence 8 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV8), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03038	SWLYDIVNWVCTVC	14	Sequence 9 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV9), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03039	SWLRDIWDWVCTVC	14	Sequence 10 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV10), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03040	SWLRDIWDWICEVL	14	Sequence 11 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV11), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03041	LRDIWDWICEVLSDFKTWLKA	21	Sequence 12 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV12), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03042	WLRDVWDWICTVLTDFKTWLQSKL	24	Sequence 13 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV13), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03043	WLRDVWDWVCTILTDFKNWLTSKL	24	Sequence 14 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV14), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03044	WLRDIWEWVLSILTDFKNWLSAKL	24	Sequence 15 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV15), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03045	WLRIIWDWVCSVVSDFKTWLSAKI	24	Sequence 16 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV16), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03046	WLRTIWDWVCSVLADFKAWLSAKI	24	Sequence 17 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV17), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03047	WLHDIWDWVCIVLSDFKTWLSAKI	24	Sequence 18 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV18), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03048	WLWDVWDWVLHVLSDFKTCLKAKF	24	Sequence 19 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV19), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03049	WLYDIVNWVCTVLADFKLWLGAKI	24	Sequence 20 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV20), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03050	WLRDIWDWVCTVLSDFRVWLKSKL	24	Sequence 21 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV21), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03051	SWLRDVWDWICTVLTDFKTWLQSKL	25	Sequence 22 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV22), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03052	SWLRDVWDWVCTILTDFKNWLTSKL	25	Sequence 23 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV23), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03053	SWLRDIWEWVLSILTDFKNWLSAKL	25	Sequence 24 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV24), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03054	SWLRIIWDWVCSWSDFKTWLSAKI	24	Sequence 25 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV25), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03055	SWLRTIWDWVCSVLADFKAWLSAKI	25	Sequence 26 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV26), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03056	SWLHDIWDWVCIVLSDFKTWLSAKI	25	Sequence 27 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV27), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03057	SWLWDVWDWVLHVLSDFKTCLKAKF	25	Sequence 28 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV28), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03058	SWLYDIVNWVCTVLADFKLWLGAKI	25	Sequence 29 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV29), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03059	SWLRDIWDWVCTVLSDFRVWLKSKL	25	Sequence 30 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV30), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03060	SGSLRDIWDWICEVLSDFKTWLKA	24	Sequence 31 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV31), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03061	SGSWLRDVWDWICTVLTDFKTWLQSKL	27	Sequence 32 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV32), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03062	SGSWLRDVWDWVCTILTDFKNWLTSKL	27	Sequence 33 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV33), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03063	SGSWLRDIWEWVLSILTDFKNWLSAKL	27	Sequence 34 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV34), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03064	SGSWLRIIWDWVCSWSDFKTWLSAKI	26	Sequence 35 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV35), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03065	SGSWLRTIWDWVCSVLADFKAWLSAKI	27	Sequence 36 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV36), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03066	SGSWLHDIWDWVCIVLSDFKTWLSAKI	27	Sequence 37 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV37), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03067	SGSWLWDVWDWVLHVLSDFKTCLKAKF	27	Sequence 38 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV38), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03068	SGSWLYDIVNWVCTVLADFKLWLGAKI	27	Sequence 39 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV39), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03069	