POLYMORPHS AND SALTS OF A KINASE INHIBITOR
    1.
    发明申请
    POLYMORPHS AND SALTS OF A KINASE INHIBITOR 有权
    激酶抑制剂的多聚体和盐

    公开(公告)号:US20110160240A1

    公开(公告)日:2011-06-30

    申请号:US12952879

    申请日:2010-11-23

    CPC分类号: A61K31/54 C07D471/04

    摘要: The present invention relates to novel crystalline polymorphic salt forms of 5-(3-chlorophenylamino)benzo[c][2,6]naphthyridine-8-carboxylic acid, processes for the preparation thereof, compositions thereof and their use in methods of treatment and prevention of conditions mediated by casein kinase (CK) and/or poly(ADP-ribose)polymerase (PARD).

    摘要翻译: 本发明涉及5-(3-氯苯基氨基)苯并[c] [2,6]萘啶-8-羧酸的新型结晶多晶型盐形式,其制备方法,组合物及其在治疗方法中的应用 预防由酪蛋白激酶(CK)和/或聚(ADP-核糖)聚合酶(PARD)介导的病症。

    Polymorphs and salts of a kinase inhibitor
    6.
    发明授权
    Polymorphs and salts of a kinase inhibitor 有权
    激酶抑制剂的多晶型物和盐

    公开(公告)号:US08853235B2

    公开(公告)日:2014-10-07

    申请号:US12952879

    申请日:2010-11-23

    CPC分类号: A61K31/54 C07D471/04

    摘要: The present invention relates to novel crystalline polymorphic salt forms of 5-(3-chlorophenylamino)benzo[c][2,6]naphthyridine-8-carboxylic acid, processes for the preparation thereof, compositions thereof and their use in methods of treatment and prevention of conditions mediated by casein kinase (CK) and/or poly(ADP-ribose)polymerase (PARP).

    摘要翻译: 本发明涉及5-(3-氯苯基氨基)苯并[c] [2,6]萘啶-8-羧酸的新型结晶多晶型盐形式,其制备方法,组合物及其在治疗方法中的应用 预防由酪蛋白激酶(CK)和/或聚(ADP-核糖)聚合酶(PARP)介导的病症。

    DEUTERATED SERINE-THREONINE PROTEIN KINASE MODULATORS
    9.
    发明申请
    DEUTERATED SERINE-THREONINE PROTEIN KINASE MODULATORS 审中-公开
    DEUTERATED丝氨酸蛋白激酶激酶调节剂

    公开(公告)号:US20120129849A1

    公开(公告)日:2012-05-24

    申请号:US13242525

    申请日:2011-09-23

    CPC分类号: A61K31/44

    摘要: The present invention provides deuterated compounds having certain biological activities that include, but are not limited to, inhibiting cell proliferation, modulating protein kinase activity and modulating polymerase activity. The deuterated compounds of the invention can modulate casein kinase (CK) activity and/or poly(ADP-ribose)polymerase (PARP) activity. The invention also relates in part to methods for using such deuterated compounds as therapeutic agents.

    摘要翻译: 本发明提供具有某些生物学活性的氘化化合物,其包括但不限于抑制细胞增殖,调节蛋白激酶活性和调节聚合酶活性。 本发明的氘代化合物可以调节酪蛋白激酶(CK)活性和/或聚(ADP-核糖)聚合酶(PARP)活性。 本发明还部分涉及使用这种氘代化合物作为治疗剂的方法。