where   X is CH or N;   Y is O or S;   R¹ is 2-propenyl, C₁-C₃ alkyl, benzyl or substituted benzyl where the substitutents are one or two of the same or different and are selected from methyl, ethyl, methoxy, ethoxy, hydroxy, chloro, bromo, or fluoro;   R₂ is C₂-C₃ alkyl, allyl or cyclopropylmethyl;   R³ and R⁴ are both hydrogen or combine to form a carbon-carbon bond; and pharmaceutically acceptable acid addition salts thereof to a mammal requiring bone demineralization inhibition."/> Use of ergoline derivatives for the treatment of diseases associated with bone demineralization
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Use of ergoline derivatives for the treatment of diseases associated with bone demineralization

机译:麦角灵衍生物在治疗与骨脱矿有关的疾病中的用途

摘要

A method of inhibiting bone demineralization comprising administration of an effective amount of a compound having the formula where   X is CH or N;   Y is O or S;   R¹ is 2-propenyl, C₁-C₃ alkyl, benzyl or substituted benzyl where the substitutents are one or two of the same or different and are selected from methyl, ethyl, methoxy, ethoxy, hydroxy, chloro, bromo, or fluoro;   R₂ is C₂-C₃ alkyl, allyl or cyclopropylmethyl;   R³ and R⁴ are both hydrogen or combine to form a carbon-carbon bond; and pharmaceutically acceptable acid addition salts thereof to a mammal requiring bone demineralization inhibition.
机译:抑制骨脱矿质的方法,包括施用有效量的具有下式的化合物 <图像文件=“ IMGA0001.GIF” he =“ 66” imgContent =“ chem” imgFormat =“ GIF” wi =“ 93” /> 哪里X为CH或N;Y是O或S;R 1是2-丙烯基,C 1 -C 4烷基,苄基或取代的苄基,其中取代基是相同或不同的一个或两个,并且选自甲基,乙基,甲氧基,乙氧基,羟基,氯,溴或氟;R 2是C 2 -C 6烷基,烯丙基或环丙基甲基;R 3和R 5都是氢或结合形成碳-碳键;及其药学上可接受的酸加成盐给需要抑制骨矿物质化的哺乳动物。

著录项

  • 公开/公告号EP0458640A2

    专利类型

  • 公开/公告日1991-11-27

    原文格式PDF

  • 申请/专利权人 ELI LILLY AND COMPANY;

    申请/专利号EP19910304693

  • 发明设计人 BRYANT HENRY UHLMAN;CLEMENS JAMES ALLEN;

    申请日1991-05-23

  • 分类号A61K31/48;

  • 国家 EP

  • 入库时间 2022-08-22 05:30:39

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