发明名称 Staphylococcus peptides for bacterial interference
摘要 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 NH<SUB>2</SUB>-X<SUB>(n)</SUB>-Z-X<SUB>(y)</SUB>-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.
申请公布号 US6953833(B2) 申请公布日期 2005.10.11
申请号 US20010032950 申请日期 2001.12.27
申请人 NEW YORK UNIVERSITY 发明人 MUIR TOM W.;MAYVILLE PATRICIA;NOVICK RICHARD P.;BEAVIS RONALD;JI GUANGYONG
分类号 A61K38/16;(IPC1-7):A61K38/12;A61K38/00;C07K16/00 主分类号 A61K38/16
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