Compositions Useful as Inhibitors of Protein Kinases
    43.
    发明申请
    Compositions Useful as Inhibitors of Protein Kinases 失效
    可用作蛋白激酶抑制剂的组合物

    公开(公告)号:US20090325968A1

    公开(公告)日:2009-12-31

    申请号:US12552003

    申请日:2009-09-01

    CPC分类号: C07D487/04

    摘要: The present invention provides a compound of formula I: or a pharmaceutically acceptable salt or mixtures thereof. These compounds are inhibitors of protein kinases, particularly inhibitors of GSK mammalian protein kinase, and more particularly inhibitors of GSK-3 mammalian protein kinase. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of utilizing those compounds and compositions in the treatment of various protein kinase mediated disorders.

    摘要翻译: 本发明提供式I化合物或其药学上可接受的盐或其混合物。 这些化合物是蛋白激酶的抑制剂,特别是GSK哺乳动物蛋白激酶的抑制剂,特别是GSK-3哺乳动物蛋白激酶的抑制剂。 本发明还提供包含本发明化合物的药学上可接受的组合物和利用这些化合物和组合物治疗各种蛋白激酶介导的病症的方法。

    Target ligand generation
    49.
    发明授权
    Target ligand generation 有权
    靶配体生成

    公开(公告)号:US07716030B2

    公开(公告)日:2010-05-11

    申请号:US10790507

    申请日:2004-03-01

    IPC分类号: G06G7/58 G01N33/48

    摘要: Methods of identifying potential ligands for macromolecular targets are disclosed herein. The methods comprise providing models of three dimensional structural information for ligands or a ligand:macromolecule complex, mapping spatial relationships between the models, and identifying one or more pairs of matching bonds. Databases and apparatuses are also provided.

    摘要翻译: 本文公开了鉴定大分子靶标潜在配体的方法。 所述方法包括提供配体或配体:大分子复合物的三维结构信息模型,绘制模型之间的空间关系,以及鉴定一对或多对匹配键。 还提供了数据库和设备。