发明名称 OXYTOCINANALOGER MED NATRIURETISK EFFEKT
摘要 Analogs of oxytocin of general formula I <IMAGE> where all amino acids are L-isomers and X is phenylalanine or phenylalanine substituted in the p-position by alkyl, ethoxy, amino, substituted amino, or nitro group, suitable for medical applications, and a method for their preparation consisting in the cyclization of linear octapeptides of general formula II <IMAGE> where X has the aforesaid meaning and Act is a group activating the carboxylic group of S-carboxyethylhomocysteine residue, e.g. an active ester. Two methods may be used for the preparation of [2-p-aminophenylalanine] deamino-6-carba-oxytocin, either the reduction of [2-p-nitrophenylalanine]- deamino-6-carba-oxytocin or deprotection of [2-p- benzyloxycarbonylaminophenylalanine] deamino-6-carba-oxytocin.
申请公布号 SE448303(B) 申请公布日期 1987.02.09
申请号 SE19810003778 申请日期 1981.06.16
申请人 CESKOSLOVENSKA AKADEMIE VED 发明人 1)M * LEBL;2)K * JOST;3)A * MACHOVA;4)P * HRBAS;5)J * SKOPKOVA;6)J * SLANINOVA;7)T * BARTH
分类号 C07K14/655;A61K38/00;A61K38/11;C07K1/02;C07K1/113;C07K7/16;C07K14/575;(IPC1-7):C07K7/16 主分类号 C07K14/655
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