首页> 外国专利> CHOLESTEROL BIOSYNTHESIS INHIBITOR CONTAINING TRICYCLIC COMPOUND HAVING SPIRO UNION AS EFFECTIVE COMPONENT

CHOLESTEROL BIOSYNTHESIS INHIBITOR CONTAINING TRICYCLIC COMPOUND HAVING SPIRO UNION AS EFFECTIVE COMPONENT

机译:以螺环为有效成分的含有三环化合物的胆固醇生物合成抑制剂

摘要

Orally administrable cholesterol biosynthesis inhibitors exhibiting potentserum cholesterol lowering effect, which inhibitors contain as the activeingredient tricyclic spiro compounds represented by the general formula (I) orsalts thereof: (I) wherein A is a 5- or 6-membered heterocyclic group or thelike; B is a single bond, carbonyl, or the like; D is hydrogen or the like; Xis nitrogen or the like; Y is oxygen, -NH-, or the like; Z is methylene,carbonyl, or the like; T is -SO2-, carbonyl, or the like; Q is a hydrocarbongroup or a heterocyclic group; l, m, and n are each an integer of 0 to 2, withthe proviso that both l and m are not 0 simultaneously; and r is 0 or 1.
机译:口服有效的胆固醇生物合成抑制剂,显示有效降低血清胆固醇的作用,该抑制剂含有通式(I)表示的成分三环螺化合物或其盐:(I)其中A为5或6元杂环基或喜欢; B是单键,羰基等。 D为氢等。 X是氮等; Y为氧,-NH-等。 Z是亚甲基羰基等; T是-SO 2-,羰基等。 Q是碳氢化合物基团或杂环基团; l,m和n均为0到2的整数,其中l和m都不同时为0的条件;并且r为0或1。

著录项

  • 公开/公告号CA2433174A1

    专利类型

  • 公开/公告日2002-07-11

    原文格式PDF

  • 申请/专利权人 MOCHIDA PHARMACEUTICAL CO. LTD.;

    申请/专利号CA20012433174

  • 发明设计人 NISHIDA HIDEMITSU;MUKAIHIRA TAKAFUMI;

    申请日2001-12-28

  • 分类号C07D498/20;C07D221/00;C07D241/00;C07D263/00;A61P43/00;C07D487/04;A61P3/06;C07D498/10;C07D513/10;A61P9/10;A61P31/10;C07D471/20;C07D513/20;A61K31/4985;A61K31/506;A61K31/519;A61K31/537;A61K31/547;A61K31/55;A61K31/551;

  • 国家 CA

  • 入库时间 2022-08-22 00:40:36

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