首页> 外国专利> 9-FLUORO-PROSTAGLANDIN DERIVATIVES,PROCESS FOR THEIR MANUFACTURE AND PHARMACEUTICAL PREPARATIONS CONTAINING THEM

9-FLUORO-PROSTAGLANDIN DERIVATIVES,PROCESS FOR THEIR MANUFACTURE AND PHARMACEUTICAL PREPARATIONS CONTAINING THEM

机译:9-氟-前列腺素衍生物,其制备方法和包含它们的药物制剂

摘要

9-fluoroprostane derivatives of Formula I IMAGE (I) wherein R1 is CH2OH or IMAGE wherein R2 is hydrogen, alkyl, cycloalkyl, aryl, or a heterocyclic residue; or R1 is the residue IMAGE wherein R3 is an acid residue or R2 and A is -CH2-CH2- or cis-CH=CH-, B is -CH2-CH2-, trans-CH=CH- or -C 3BOND C, W is a free or functionally modified hydroxymethylene group wherein the OH-group can be in the alpha - or beta - position, D and E jointly are a direct bond or D is straight-chain or branched alkylene or alkenylene of 1-10 carbon atoms which can optionally be substituted by fluorine atoms, and E is oxygen or sulfur, a direct bond, -C 3BOND C- or -CR6=CR7- wherein R6 and R7 differ from each other and each is hydrogen, chlorine, or alkyl, R4 is a free or functionally modified hydroxy group, and R5 is hydrogen, an optionally substituted aliphatic group, e.g., alkyl or halosubstituted alkyl, cycloalkyl, optionally substituted aryl or a heterocyclic group, and, when R2 is H, the physiologically compatible salts thereof with bases, have valuable pharmacological properties, e.g., as luteolytics or abortifacients.
机译:式I的9-氟代前列腺素衍生物,其中R 1是CH 2 OH或其中R 2是氢,烷基,环烷基,芳基或杂环残基的;或R1为残基,其中R3为酸残基或R2且A为-CH2-CH2-或顺式-CH = CH-,B为-CH2-CH2-,反式-CH = CH-或-C 3BOND C,W是游离的或官能改性的羟甲基,其中OH-基团可以在α-或β-位,D和E共同为直接键或D为1-10的直链或支链亚烷基或亚烯基可以任选地被氟原子取代的碳原子,并且E是氧或硫,直接键,-C 3BOND C-或-CR6 = CR7-,其中R6和R7彼此不同并且各自是氢,氯或烷基,R 4是游离或官能改性的羟基,并且R 5是氢,任选取代的脂族基,例如烷基或卤代烷基,环烷基,任选取代的芳基或杂环基,并且当R 2为H时,是生理相容性盐其具有碱的碱具有有价值的药理性质,例如作为溶血药或流产药。

著录项

  • 公开/公告号IL66165A

    专利类型

  • 公开/公告日1986-01-31

    原文格式PDF

  • 申请/专利权人 SCHERING AG;

    申请/专利号IL19820066165

  • 发明设计人

    申请日1982-06-29

  • 分类号C07C177/00;A61K31/557;

  • 国家 IL

  • 入库时间 2022-08-22 07:41:23

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