SGSWLRDIWDWVCTVLSDFRVWLKSKL	27	Sequence 40 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV40), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03070	GSWLRDVWDWICTVLTDFKTWLQSKL	26	Sequence 41 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV41), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03071	GSWLRDVWDWVCTILTDFKNWLTSKL	26	Sequence 42 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV42), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03072	GSWLRDIWEWVLSILTDFKNWLSAKL	26	Sequence 43 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV43), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03073	GSWLRIIWDWVCSWSDFKTWLSAKI	25	Sequence 44 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV44), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03074	GSWLRTIWDWVCSVLADFKAWLSAKI	26	Sequence 45 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV45), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03075	GSWLHDIWDWVCIVLSDFKTWLSAKI	26	Sequence 46 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV46), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03076	GSWLWDVWDWVLHVLSDFKTCLKAKF	26	Sequence 47 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV47), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03077	GSWLYDIVNWVCTVLADFKLWLGAKI	26	Sequence 48 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV48), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03078	GSWLRDIWDWVCTVLSDFRVWLKSKL	26	Sequence 49 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV49), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03079	SWLRDVWDWICTVLT	15	Sequence 50 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV50), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03080	SWLRDVWDWVCTILT	15	Sequence 51 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV51), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03081	SWLRDIWEWVLSILT	15	Sequence 52 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV52), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03082	SWLRIIWDWVCSWSD	15	Sequence 53 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV53), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03083	SWLRTIWDWVCSVLA	15	Sequence 54 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV54), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03084	SWLHDIWDWVCIVLS	15	Sequence 55 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV55), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03085	SWLWDVWDWVLHVLS	15	Sequence 56 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV56), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03086	SWLYDIVNWVCTVLA	15	Sequence 57 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV57), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03087	SWLRDIWDWVCTVLS	15	Sequence 58 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV58), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03088	SWLRDVWDWICTVLTD	16	Sequence 59 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV59), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03089	SWLRDVWDWVCTILTD	16	Sequence 60 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV60), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03090	SWLRDIWEWVLSILTD	16	Sequence 61 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV61), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03091	SWLRIIWDWVCSWSDF	16	Sequence 62 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV62), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03092	SWLRTIWDWVCSVLAD	16	Sequence 63 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV63), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03093	SWLHDIWDWVCIVLSD	16	Sequence 64 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV64), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03094	SWLWDVWDWVLHVLSD	16	Sequence 65 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV65), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03095	SWLYDIVNWVCTVLAD	16	Sequence 66 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV66), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03096	SWLRDIWDWVCTVLSD	16	Sequence 67 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV67), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03097	SWLRDVWDWICTVLTDF	17	Sequence 68 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV68), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03098	SWLRDVWDWVCTILTDF	17	Sequence 69 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV69), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03099	SWLRDIWEWVLSILTDF	17	Sequence 70 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV70), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03100	SWLRIIWDWVCSWSDFK	17	Sequence 71 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV71), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03101	SWLRTIWDWVCSVLADF	