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SUBSTITUTED QUINAZOLINE DERIVATIVES AND THEIR USE AS TYROSINE KINASE INHIBITORS

机译:取代的喹唑啉衍生物及其作为酪氨酸激酶抑制剂的用途

摘要

This invention provides compounds of formula (1) wherein X is C3-7 cycloalkyl, pyridinyl, pyrimidinyl or phenyl ring optionally substituted as described in claim 1, R1, R3 and R4 are chosen from the groups listed in claim 1. R2 is chosen from various unsaturated acyl groups listed in claim 1, with certain compounds being disclaimed. Use as tyrosine kinase inhibitors for the treatment of cancer and certain kidney diseases such as polycystic kidney disease.
机译:本发明提供了式(1)的化合物,其中X是如权利要求1所述的可被取代的C3-7环烷基,吡啶基,嘧啶基或苯环,R1,R3和R4选自权利要求1中列出的基团。权利要求1中列出的各种不饱和酰基,其中某些化合物被放弃。用作酪氨酸激酶抑制剂,用于治疗癌症和某些肾脏疾病,例如多囊肾。

著录项

  • 公开/公告号BE2014C023I2

    专利类型

  • 公开/公告日2018-01-10

    原文格式PDF

  • 申请/专利权人 WYETH HOLDINGS LLC.;

    申请/专利号BE2014C023C

  • 发明设计人

    申请日2014-03-14

  • 分类号A61K31/505;A61K31/517;A61K31/5377;A61P13/12;A61P35;A61P35/04;A61P43;C07D239/94;C07D401/12;C07D403/06;C07D405/12;C07D413/06;

  • 国家 BE

  • 入库时间 2022-08-21 12:54:13

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