Imidazo[1,2-b]pyridazine derivatives as kinase inhibitors
    4.
    发明授权
    Imidazo[1,2-b]pyridazine derivatives as kinase inhibitors 有权
    咪唑并[1,2-b]哒嗪衍生物作为激酶抑制剂

    公开(公告)号:US09187489B2

    公开(公告)日:2015-11-17

    申请号:US14378318

    申请日:2013-06-03

    IPC分类号: C07D487/04

    CPC分类号: C07D487/04

    摘要: The present invention is intended to provide a compound or a pharmacologically acceptable salt thereof which is useful in the treatment of a tumor through its ROS1 kinase enzyme activity inhibitory effect and NTRK kinase enzyme inhibitory effect. The present invention provides a compound having an imidazo[1,2-b]pyridazine structure represented by the general formula (I) or a pharmacologically acceptable salt thereof, and a pharmaceutical composition comprising the compound. In the formula, R1, G, T, Y1, Y2, Y3, and Y4 are as defined herein.

    摘要翻译: 本发明旨在提供其可用于通过其ROS1激酶活性抑制作用和NTRK激酶抑制作用治疗肿瘤的化合物或其药理学上可接受的盐。 本发明提供具有由通式(I)表示的咪唑并[1,2-b]哒嗪结构或其药学上可接受的盐的化合物和包含该化合物的药物组合物。 在该式中,R1,G,T,Y1,Y2,Y3和Y4如本文所定义。

    IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AS KINASE INHIBITORS
    8.
    发明申请
    IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AS KINASE INHIBITORS 有权
    咪唑并[1,2-b]吡啶衍生物作为激酶抑制剂

    公开(公告)号:US20150051190A1

    公开(公告)日:2015-02-19

    申请号:US14378318

    申请日:2013-06-03

    IPC分类号: C07D487/04

    CPC分类号: C07D487/04

    摘要: The present invention is intended to provide a compound or a pharmacologically acceptable salt thereof which is useful in the treatment of a tumor through its ROS1 kinase enzyme activity inhibitory effect and NTRK kinase enzyme inhibitory effect. The present invention provides a compound having an imidazo[1,2-b]pyridazine structure represented by the general formula (I) or a pharmacologically acceptable salt thereof, and a pharmaceutical composition comprising the compound. In the formula, R1, G, T, Y1, Y2, Y3, and Y4 are as defined herein.

    摘要翻译: 本发明旨在提供其可用于通过其ROS1激酶活性抑制作用和NTRK激酶抑制作用治疗肿瘤的化合物或其药理学上可接受的盐。 本发明提供具有由通式(I)表示的咪唑并[1,2-b]哒嗪结构或其药学上可接受的盐的化合物和包含该化合物的药物组合物。 在该式中,R1,G,T,Y1,Y2,Y3和Y4如本文所定义。