5-(4-(haloalkoxy)phenyl) pyrimidine-2-amine compounds and compositions as kinase inhibitors
    60.
    发明授权
    5-(4-(haloalkoxy)phenyl) pyrimidine-2-amine compounds and compositions as kinase inhibitors 有权
    5-(4-(卤代烷氧基)苯基)嘧啶-2-胺化合物和组合物作为激酶抑制剂

    公开(公告)号:US08293757B2

    公开(公告)日:2012-10-23

    申请号:US12674416

    申请日:2008-08-19

    摘要: The invention provides compounds of formula (1) 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, AbI, BCR-AbI, CSK, JNK1, JNK2, p38, p70S6K, TGFβ, SRC, EGFR, trkB, FGFR3. Fes, Lck, Syk, RAF, MKK4, MKK6, SAPK2β, BRK, Fms, KDR, c-rapor 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(1)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,AbI,BCR-AbI,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-rapor b-raf激酶。