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Pyridyl acetic acid Compounds, Pharmaceutical Agent and use of said Compound for preparing Agent

机译:吡啶基乙酸化合物,药剂和该化合物在制备药剂中的用途

摘要

This table provides a compound represented by formula (1), wherein R1 is an optional C1-6 tar group, replaced by a c3-10 cyclopropyl group; R2 is C1-6 tar; R3 is an H atom, C1-6 tar or a halogenated atom; X is - or6 o-nr4r5, wherein R5 and R6 are each an independent H atom. Optional replacement group of hydrocarbons or optional heterocyclic replacement group; R5 is optional replacement group of hydrocarbons, optional heterocyclic replacement group or optional replacement group of hydrocarbons, or R4 and R5 are optionally formed together with adjacent atoms, An alternative heterosexualOr their salt At present, the compound has a high concentration of cucumber inhibition, which is a useful preventive or therapeutic agent for diabetes.
机译:该表提供了由式(1)表示的化合物,其中R 1是任选的C 1-6焦油基团,被c 3-10环丙基取代; R2为C1-6焦油; R 3是H原子,C 1-6焦油或卤原子; X为-或6-o-nr4r5,其中R5和R6各自为独立的H原子。烃的任选取代基或任选杂环取代基; R5是烃的任选取代基,烃的任选杂环取代基或任选取代基,或R4和R5任选与相邻原子一起形成。替代杂性或其盐目前,该化合物具有高浓度的黄瓜抑制作用,其中是有用的糖尿病预防或治疗剂。

著录项

  • 公开/公告号AR055563A1

    专利类型

  • 公开/公告日2007-08-22

    原文格式PDF

  • 申请/专利权人 TAKEDA PHARMACEUTICAL COMPANY LIMITED;

    申请/专利号AR2006P100686

  • 发明设计人 MAEZAKI HIRONOBU;SUZUKI N.;

    申请日2006-02-24

  • 分类号C07D213/55;C07D213/56;C07D401/12;C07D401/14;C07D405/12;C07D409/12;C07D413/12;C07D417/12;A61K31/44;A61K31/4427;A61P5/50;

  • 国家 AR

  • 入库时间 2022-08-21 20:59:36

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