17	Sequence 72 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV72), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03102	SWLHDIWDWVCIVLSDF	17	Sequence 73 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV73), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03103	SWLWDVWDWVLHVLSDF	17	Sequence 74 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV74), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03104	SWLYDIVNWVCTVLADF	17	Sequence 75 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV75), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03105	SWLRDIWDWVCTVLSDF	17	Sequence 76 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV76), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03106	SGSWLRDVWDWICTVLTDFKTWLQSKLDYK	30	Sequence 77 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV77), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03107	QDVLKEVKAAASKVKANLLSVEE	23	Sequence 79 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV78), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03108	DVRCHARKAVAHINSVWKD	19	Sequence 80 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV79), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03109	IEQGMMLAEQFKQKALGLLQTASRHAEV	28	Sequence 81 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV80), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03110	LRDVWDWICTVLTDFKT	17	Sequence 83 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV81), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03111	LRDVWDWICT	10	Sequence 84 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV82), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03112	DVWDWICTVLTD	12	Sequence 85 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV83), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03113	SWLRDVWDWIC	11	Sequence 86 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV84), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03114	LCLAGRGLQEAEGLLLELLSEHHPLLDV	28	Sequence 87 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV85), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03115	ELGFQPGLKVAQHLAYPVPDVP	22	Sequence 88 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV86), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03116	SGSWLRDVWDWICTVLTDFKTWLQSKLDYKD	31	Sequence 89 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV87), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03117	SGSWLRDDWDWECTVLTDDKTWLQSKLDYKD	31	Sequence 90 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV88), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03118	SGSWLRDDWDWECTVLTDDKTWLQSKL	27	Sequence 91 from Patent US 20090105151	Hepatitis C virus	HCV	Patent Application	US 2009/0105151 A1	2009-04-23	WO 2009/014615 A2##US 2009/0105151 A1##WO 2009/014615 A3##US 8728793 B2	Amphipathic Alpha-Helical Peptide Compositions as Antiviral Agents	"The peptide effects viral envelope disruption, which serves to inhibit viral infection, inhibit viral replication, reduce viral load and reduce infectivity. And It may be used to treat disease caused by one or more of the following viruses: poxvirus, baculovirus, paramyxoviruses, arenaviruses, herpesviruses (e.g., HSV (e.g., HSV1, HSV89), CMV, EBV, etc.), orthomyxoviruses, bunya viruses, coronaviruses, retroviruses (e.g., HIV), togaviruses, flaviviruses and hepadnaviruses."	"The invention features methods and compositions that exploit the ability of amphipathic alpha-helical (AH) peptides to cause disruption of lipid-containing vesicles, such as enveloped viruses, in a size-dependent manner."
DRAVP03119	RLLLRLLLGY	10	Sequence 3 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03120	RVLLRLLLGY	10	Sequence 4 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03121	RILLRLLLGY	10	Sequence 5 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03122	RLVLRLLLGY	10	Sequence 6 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03123	RLILRLLLGY	10	Sequence 7 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03124	RLLVRLLLGY	10	Sequence 8 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03125	RLLIRLLLGY	10	Sequence 9 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03126	RLLLRVLLGY	10	Sequence 10 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03127	RLLLRILLGY	10	Sequence 11 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03128	RLLLRLVLGY	10	Sequence 12 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03129	RLLLRLILGY	10	Sequence 13 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03130	RLLLRLLVGY	10	Sequence 14 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03131	RLLLRLLIGY	10	Sequence 15 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03132	RWLLRLLLGY	10	Sequence 16 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03133	RLWLRLLLGY	10	Sequence 17 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03134	RLLWRLLLGY	10	Sequence 18 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03135	