首页> 外国专利> 1,3,4 - thiadiazole compounds and - 1,3,4 Oxadiazoles,The preparation method and Pharmaceutical compositions useful as inhibitors of phosphodiesterase (PDE) - 7 - (7) for the treatment of diseases related to t cells.Autoimmune diseases, inflammatory, pulmonary, CNS, allergies, cancer and AIDS.

1,3,4 - thiadiazole compounds and - 1,3,4 Oxadiazoles,The preparation method and Pharmaceutical compositions useful as inhibitors of phosphodiesterase (PDE) - 7 - (7) for the treatment of diseases related to t cells.Autoimmune diseases, inflammatory, pulmonary, CNS, allergies, cancer and AIDS.

机译:1,3,4-噻二唑化合物和-1,3,4恶二唑,其制备方法和药物组合物可用作磷酸二酯酶(PDE)抑制剂-7-(7),用于治疗与t细胞有关的疾病。炎症,肺部,中枢神经系统,过敏,癌症和艾滋病。

摘要

The Invention provides 1.3,4 - Oxadiazoles having the following formula (i) where:And it s or u, R1 is alkyl, alquenilo, alquinilo, cycloalkyl, aryl, heterocicloalquilo, cicloalquenilo,Or a polycyclic heteroaryl Group, R2 is alkyl, optionally substituted, alquenilo, alquinilo heterocicloalquilo, cycloalkyl, aryl, heteroaryl, cicloalquenilo,Polycyclic group or an optionally substituted, or their Derivatives, pharmaceutically acceptableThe process for their Preparation and their use for the manufacture of a Medicament for the treatment of disorders for which Treatment with an inhibitor of PDE7 is relevant.
机译:本发明提供了具有下式(i)的1.3,4-恶二唑:其中,s为或u,R 1为烷基,alquenilo,alquinilo,环烷基,芳基,杂环氯基,cicloalquenilo或多环杂芳基,R 2为烷基,任选地药学上可接受的取代的,alquenilo,alquinilo杂环氯基,环烷基,芳基,杂芳基,cicloalquenilo,多环基团或它们的衍生物或其衍生物药学上可接受的制备方法及其在制备用于治疗疾病的药物中的用途PDE7的抑制剂是相关的。

著录项

  • 公开/公告号CL2001002338A1

    专利类型

  • 公开/公告日2002-05-24

    原文格式PDF

  • 申请/专利权人 WARNER-LAMBERT COMPANY;

    申请/专利号CL2001002338

  • 申请日2001-09-27

  • 分类号A61K31/4245;A61K31/433;A61K31/439;A61K31/4439;A61K31/4709;A61K31/497;A61K31/55;A61P29/00;C07D207/14;C07D271/113;C07D285/135;C07D417/04;C07D417/10;C07D417/12;C07D417/14;C07D453/02;

  • 国家 CL

  • 入库时间 2022-08-22 00:45:56

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