Inhibitors of 11beta-hydroxysteroid dehydrogenase 1
    48.
    发明授权
    Inhibitors of 11beta-hydroxysteroid dehydrogenase 1 有权
    11β-羟基类固醇脱氢酶抑制剂1

    公开(公告)号:US08846668B2

    公开(公告)日:2014-09-30

    申请号:US13054954

    申请日:2009-07-23

    IPC分类号: A61K31/535 C07D413/00

    CPC分类号: C07D413/10 C07D413/14

    摘要: This invention relates to novel compounds of the Formula (I), (Ia1-10), (Ib1-10), (Ic1-10), (Id1-7), (Ie1-5) pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful for the therapeutic treatment of diseases associated with the modulation or inhibition of 11β-HSD1 in mammals. The invention further relates to pharmaceutical compositions of the novel compounds and methods for their use in the reduction or control of the production of cortisol in a cell or the inhibition of the conversion of cortisone to cortisol in a cell.

    摘要翻译: 本发明涉及式(I),(Ia1-10),(Ib1-10),(Ic1-10),(Id1-7),(Ⅰe1-5)其药学上可接受的盐的新型化合物和药物组合物 其可用于治疗与哺乳动物中11β-HSD1的调节或抑制相关的疾病的治疗。 本发明进一步涉及新化合物的药物组合物及其用于减少或控制细胞中皮质醇产生或抑制细胞中可的松转化为皮质醇的方法。

    INHIBITORS OF 11beta-HYDROXYSTEROID DEHYDROGENASE 1
    49.
    发明申请
    INHIBITORS OF 11beta-HYDROXYSTEROID DEHYDROGENASE 1 有权
    11β-羟基脱氢酶脱氢酶抑制剂1

    公开(公告)号:US20120108578A1

    公开(公告)日:2012-05-03

    申请号:US13054954

    申请日:2009-07-23

    CPC分类号: C07D413/10 C07D413/14

    摘要: This invention relates to novel compounds of the Formula (I), (Ia1-10), (Ib1-10), (Ic1-10), (Id1-7), (Ie1-5) pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof, which are useful for the therapeutic treatment of diseases associated with the modulation or inhibition of 11β-HSD1 in mammals. The invention further relates to pharmaceutical compositions of the novel compounds and methods for their use in the reduction or control of the production of cortisol in a cell or the inhibition of the conversion of cortisone to cortisol in a cell.

    摘要翻译: 本发明涉及式(I),(Ia1-10),(Ib1-10),(Ic1-10),(Id1-7),(Ⅰe1-5)其药学上可接受的盐的新型化合物和药物组合物 其可用于治疗与哺乳动物中11β-HSD1的调节或抑制相关的疾病的治疗。 本发明进一步涉及新化合物的药物组合物及其用于减少或控制细胞中皮质醇产生或抑制细胞中可的松转化为皮质醇的方法。