RLLLRWLLGY	10	Sequence 19 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03136	RLLLRLWLGY	10	Sequence 20 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03137	RLLLRLLWGY	10	Sequence 21 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03138	RYLLRLLLGY	10	Sequence 22 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03139	RLYLRLLLGY	10	Sequence 23 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03140	RLLYRLLLGY	10	Sequence 24 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03141	RLLLRYLLGY	10	Sequence 25 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03142	RLLLRLYLGY	10	Sequence 26 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03143	RLLLRLLYGY	10	Sequence 27 from Patent US 20090215699	Synthetic construct	HIV	Patent Application	US 2009/0215699 A1	2009-08-27	CA 2592888 A1##WO 2006/072579 A1##EP 1838333 A1##US 2009/0215699 A1	Pharmaceutically Active Antiviral Peptides	No cooments found in patent	"The inventive peptides were found to have strong antiviral activity against HIV in general and particularly strong drug-resistant HIV activity without exerting any toxic or antiproliferative effects on cells. Consequently, using of the inventive peptides improves the conventional HIV therapy with its toxic side effects."
DRAVP03144	RQARRNRRRRWR	12	Sequence 1 from Patent US 20090258815	Human immunodeficiency virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03145	RKKRRQRRR	9	Sequence 2 from Patent US 20090258815	Human immunodeficiency virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03146	PKKKRKV	7	Sequence 3 from Patent US 20090258815	Simian virus 40	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03147	RKKKRKV	7	Sequence 4 from Patent US 20090258815	Synthetic construct	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03148	YGRKKRRQRRR	11	Sequence 5 from Patent US 20090258815	Human immunodeficiency virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03149	LPPLERLTLD	10	Sequence 6 from Patent US 20090258815	Human immunodeficiency virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03150	LALKLAGLDI	10	Sequence 7 from Patent US 20090258815	Mus musculus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03151	LPPDLRLTLD	10	Sequence 8 from Patent US 20090258815	Human immunodeficiency virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03152	LSAQLYSSLSLD	12	Sequence 9 from Patent US 20090258815	Human T-cell lymphotropic	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03153	RQARRNRRRRWRLPPLERLTLD	22	Sequence 10 from Patent US 20090258815	Synthetic construct	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03154	LPPLERLTLDRQARRNRRRRWR	22	Sequence 11 from Patent US 20090258815	Synthetic construct	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03155	YGRKKRRQRRRLPPLERLTLD	21	Sequence 12 from Patent US 20090258815	Synthetic construct	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03156	RKKKRKVLALKAGLDI	16	Sequence 13 from Patent US 20090258815	Synthetic construct	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03157	RRMKWKK	7	Sequence 14 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03158	RVHPYQR	7	Sequence 15 from Patent US 20090258815	Mus musculus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03159	KRPACTLKPECVQQLLVCSQEAKK	24	Sequence 16 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03160	PKKKRKV	7	Sequence 17 from Patent US 20090258815	Simian virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03161	GKKRSKA	7	Sequence 18 from Patent US 20090258815	Saccharomyces cerevisiae	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03162	KAKRQR	6	Sequence 19 from Patent US 20090258815	avian reticuloendothelios	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03163	RGRRRRQR	8	Sequence 20 from Patent US 20090258815	Rattus sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03164	RKRRR	5	Sequence 21 from Patent US 20090258815	Rattus sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03165	PPVKRERTS	9	Sequence 22 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03166	PYLNKRKGKP	10	Sequence 23 from Patent US 20090258815	Saccharomyces cerevisiae	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03167	CYGSKNTGAKKRKIDDA	17	Sequence 24 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03168	KKKKRKREK	9	Sequence 25 from Patent US 20090258815	Drosophila sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03169	KKKRRSREK	9	Sequence 26 from Patent US 20090258815	Drosophila sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03170	KVTKRKHDNEGSGSKRPK	18	Sequence 27 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03171	KKKKKEEEGEGKKK	14	Sequence 28 from Patent US 20090258815	Rattus sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03172	PRPRKIPR	8	Sequence 29 from Patent US 20090258815	Borna disease virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03173	PPRIYPQLPSAPT	13	Sequence 30 from Patent US 20090258815	Borna disease virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03174	KDCVINKHHRNRCQYCRLQR	20	Sequence 31 from Patent US 20090258815	Mus musculus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03175	APKRKSGVSKC	11	Sequence 32 from Patent US 20090258815	Polyomavirus sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03176	RKKRRQRRR	9	Sequence 33 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03177	RQARRNRRRRWR	12	Sequence 34 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03178	MPKTRRRPRRSQRKRPPT	18	Sequence 35 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03179	KRPMNAFIVWSRDQRRK	17	Sequence 36 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03180	RPRRK	5	Sequence 37 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03181	KRPMNAFIVWAQAARRK	17	Sequence 38 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03182	PRRRK	5	Sequence 39 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03183	RKRR	4	Sequence 40 from Patent US 20090258815	Arabidopsis sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03184	PPRKKRTVV	9	Sequence 41 from Patent US 20090258815	Hepatitis C virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03185	YKRPCKRSFIRFI	13	Sequence 42 from Patent US 20090258815	epstein-barr virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03186	LKDVRKRKLGPGH	13	Sequence 43 from Patent US 20090258815	epstein-barr virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03187	KRPRP	5	Sequence 44 from Patent US 20090258815	adenovirus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03188	RKRKK	5	Sequence 45 from Patent US 20090258815	Saccharomyces cerevisiae	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03189	RRSMKRK	7	Sequence 46 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03190	PAKRARRGYK	10	Sequence 47 from Patent US 20090258815	canine parvovirus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03191	RKCLQAGMNLEARKTKK	17	Sequence 48 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03192	RRERNKMAAAKCRNRRR	17	Sequence 49 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03193	KRMRNRIAASKCRKRKL	17	Sequence 50 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03194	KKSKKGRQEALERLKKA	17	Sequence 51 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03195	RKEWLTNFMEDRRQRKL	17	Sequence 52 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03196	KKQTTLAFKPIKKGKKR	17	Sequence 53 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03197	RKRKKMPASQRSKRRKT	17	Sequence 54 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03198	RAIKRRPGLDFDDDGEGNSKFLR	23	Sequence 55 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03199	RIRKKLR	7	Sequence 56 from Patent US 20090258815	Mus musculus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03200	KRAAEDDEDDDVDTKKQK	18	Sequence 57 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03201	GRKRKKRT	8	Sequence 58 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03202	REKKEKEQKEKCA	13	Sequence 59 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03203	LEKKVKKKFDWCA	13	Sequence 60 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03204	RKRRTKK	7	Sequence 61 from Patent US 20090258815	Arabidopsis sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03205	SDKKVRSRLIECA	13	Sequence 62 from Patent US 20090258815	Thermoplasma acidophilum	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03206	LKRKLQR	7	Sequence 63 from Patent US 20090258815	avian neuroretina	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03207	RRKGKEK	7	Sequence 64 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03208	CKRKTTNADRRKA	13	Sequence 65 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03209	VNEAFETLKRC	11	Sequence 66 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03210	MPTEERVRKRKESNRESARRSRYRKAAHLK	30	Sequence 67 from Patent US 20090258815	Zea mays	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03211	KVNSRKRRKEVPGPNGATEED	21	Sequence 68 from Patent US 20090258815	Rattus sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03212	PRRGPR	6	Sequence 69 from Patent US 20090258815	Hepatitis C virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03213	PRGRRQPIPKARQP	14	Sequence 70 from Patent US 20090258815	Hepatitis C virus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03214	KRSAEGGNPPKPLKKLR	17	Sequence 71 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03215	EYLSRKGKLEL	11	Sequence 72 from Patent US 20090258815	Agrobacterium tumefaciens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03216	PKRPRDRHDGELGGRKRARG	20	Sequence 73 from Patent US 20090258815	Agrobacterium tumefaciens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03217	KRPAATKKAGQAKKKK	16	Sequence 74 from Patent US 20090258815	Xenopus sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03218	KRKKEMANKSAPEAKKKK	18	Sequence 75 from Patent US 20090258815	Gallus gallus	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03219	YNNQSSNFGPMKGGN	15	Sequence 