Substituted bicyclolactam compounds
    4.
    发明授权
    Substituted bicyclolactam compounds 失效
    取代的双环内酰胺化合物

    公开(公告)号:US07718645B2

    公开(公告)日:2010-05-18

    申请号:US12357544

    申请日:2009-01-22

    CPC分类号: C07D498/04

    摘要: The invention provides compounds of formula (1), and the pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R4, R5a, R5b, R5c, R5d, Q, A, Z, and R7 are as described herein; compositions thereof; and uses thereof.

    摘要翻译: 本发明提供式(1)化合物及其药学上可接受的盐,其中R1,R2,R3,R4,R5a,R5b,R5c,R5d,Q,A,Z和R7如本文所述; 组合物; 及其用途。

    Substituted Bicyclolactam Compounds
    5.
    发明申请
    Substituted Bicyclolactam Compounds 失效
    取代的双环内酰胺化合物

    公开(公告)号:US20090137551A1

    公开(公告)日:2009-05-28

    申请号:US12357544

    申请日:2009-01-22

    CPC分类号: C07D498/04

    摘要: The invention provides compounds of formula (1), and the pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R4, R5a, R5b, R5c, R5d, Q, A, Z, and R7 are as described herein; compositions thereof; and uses thereof.

    摘要翻译: 本发明提供式(1)化合物及其药学上可接受的盐,其中R1,R2,R3,R4,R5a,R5b,R5c,R5d,Q,A,Z和R7如本文所述; 组合物; 及其用途。

    SUBSTITUTED BICYCLOLACTAM COMPOUNDS
    6.
    发明申请
    SUBSTITUTED BICYCLOLACTAM COMPOUNDS 审中-公开
    取代的双氰胺化合物

    公开(公告)号:US20090036425A1

    公开(公告)日:2009-02-05

    申请号:US12174820

    申请日:2008-07-17

    CPC分类号: C07D498/04

    摘要: The invention provides compounds of formula (1), and the pharmaceutically acceptable salt thereof, wherein R1, R2, R3, R4, R5a, R5b, R5c, R5d, Q, A, Z, and R7 are as described herein; compositions thereof; and uses thereof.

    摘要翻译: 本发明提供式(1)化合物及其药学上可接受的盐,其中R1,R2,R3,R4,R5a,R5b,R5c,R5d,Q,A,Z和R7如本文所述; 组合物; 及其用途。

    Heterocyclic .beta.-adrenergic agonists
    10.
    发明授权
    Heterocyclic .beta.-adrenergic agonists 失效
    杂环β-肾上腺素能激动剂

    公开(公告)号:US5843972A

    公开(公告)日:1998-12-01

    申请号:US827289

    申请日:1997-03-28

    摘要: The present invention relates to certain compounds of the formula (I) the racemic-enantiomeric mixtures and optical isomers of said compounds and the pharmaceutically acceptable salts or prodrugs thereof, depicted below, which are .beta.-adrenergic receptor agonists and accordingly have utility as, inter alia, hypoglycemic and antiobesity agents. More specifically, the compounds of the instant invention are selective agonists of .beta..sub.3 -adrenergic receptor. The invention also relates to methods of use for the compounds and to pharmaceutical compositions containing them. The compounds of the present invention also possess utility for increasing lean meat deposition and/or improving the lean meat to fat ratio in animals, e.g., ungulate animals, companion animals and poultry. The compounds have the formula ##STR1## wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, Y and Z are as defined in the specification.

    摘要翻译: 本发明涉及某些式(I)化合物,所述化合物的外消旋对映异构体混合物和光学异构体及其药学上可接受的盐或前药如下所述,其为β-肾上腺素能受体激动剂,因此具有效用 尤其是低血糖和抗肥胖剂。 更具体地,本发明的化合物是β3肾上腺素能受体的选择性激动剂。 本发明还涉及用于化合物的方法和含有它们的药物组合物。 本发明的化合物还具有用于增加动物,例如有蹄动物,伴侣动物和家禽的瘦肉沉积和/或改善瘦肉与脂肪比的效用。 化合物具有式(I)其中R 1,R 2,R 3,R 4,R 5,Y和Z如说明书中所定义。