Mitotic Kinesin Inhibitors
    52.
    发明申请
    Mitotic Kinesin Inhibitors 失效
    有丝分裂驱动蛋白抑制剂

    公开(公告)号:US20080194582A1

    公开(公告)日:2008-08-14

    申请号:US11886274

    申请日:2006-03-10

    CPC分类号: C07D231/06

    摘要: The present invention relates to dihydropyrazole compounds that are useful for treating cellular proliferative diseases, for treating disorders associated with KSP kinesin activity, and for inhibiting KSP kinesin. The invention also related to compositions which comprise these compounds, and methods of using them to treat cancer in mammals.

    摘要翻译: 本发明涉及可用于治疗细胞增殖性疾病,治疗与KSP驱动蛋白活性相关的疾病和用于抑制KSP驱动蛋白的二氢吡唑化合物。 本发明还涉及包含这些化合物的组合物,以及使用它们治疗哺乳动物癌症的方法。

    Mitotic Kinesin Inhibitors
    53.
    发明申请
    Mitotic Kinesin Inhibitors 审中-公开
    有丝分裂驱动蛋白抑制剂

    公开(公告)号:US20080102068A1

    公开(公告)日:2008-05-01

    申请号:US11795440

    申请日:2006-01-13

    CPC分类号: C07D495/04

    摘要: The present invention relates to fluorinated 2-aminomethylthienopyrimidinone compounds that are useful for treating cellular proliferative diseases, for treating disorders associated with KSP kinesin activity, and for inhibiting KSP kinesin. The invention also related to compositions which comprise these compounds, and methods of using them to treat cancer in mammals.

    摘要翻译: 本发明涉及可用于治疗细胞增殖性疾病,用于治疗与KSP驱动蛋白活性相关的病症和用于抑制KSP驱动蛋白的氟化2-氨基甲基噻吩并嘧啶酮化合物。 本发明还涉及包含这些化合物的组合物,以及使用它们治疗哺乳动物癌症的方法。

    Mitotic kinesin inhibitors
    54.
    发明授权
    Mitotic kinesin inhibitors 失效
    有丝分裂驱动蛋白抑制剂

    公开(公告)号:US07632839B2

    公开(公告)日:2009-12-15

    申请号:US11795435

    申请日:2006-01-13

    CPC分类号: C07D417/04

    摘要: The present invention relates to fluorinated aminoalkyl-4-oxo-3,4-dihydropyrido[3,4-d]pyrimidine derivatives that are useful for treating cellular proliferative diseases, for treating disorders associated with KSP kinesin activity, and for inhibiting KSP kinesin. The invention also related to compositions which comprise these compounds, and methods of using them to treat cancer in mammals.

    摘要翻译: 本发明涉及可用于治疗细胞增殖性疾病,用于治疗与KSP驱动蛋白活性相关的病症和用于抑制KSP驱动蛋白的氟化氨基烷基-4-氧代-3,4-二氢吡啶并[3,4-d]嘧啶衍生物。 本发明还涉及包含这些化合物的组合物,以及使用它们治疗哺乳动物癌症的方法。