首页> 外国专利> 4 AMINO 5 CYANO 2 ANILINO PYRIMIDINE DERIVATIVES AND THEIR USE AS INHIBITORS OF CELL CYCLE KINASES.

4 AMINO 5 CYANO 2 ANILINO PYRIMIDINE DERIVATIVES AND THEIR USE AS INHIBITORS OF CELL CYCLE KINASES.

机译:4氨基酸5氰基2苯胺嘧啶衍生物及其作为细胞周期激酶抑制剂的用途。

摘要

Compounds of formula (I) wherein: R1 is halo, nitro, cyano, hydroxy, amino, carboxy, carbamoyl, mercapto, C1 6alkyl, C2 6alkenyl or C2 6alkynyl; p is 0 4; wherein the values of R1 may be the same or different; R2 is sulphamoyl or a group B E ; wherein B is optionally substituted as defined within and is selected from C1 6alkyl, C2 6alkenyl, C2 6alkynyl, C3 8cycloalkyl, C1 6alkyl, phenyl, a heterocyclic group, phenylC1 6alkyl or (heterocyclic group)C1 6alkyl; E is C(O) , N(Ra)C(O) , C(O)N(Ra) , S(O)r , SO2N(Ra) or N(Ra)SO2 ; wherein Ra is hydrogen or C1 6alkyl optionally substituted as defined within and r is 1 2; q is 0 2; wherein the values of R2 may be the same or different; and wherein p plus; q = 1 5; or a pharmaceutically acceptable salt or an in vivo hydrolysable ester thereof are described. Processes for their manufacture and their use as inhibitors of cell cycle kinases, particularly CDK2, CDK4 and or CDK6 are also described.
机译:式(I)的化合物,其中:R 1为卤素,硝基,氰基,羟基,氨基,羧基,氨基甲酰基,巯基,C 1-6烷基,C 2-6烯基或C 2-6炔基; p是0 4;其中R1的值可以相同或不同; R2是氨磺酰基或基团B E;其中B是如在本文中所定义的那样任选地被取代并且选自C 1 6烷基,C 2 6烯基,C 2 6炔基,C 3 8环烷基,C 1 6烷基,苯基,杂环基,苯基C 1 6烷基或(杂环基)C 1 6烷基; E为C(O),N(Ra)C(O),C(O)N(Ra),S(O)r,SO2N(Ra)或N(Ra)SO2;其中Ra是氢或如在定义中任选被取代的C 1-6烷基,r是1 2; q是0 2;其中R2的值可以相同或不同;并且其中p加; q = 1 5;描述了其药学上可接受的盐或其体内可水解的酯。还描述了其制备方法及其用作细胞周期激酶,特别是CDK2,CDK4和或CDK6的抑制剂的用途。

著录项

  • 公开/公告号MXPA02009255A

    专利类型

  • 公开/公告日2003-03-12

    原文格式PDF

  • 申请/专利权人 ASTRAZENECA AB;

    申请/专利号MX2002PA09255

  • 发明设计人 THOMAS ANDREW PETER;

    申请日2001-03-23

  • 分类号A61K31/505;C07D239/48;C07D401/12;C07D403/12;C07D405/12;C07D413/12;A61P35/00;

  • 国家 MX

  • 入库时间 2022-08-22 00:02:16

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