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    • 3. 发明授权
    • Staphylococcus peptides for bacterial interference
    • 葡萄球菌肽用于细菌干扰
    • US07419954B2
    • 2008-09-02
    • US11212020
    • 2005-08-25
    • Tom W. MuirPatricia MayvilleRichard P. NovickRonald BeavisGuangyong Ji
    • Tom W. MuirPatricia MayvilleRichard P. NovickRonald BeavisGuangyong Ji
    • A61K38/00A61K38/12
    • C07K7/06A61K38/00C07K14/31
    • The present invention provides a cyclic peptide comprising the structure: wherein X is selected from the group consisting of an amino acid, an amino acid analog, a peptidomimetic and a non-amide isostere, Z is selected from the group consisting of a synthetic amino acid and a biosynthetic amino acid, R is selected from the group consisting of oxygen, nitrogen, sulfur and carbon, n is 0 to 10 and y is 1 to 10. The present invention also provides a cyclic peptide comprising the amino acid sequence of NH2—X(n)-Z-X(y)—COOH and a cyclic bond between the Z residue and COOH other than a thioester bond, wherein X is selected from the group consisting of to an amino acid, an amino acid analog, a peptidomimetic and a non-amide isostere, Z is selected from the group consisting of a synthetic amino acid and a biosynthetic amino acid, n is 0 to 10 and y is 1 to 10. Methods of preparation including a cyclization protocol, and methods of use of the cyclic peptides of the invention are also disclosed.
    • 本发明提供了包含以下结构的环肽:其中X选自氨基酸,氨基酸类似物,拟肽和非酰胺异基因,Z选自合成氨基酸 和生物合成氨基酸,R选自氧,氮,硫和碳,n为0至10,y为1至10.本发明还提供了包含氨基酸序列NH 4的环肽, (n)-ZX(y)-COOH和除了硫酯键之外的Z残基和COOH之间的环键,其中 X选自氨基酸,氨基酸类似物,拟肽和非酰胺异构体,Z选自合成氨基酸和生物合成氨基酸,n为0至10 和y为1至10.包括环化方案的制备方法和使用环状肽的方法 还公开了本发明。
    • 4. 发明申请
    • Novel Staphylococcus peptides for bacterial interference
    • 新型葡萄球菌肽用于细菌干扰
    • US20070185016A1
    • 2007-08-09
    • US11212020
    • 2005-08-25
    • Tom MuirPatricia MayvilleRichard NovickRonald BeavisGuangyong Ji
    • Tom MuirPatricia MayvilleRichard NovickRonald BeavisGuangyong Ji
    • A61K38/12A61K31/43A61K31/545
    • C07K7/06A61K38/00C07K14/31
    • The present invention provides a cyclic peptide comprising the structure: wherein X is selected from the group consisting of an amino acid, an amino acid analog, a peptidomimetic and a non-amide isostere, Z is selected from the group consisting of a synthetic amino acid and a biosynthetic amino acid, R is selected from the group consisting of oxygen, nitrogen, sulfur and carbon, n is 0 to 10 and y is 1 to 10. The present invention also provides a cyclic peptide comprising the amino acid sequence of NH2—X(n)-Z-X(y)—COOH and a cyclic bond between the Z residue and COOH other than a thioester bond, wherein X is selected from the group consisting of to an amino acid, an amino acid analog, a peptidomimetic and a non-amide isostere, Z is selected from the group consisting of a synthetic amino acid and a biosynthetic amino acid, n is 0 to 10 and y is 1 to 10. Methods of preparation including a cyclization protocol, and methods of use of the cyclic peptides of the invention are also disclosed.
