发明名称 GnRH analogs
摘要 Peptides which include unnatural amino acids and which either promote or inhibit the secretion of gonadotropins by the pituitary gland and inhibit the release of steroids by the gonads. Administration of an effective amount of such peptides that are GnRH antagonists prevents ovulation of female mammalian eggs and/or the release of steroids by the gonads and may be used to treat steroid-dependent tumors. The agonists can be used for control of reproduction processes, to treat precocious puberty, endometriosis, and the like. The peptides are analogs of the decapeptide GnRH wherein there is at least one residue of an unnatural amino acid in the 3-, 5-, 6- and/or 8-positions. Unnatural amino acids having the following formula are incorporated in a preferred group of synthesized peptides: <IMAGE> with j = 1, 2 or 3. Methods for synthesizing such peptides having the triazole side chains are disclosed wherein one side chain modification (or two simultaneously) is carried out on an amino-substituted phenylalanine residue in a peptide chain which is a part of a peptidoresin.
申请公布号 US5580957(A) 申请公布日期 1996.12.03
申请号 US19940210619 申请日期 1994.03.18
申请人 THE SALK INSTITUTE FOR BIOLOGICAL STUDIES 发明人 HOEGER, CARL A.;RIVIER, JEAN E. F.;THEOBALD, PAULA G.;PORTER, JOHN S.;RIVIER CATHERINE LAURE;VALE WYLIE WALKER JR
分类号 A61K38/00;C07C277/08;C07C279/24;C07C279/28;C07C313/30;C07D249/14;C07K7/02;C07K7/23;(IPC1-7):C07K14/695 主分类号 A61K38/00
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