76 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03220	PAAKRVKLD	9	Sequence 77 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03221	KRPAEDMEEEQAFKRSR	17	Sequence 78 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03222	MNKIPIKDLLNPG	13	Sequence 79 from Patent US 20090258815	Saccharomyces cerevisiae	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03223	PKKARED	7	Sequence 80 from Patent US 20090258815	Polyomavirus sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03224	VSRKRPR	7	Sequence 81 from Patent US 20090258815	Polyomavirus sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03225	APTKRKGS	8	Sequence 82 from Patent US 20090258815	Simian virus 40	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03226	PNKKKRK	7	Sequence 83 from Patent US 20090258815	Simian virus 40	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03227	EEDGPQKKKRRL	12	Sequence 84 from Patent US 20090258815	Polyomavirus sp.	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03228	PLLKKIKQ	8	Sequence 85 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03229	PPQKKIKS	8	Sequence 86 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03230	PQPKKKP	7	Sequence 87 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03231	SKRVAKRKL	9	Sequence 88 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03232	IKYFKKFPKD	10	Sequence 89 from Patent US 20090258815	Saccharomyces cerevisiae	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03233	KTRKHRG	7	Sequence 90 from Patent US 20090258815	Saccharomyces cerevisiae	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03234	KHRKHPG	7	Sequence 91 from Patent US 20090258815	Saccharomyces cerevisiae	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03235	PQSRKKLR	8	Sequence 92 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03236	KKEKKKSKK	9	Sequence 93 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03237	KRKKRRHR	8	Sequence 94 from Patent US 20090258815	Homo sapiens	Herpes viruse	Patent Application	US 2009/0258815 A1	2009-10-15	WO 2007/099993 A1##JP 2007230903 A##US 2009/0258815 A1##JP 4831410 B2##US 8138146 B2	Antiviral Peptide and Antiviral Agent	No cooments found in patent	"Disclosed is an antiviral agent comprising a non-naturally occurring, artificially synthesized peptide as the main ingredient. The antiviral agent comprises an antiviral peptide, wherein the antiviral peptide has at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear localization sequence (NLS)) or an amino acid sequence having a partial modification in the NLS and also having at least one unit of an amino acid sequence constituted by at least five contiguous amino acid residues (which is known as a nuclear export sequence (NES)) or an amino acid sequence having a partial modification in the NES."
DRAVP03238	EAQSQEVKNW MTETLLVQNA N	21	Sequence 2 from Patent US 20090281041	Homo sapiens	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	No cooments found in patent	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03239	AQEVKNWMTETLLVA	15	Sequence 3 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	No cooments found in patent	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03240	AQEVKXWMTXTLLVA	15	Sequence 4 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50=4.29 ¡À 0.62 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50>116 ¦ÌM).The 'X' at position 6 and 10 indicates (S)-a-2-(2'-pentenyl)alanine, X(6) and X(10) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03241	AQAVKXWMTXTLLVA	15	Sequence 5 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50=2.36 ¡À 0.33 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50=30.2 ¡À 4.32 ¦ÌM).The 'X' at position 6 and 10 indicates (S)-a-2-(2'-pentenyl)alanine, X(6) and X(10) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03242	AQEVKXWMTXTLLVAKKK	18	Sequence 6 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50=6.29 ¡À 0.54 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50=13.24 ¡À 0.5 ¦ÌM).The 'X' at position 6 and 10 indicates (S)-a-2-(2'-pentenyl)alanine, X(6) and X(10) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03243	AQKVEXWMTXTLLVA	15	Sequence 7 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50=5.15 ¡À 0.76 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50>112 ¦ÌM).The 'X' at position 6 and 10 indicates (S)-a-2-(2'-pentenyl)alanine, X(6) and X(10) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03244	AQAVKXWMTXTLLVENA	17	Sequence 8 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50=2.95 ¡À 0.33 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50>102 ¦ÌM).The 'X' at position 6 and 10 indicates (S)-a-2-(2'-pentenyl)alanine, X(6) and X(10) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03245	AQAVKXWMTXTLLKANAE	18	Sequence 9 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50=17.4 ¡À 0.90 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50>48 ¦ÌM).The 'X' at position 6 and 