    • 本发明提供了包含以下结构的环肽:其中X选自氨基酸,氨基酸类似物,拟肽和非酰胺异基因,Z选自合成氨基酸 和生物合成氨基酸,R选自氧,氮,硫和碳,n为0至10,y为1至10.本发明还提供了包含氨基酸序列NH 4的环肽, (n)-ZX(y)-COOH和除了硫酯键之外的Z残基和COOH之间的环键,其中 X选自氨基酸,氨基酸类似物,拟肽和非酰胺异构体,Z选自合成氨基酸和生物合成氨基酸,n为0至10 和y为1至10.包括环化方案的制备方法和使用环状肽的方法 还公开了本发明。
    • 5. 发明授权
    • Staphylococcus peptides for bacterial interference
    • 葡萄球菌肽用于细菌干扰
    • US06953833B2
    • 2005-10-11
    • US10032950
    • 2001-12-27
    • Tom W. MuirPatricia MayvilleRichard P. NovickRonald BeavisGuangyong Ji
    • Tom W. MuirPatricia MayvilleRichard P. NovickRonald BeavisGuangyong Ji
    • A61K38/16A61K38/12A61K38/00C07K16/00
    • A61K38/164
    • The present invention provides a cyclic peptide comprising the structure: wherein X is selected from the group consisting of an amino acid, an amino acid analog, a peptidomimetic and a non-amide isostere, Z is selected from the group consisting of a synthetic amino acid and a biosynthetic amino acid, R is selected from the group consisting of oxygen, nitrogen, sulfur and carbon, n is 0 to 10 and y is 1 to 10. The present invention also provides a cyclic peptide comprising the amino acid sequence of NH2—X(n)-Z-X(y)—COOH and a cyclic bond between the Z residue and COOH other than a thioester bond, wherein X is selected from the group consisting of an amino acid, an amino acid analog, a peptidomimetic and a non-amide isostere, Z is selected from the group consisting of a synthetic amino acid and a biosynthetic amino acid, n is 0 to 10 and y is 1 to 10. Methods of preparation including a cyclization protocol, and methods of use of the cyclic peptides of the invention are also disclosed.
    • 本发明提供了包含以下结构的环肽:其中X选自氨基酸,氨基酸类似物,拟肽和非酰胺异基因,Z选自合成氨基酸 和生物合成氨基酸,R选自氧,氮,硫和碳,n为0至10,y为1至10.本发明还提供了包含氨基酸序列NH 4的环肽, (n)-ZX(y)-COOH和除了硫酯键之外的Z残基和COOH之间的环键,其中 X选自氨基酸,氨基酸类似物,拟肽和非酰胺异构体,Z选自合成氨基酸和生物合成氨基酸,n为0至10,以及 y为1至10.制备方法包括环化方案,以及使用环状肽的方法 还公开了本发明。
    • 7. 发明授权
    • Staphylococcus peptides for bacterial interference
    • 葡萄球菌肽用于细菌干扰
    • US06337385B1
    • 2002-01-08
    • US09339511
    • 1999-06-24
    • Tom W. MuirPatricia MayvilleRichard P. NovickRonald BeavisGuangyong Ji
    • Tom W. MuirPatricia MayvilleRichard P. NovickRonald BeavisGuangyong Ji
    • A61K3812
    • A61K38/164
    • The present invention provides a cyclic peptide comprising the structure: wherein X is selected from the group consisting of an amino acid, an amino acid analog, a peptidomimetic and a non-amide isostere, Z is selected from the group consisting of a synthetic amino acid and a biosynthetic amino acid, R is selected from the group consisting of oxygen, nitrogen, sulfur and carbon, n is 0 to 10 and y is 1 to 10. The present invention also provides a cyclic peptide comprising the amino acid sequence of NH2—X(n)—Z—X(y)—COOH and a cyclic bond between the Z residue and COOH other than a thioester bond, wherein X is selected from the group consisting of an amino acid, an amino acid analog, a peptidomimetic and a non-amide isostere, Z is selected from the group consisting of a synthetic amino acid and a biosynthetic amino acid, n is 0 to 10 and y is 1 to 10. Methods of preparation including a cyclization protocol, and methods of use of the cyclic peptides of the invention are also disclosed.
    • 本发明提供了包含以下结构的环肽:其中X选自氨基酸,氨基酸类似物,拟肽和非酰胺异基因,Z选自合成氨基酸 和生物合成氨基酸,R选自氧,氮,硫和碳,n为0至10,y为1至10.本发明还提供了包含氨基酸序列NH2- X(n)-ZX(y)-COOH和除了硫酯键之外的Z残基和COOH之间的环键,其中X选自氨基酸,氨基酸类似物,肽模拟物和非 - 酰胺等离子体,Z选自合成氨基酸和生物合成氨基酸,n为0至10,y为1至10.包括环化方案的制备方法和环肽的使用方法 也公开了本发明。