Novel substituted indolines with an inhibitory effect on various kinases and complexes of CDKs
    1.
    发明申请
    Novel substituted indolines with an inhibitory effect on various kinases and complexes of CDKs 有权
    新型取代的吲哚啉对CDK的各种激酶和复合物具有抑制作用

    公开(公告)号:US20040058978A1

    公开(公告)日:2004-03-25

    申请号:US10666643

    申请日:2003-09-19

    IPC分类号: C07D209/36 A61K031/404

    摘要: The present invention relates to new substituted indolinones of general formula 1 wherein X and R1 to R5 are defined as in claim 1, the isomers and the salts thereof which have valuable properties. The above compounds of general formula I wherein R1 denotes a hydrogen atom, a C1-3-alkyl group or a prodrug group have valuable pharmacological properties, particularly an inhibiting effect on various kinases, on viral cyclin and on receptor tyrosine kinases, and the other compounds of the above general formula I wherein R1 does not represent a hydrogen atom, a C1-3-alkyl group or a prodrug group are valuable intermediate products for the preparation of the abovementioned compounds.

    摘要翻译: 本发明涉及通式的新的取代的二氢吲哚酮,其中X和R 1至R 5如权利要求1所定义,其异构体及其盐具有有价值的性质。 其中R1表示氢原子,C1-3烷基或前药基团的上述通式I化合物对病毒细胞周期蛋白和受体酪氨酸激酶具有有价值的药理学特性,特别是对各种激酶的抑制作用,另外 其中R1不表示氢原子,C1-3烷基或前药基团的上述通式I的化合物是制备上述化合物的有价值的中间产物。