2-HETEROARYLAMINO-PYRIMIDINE DERIVATIVES AS KINASE INHIBITORS
    8.
    发明申请
    2-HETEROARYLAMINO-PYRIMIDINE DERIVATIVES AS KINASE INHIBITORS 失效
    作为激酶抑制剂的2-异喹啉衍生物衍生物

    公开(公告)号:US20110053952A1

    公开(公告)日:2011-03-03

    申请号:US12673948

    申请日:2008-08-18

    摘要: The invention provides compounds of Formula (I) and pharmaceutical compositions thereof, which are useful as protein kinase inhibitors, as well as methods for using such compounds to treat, ameliorate or prevent a condition associated with abnormal or deregulated kinase activity. In some embodiments, the invention provides methods for using such compounds to treat, ameliorate or prevent diseases or disorders that involve abnormal activation of c-kit, PDGFRα, PDGFRβ, CSF1R, Abl, BCR-Abl, CSK, JNK1, JNK2, p38, p70S6K, TGFβ, SRC, EGFR, trkB, FGFR3, Fes, Lck, Syk, RAF, MKK4, MKK6, SAPK2β, BRK, Fms, KDR, c-raf or b-raf kinases.

    摘要翻译: 本发明提供了可用作蛋白激酶抑制剂的式(I)化合物及其药物组合物,以及使用这些化合物治疗,改善或预防与异常或失调激酶活性相关的病症的方法。 在一些实施方案中,本发明提供了使用这些化合物治疗,改善或预防涉及c-kit,PDGFRα,PDGFR和bgr,CSF1R,Abl,BCR-Abl,CSK,JNK1,JNK2,p38异常活化的疾病或病症的方法 ,p70S6K,TGF-bgr,SRC,EGFR,trkB,FGFR3,Fes,Lck,Syk,RAF,MKK4,MKK6,SAPK2&bgr; BRK,Fms,KDR,c-raf或b-raf激酶。