c-Met


c-Met (tyrosine-protein kinase,HGFR) is a protein that possesses tyrosine kinase activity. The primary single chain precursor protein is post-translationally cleaved to produce the alpha and beta subunits, which are disulfide linked to form the mature receptor. MET is a single pass tyrosine kinase receptor essential for embryonic development, organogenesis and wound healing. Hepatocyte growth factor/Scatter Factor (HGF/SF) and its splicing isoform (NK1, NK2) are the only known ligands of the MET receptor. MET is normally expressed by cells of epithelial origin, while expression of HGF/SF is restricted to cells of mesenchymal origin. When HGF/SF binds its cognate receptor MET it induces its dimerization through a not yet completely understood mechanism leading to its activation.
  • BMS-794833 EY0835

    BMS-794833是Met/VEGFR2高效ATP竞争性抑制剂,IC50值为1.7/15 nM,还能抑制Ron, Axl和Flt3的活性,是BMS-817378的前体药物。

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  • MK-2461 EY0673

    MK-2461是一种有效的,多靶点抑制剂,作用于c-Met(WT/mutants),IC50为0.4-2.5 nM,对Ron,和Flt1作用效果稍弱;作用于c-Met比作用于FGFR1, FGFR2, FGFR3, PDGFRβ, KDR, Flt3, Flt4, TrkA和TrkB选择性高8到30倍。Phase 1/2。

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  • JNJ-38877605 EY0407

    JNJ-38877605是一种ATP竞争性的c-Met抑制剂,IC50为4 nM,作用于c-Met比作用于200种其他酪氨酸和丝-苏氨酸激酶选择性高600倍。

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  • AMG-208 EY0280

    AMG-208是一种高度选择性的c-Met抑制剂,IC50为9 nM。

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