Pyrimidine-Substituted Benzimidazole Derivatives as Protein Kinase Inhibitors
    8.
    发明申请
    Pyrimidine-Substituted Benzimidazole Derivatives as Protein Kinase Inhibitors 失效
    嘧啶取代的苯并咪唑衍生物作为蛋白激酶抑制剂

    公开(公告)号:US20080255112A1

    公开(公告)日:2008-10-16

    申请号:US11915148

    申请日:2006-06-30

    摘要: The invention provides a novel class of compounds, pharmaceutical compositions comprising such compounds and methods of using such compounds to treat or prevent diseases or disorders associated with abnormal or deregulated kinase activity, particularly diseases or disorders that involve abnormal activation of Alk, Abl, BRK, Blk, BMX, CSK, c-Src, c-Raf, EGFR, Fes, FGFR3, Fms, Fyn, IGF-IR, IR, IKKα, IKKβ, JAK2, JAK3, KDR, Lck, Met, p70S6k, Ros, Rsk1, SAPK2α, SAPK2β, SAPK3, SIK, Tie2, TrkB and/or WNK3 kinases.

    摘要翻译: 本发明提供了一类新颖的化合物,包含这些化合物的药物组合物和使用这些化合物治疗或预防与异常或失调的激酶活性相关的疾病或病症的方法,特别是涉及Alk​​,Abl,BRK, 大肠杆菌,BMX,CSK,c-Src,c-Raf,EGFR,Fes,FGFR3,Fms,Fyn,IGF-IR,IR,IKKalpha,IKKbeta,JAK2,JAK3,KDR,Lck,Met,p70S6k,Ros,Rsk1, SAPK2alpha,SAPK2beta,SAPK3,SIK,Tie2,TrkB和/或WNK3激酶。