Novel pyrazolopyridines as cyclin dependent kinase inhibitors
    4.
    发明申请
    Novel pyrazolopyridines as cyclin dependent kinase inhibitors 有权
    新型吡唑并吡啶类作为细胞周期蛋白依赖性激酶抑制剂

    公开(公告)号:US20040097516A1

    公开(公告)日:2004-05-20

    申请号:US10664337

    申请日:2003-09-17

    CPC分类号: C07D471/04

    摘要: In its many embodiments, the present invention provides a novel class of pyrazolonull1,5-anullpyridine compounds as inhibitors of cyclin dependent kinases, methods of preparing such compounds, pharmaceutical compositions containing one or more such compounds, methods of preparing pharmaceutical formulations comprising one or more such compounds, and methods of treatment, prevention, inhibition, or amelioration of one or more diseases associated with the CDKs using such compounds or pharmaceutical compositions.

    摘要翻译: 在其许多实施方案中,本发明提供了一类新颖的吡唑并[1,5-a]吡啶化合物作为细胞周期蛋白依赖性激酶的抑制剂,制备此类化合物的方法,含有一种或多种此类化合物的药物组合物,制备药物制剂的方法 包括一种或多种这样的化合物,以及使用这些化合物或药物组合物治疗,预防,抑制或改善与CDK相关的一种或多种疾病的方法。

    Muscarinic antagonists
    7.
    发明申请
    Muscarinic antagonists 失效
    毒蕈碱拮抗剂

    公开(公告)号:US20040067972A1

    公开(公告)日:2004-04-08

    申请号:US10425376

    申请日:2003-04-28

    IPC分类号: A61K031/4747 C07D471/12

    CPC分类号: C07D221/20 C07D211/96

    摘要: The invention described herein are compounds in accordance with formula I: 1 wherein R1, R2, R3, R4, R5, R6, R2, R8, R9, n, X, and Z are as defined herein, pharmaceutical compositions containing at least one compound of formula I, methods of preparation thereof, and methods of treating disorders with at least one compound of formula I or at least one compound of formula I in association with at least one acetylcholinesterase inhibitor.

    摘要翻译: 本文所述的本发明是根据式I的化合物:其中R 1,R 2,R 3,R 4,R 5,R 6,R 2, 8,R 9,n,X和Z如本文所定义,含有至少一种式I化合物的药物组合物,其制备方法,以及用至少一种式I化合物治疗病症的方法或 至少一种式I化合物与至少一种乙酰胆碱酯酶抑制剂联合。