Kinase inhibitors and associated pharmaceutical compositions and methods of use
    9.
    发明授权
    Kinase inhibitors and associated pharmaceutical compositions and methods of use 有权
    激酶抑制剂及其相关药物组合物和使用方法

    公开(公告)号:US07232842B2

    公开(公告)日:2007-06-19

    申请号:US10754433

    申请日:2004-01-09

    CPC分类号: C07D487/04

    摘要: The invention provides novel compounds useful as kinase inhibitors or as starting materials And/or intermediates in the synthesis of compounds useful as kinase inhibitors. The compounds have The general structure of formula (I) wherein A is a 3- to 8-membered ring, optionally substituted and/or heteroatom-containing, and R1, R2, R3, R4, R5, R6, X, Y, Z, p, and q are as defined herein. The compounds may also be in the form of a salt, ester, amide, or other analog. In preferred compounds, A is a 5- to 8-membered ring, R1 is hydrogen, q is a bond, X is N, Y is C═O, Z is N, R2 contains a terminal amino moiety, p is 1, and R3 and R4 are linked to form a pyrrole ring fused to a second cyclic group. Pharmaceutical compositions and methods for using the compounds are also provided.

    摘要翻译: 本发明提供了可用作激酶抑制剂或作为起始物质的新化合物和/或合成可用作激酶抑制剂的化合物的中间体。 化合物具有式(I)的通式,其中A为任选被取代和/或含杂原子的3至8元环,R 1,R 2, R S,R 3,R 4,R 5,R 6,X,Y,Z,p ,和q如本文所定义。 化合物也可以是盐,酯,酰胺或其它类似物的形式。 在优选的化合物中,A是5-至8-元环,R 1是氢,q是一个键,X是N,Y是CO,Z是N,R 2, / SUP>含有末端氨基部分,p为1,R 3和R 4连接形成与第二个环状基团稠合的吡咯环。 还提供了使用该化合物的药物组合物和方法。