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pyridyl and pyridimil substituted pyrrol, thiophene and furan derivatives as kinase inhibitors

机译:吡啶基和吡啶基取代的吡咯,噻吩和呋喃衍生物作为激酶抑制剂

摘要

B PIRROL, THIOPHENE AND FURAN DERIVATIVES REPLACED BY PYRIDIL AND PYRIDIMIL AS KINASE INHIBITORS D The present invention relates to the compounds of formula (1) below, or the pharmaceutically acceptable salts thereof, where G, W, R ~ 2 ~, R ~ 3 ~, R ~ 4 ~, R ~ 5 ~ and R ~ 6 ~ are as defined in the specification. The invention also relates to processes and intermediates for the preparation of the compounds of formula (1), pharmaceutical compositions comprising these and methods for treating cell proliferative disorders. The compounds of the formula (1) are useful, in therapy, in the treatment of diseases associated with unregulated protein kinase activity, such as cancer.
机译:被吡咯和吡啶取代的吡咯,噻吩和呋喃衍生物作为激酶抑制剂本发明涉及以下式(1)的化合物或其药学上可接受的盐,其中G,W,R 2〜 ,R〜3〜,R〜4〜,R〜5〜和R〜6〜如说明书中所定义。本发明还涉及用于制备式(1)的化合物的方法和中间体,包含这些化合物的药物组合物以及用于治疗细胞增殖性疾病的方法。式(1)的化合物可用于治疗与蛋白激酶活性失调有关的疾病,例如癌症。

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