10 indicates (S)-a-2-(2'-pentenyl)alanine, X(6) and X(10) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03246	EQLVWXKMTXALAVT	15	Sequence 10 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50>56 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50>112 ¦ÌM).The 'X' at position 6 and 10 indicates (S)-a-2-(2'-pentenyl)alanine, X(6) and X(10) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03247	AQEVKNWMTE TLLVA	15	Sequence 11 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	No cooments found in patent	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03248	AQAVKNWMTXTLLXA	15	Sequence 12 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50=4.6 ¡À 0.40 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50=67.3 ¡À 4.4 ¦ÌM).The 'X' at position 10 and 14 indicates (S)-a-2-(2'-pentenyl)alanine, X(10) and X(14) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03249	AQAWKXWATXTLLVAE	16	Sequence 13 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50=3.7 ¡À 0.06 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50>106 ¦ÌM).The 'X' at position 6 and 10 indicates (S)-a-2-(2'-pentenyl)alanine, X(6) and X(10) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03250	AQAVKXWMEXTLKVAE	16	Sequence 14 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50>52.7 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50>105.4 ¦ÌM).The 'X' at position 6 and 10 indicates (S)-a-2-(2'-pentenyl)alanine, X(6) and X(10) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03251	AQAVKXWMTETLXVA	15	Sequence 15 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50=7.97 ¡À 1.03 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50>140.4 ¦ÌM).The 'X' at position 6 and 13 indicates (S)-a-2-(2'-pentenyl)alanine, X(6) and X(13) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03252	AQAWKXWATETLXVAN	16	Sequence 16 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50=9.3 ¡À 1.6 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50>130 ¦ÌM).The 'X' at position 6 and 13 indicates (S)-a-2-(2'-pentenyl)alanine, X(6) and X(13) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03253	IAQAKVEXWMTXTLLVAN	18	Sequence 17 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	"The peptide shows antiviral activity against HIV-1 IIIB(IC50=7.2 ¡À 1.2 ¦ÌM) and exhibits cytotoxicity against MT-2 cells(CC50>124.4 ¦ÌM).The 'X' at position 8 and 12 indicates (S)-a-2-(2'-pentenyl)alanine, X(8) and X(12) are cross-linked by hydrocarbon stapling."	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03254	AQAVKNWMTETLLVA	15	Sequence 19 from Patent US 20090281041	Synthetic construct	HIV	Patent Application	US 2009/0281041 A1	2009-11-12	CA 2725227 A1##WO 2009/137532 A1##AU 2009/244400 A1##US 2009/0281041 A1##AU 2009/244400 A2##EP 2283033 A1##JP 2011522796 A##US 8324153 B2##AU 2009/244400 B2##US 2013/0059776 A1##US 8933019 B2	Antiviral Cell-Penetrating Peptides	No cooments found in patent	Disclosed herein are cell penetrating peptides useful as treatment for Human Immunodeficiency Virus.
DRAVP03255	RRKKAAVALLPAVLLALLAP	20	Sequence 1 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	95 ¡À 2% inhibition against influenza virus at 10 ¦ÌM.(EC50= 2.6 ¡À 1.0 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03256	RRKKAAVALLPAVLLALLA	19	Sequence 2 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	94 ¡À 2% inhibition against influenza virus at 10 ¦ÌM.(EC50=0.5 ¡À 0.3 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03257	RRKKAAVALLPAVLLALL	18	Sequence 3 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	95 ¡À 2% inhibition against influenza virus at 10 ¦ÌM.(EC50= 0.6 ¡À 0.3 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03258	RRKKAAVALLPAVLLAL	17	Sequence 4 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	89 ¡À 3% inhibition against influenza virus at 10 ¦ÌM.(EC50= 3.8 ¡À 1.9 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03259	RRKKAAVALLPAVLLA	16	Sequence 5 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	96 ¡À 3% inhibition against influenza virus at 10 ¦ÌM.(EC50= 2.8 ¡À 1.1 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03260	RRKKAAVALLPAVLL	15	Sequence 6 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03261	RRKKAAVALLPAVL	14	Sequence 7 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03262	RRKKAAVALLPAV	13	Sequence 8 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03263	RRKKAAVALLPA	12	Sequence 9 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03264	RRKKAAVALLP	11	Sequence 10 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	4 ¡À 8% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03265	RRKKAAVALL	10	Sequence 11 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03266	RRKKAAVAL	9	Sequence 12 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03267	RRKKAAVA	8	Sequence 13 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03268	RRKKAAV	7	Sequence 14 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03269	RRKKAA	6	Sequence 15 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03270	RRKKA	5	Sequence 16 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03271	RRKK	4	Sequence 17 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03272	RRKKAVALLPAVLLALLAP	19	Sequence 18 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	94 ¡À 6% inhibition against influenza virus at 10 ¦ÌM.(EC50= 0.8 ¡À 0.3 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03273	RRKKVALLPAVLLALLAP	18	Sequence 19 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	94 ¡À 4% inhibition against influenza virus at 10 ¦ÌM.(EC50= 0.5 ¡À 0.4 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03274	RRKKALLPAVLLALLAP	17	Sequence 20 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	94 ¡À 3% inhibition against influenza virus at 10 ¦ÌM.(EC50= 0.7¡À 0.3 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03275	RRKKLLPAVLLALLAP	16	Sequence 21 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	94¡À 4% inhibition against influenza virus at 10 ¦ÌM.(EC50=0.8 ¡À 0.3 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03276	RRKKLPAVLLALLAP	15	Sequence 22 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	94 ¡À 4% inhibition against influenza virus at 10 ¦ÌM.(EC50= 0.9 ¡À 0.3 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03277	RRKKVLLALLAP	12	Sequence 23 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	90 ¡À 4% inhibition against influenza virus at 10 ¦ÌM.(EC50=4.0 ¡À 0.8 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03278	RRKKLLALLAP	11	Sequence 24 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03279	RRKKALLAP	9	Sequence 25 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03280	RRKKLLAP	8	Sequence 26 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03281	RRKKLAP	7	Sequence 27 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03282	RRKKAP	6	Sequence 28 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03283	RRKKP	5	Sequence 29 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03284	RRKKAALLVLAALAVLA	17	Sequence 30 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03285	RRKKLAALPLVLAAPLAVLA	20	Sequence 31 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03286	RRKKVALLAVLLALLA	16	Sequence 32 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	94 ¡À 4% inhibition against influenza virus at 10 ¦ÌM.(EC50= 0.5 ¡À 0.5 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03287	RRKKAAVALLAVLLALLA	18	Sequence 43 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	95 ¡À 2% inhibition against influenza virus at 10 ¦ÌM.(EC50=1.6 ¡À 1.2 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03288	RRKKLLAVLLALLA	14	Sequence 44 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	95 ¡À 2% inhibition against influenza virus at 10 ¦ÌM.(EC50= 3 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03289	RRKKLAVLLALLA	13	Sequence 45 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	94 ¡À 0% inhibition against influenza virus at 10 ¦ÌM.(EC50= 3 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03290	RRKKAAAAAAAAA	13	Sequence 49 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	87.5% inhibition against influenza virus at 10 ¦ÌM.(EC50~7 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03291	RKKLAVLLALLA	12	Sequence 50 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	75% inhibition against influenza virus at 10 ¦ÌM.(EC50=8 ¦ÌM)	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03292	RKAVLLALLA	10	Sequence 51 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	50% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03293	KLAVLLALLA	10	Sequence 52 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	25% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03294	KKLAVLLALLA	11	Sequence 53 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03295	EEDDLAVLLALLA	13	Sequence 54 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03296	RRKKLAVAAALLA	13	Sequence 55 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03297	RRKKLAVLLAAAA	13	Sequence 56 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	0% inhibition against influenza virus at 10 ¦ÌM.	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."
DRAVP03298	EEDD	4	Sequence 61 from Patent US 20100041604	Synthetic construct	Influenza Virus	Patent Application	US 2010/0041604 A1	2010-02-18	CA 2727898 A1##WO 2009/152519 A2##US 2010/0041604 A1##WO 2009/152519 A3##EP 2310030 A2##JP 2011524373 A##US 8129499 B2##US 2013/0190228 A1##EP 2310030 A4##US 9221874 B2	Novel Antiviral Peptides Against Influenza Virus	No comments found in patent	"The present disclosure generally relates to peptides having antiviral properties. More particularly, the invention relates to peptides exhibiting activity against influenza viruses, to pharmaceutical compositions comprising the peptides, and to methods of using the peptides to prevent and/or treat influenza viral infections."