Pyridines
    1.
    发明授权
    Pyridines 有权
    吡啶类

    公开(公告)号:US08415379B2

    公开(公告)日:2013-04-09

    申请号:US12768762

    申请日:2010-04-28

    IPC分类号: A61K31/443 C07D413/14

    摘要: The present invention is concerned with isoxazole-pyridines of formula I, having affinity and selectivity for GABA A α5 receptor, their manufacture, pharmaceutical compositions containing them and their use as pharmaceuticals. The active compounds of the present invention are useful as cognitive enhancer or for the therapeutic and/or prophylactic treatment of cognitive disorders like Alzheimer's disease.

    摘要翻译: 本发明涉及式I的异恶唑 - 吡啶,对GABA Aα5受体具有亲和性和选择性,其制备方法,含有它们的药物组合物及其作为药物的用途。 本发明的活性化合物可用作认知增强剂或用于治疗和/或预防性治疗认知障碍如阿尔茨海默氏病。

    Pyridines
    2.
    发明授权
    Pyridines 有权
    吡啶类

    公开(公告)号:US08357703B2

    公开(公告)日:2013-01-22

    申请号:US12772250

    申请日:2010-05-03

    IPC分类号: A61K31/4427 C07D413/12

    CPC分类号: C07D413/12 C07D413/14

    摘要: The present invention is concerned with novel isoxazoles of formula I wherein X, R1, R2, R3 and R4 are as described herein, as well as pharmaceutically acceptable salts and esters thereof. The active compounds of the present invention have affinity and selectivity for GABA A α5 receptor. Further the present invention is concerned with the manufacture of the active compounds of formula I, pharmaceutical compositions containing them and their use as therapeutics.

    摘要翻译: 本发明涉及式I的新异恶唑,其中X,R 1,R 2,R 3和R 4如本文所述,以及其药学上可接受的盐和酯。 本发明的活性化合物对GABA Aα5受体具有亲和性和选择性。 此外,本发明涉及制备式I的活性化合物,含有它们的药物组合物及其作为治疗剂的用途。

    Thiazoles
    3.
    发明授权
    Thiazoles 有权
    噻唑

    公开(公告)号:US08178522B2

    公开(公告)日:2012-05-15

    申请号:US12768779

    申请日:2010-04-28

    摘要: The present invention is concerned with isoxazole-thiazole derivatives of formula I, having affinity and selectivity for GABA A α5 receptor, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful as cognitive enhancer or for the therapeutic and/or prophylactic treatment of cognitive disorders like Alzheimer's disease.

    摘要翻译: 本发明涉及式I的异恶唑 - 噻唑衍生物,其具有对GABA Aα5受体的亲和性和选择性,它们的制备,含有它们的药物组合物及其作为治疗活性物质的用途。 本发明的活性化合物可用作认知增强剂或用于治疗和/或预防性治疗认知障碍如阿尔茨海默氏病。

    THIAZOLES
    4.
    发明申请

    公开(公告)号:US20100286116A1

    公开(公告)日:2010-11-11

    申请号:US12768779

    申请日:2010-04-28

    摘要: The present invention is concerned with isoxazole-thiazole derivatives of formula I, having affinity and selectivity for GABA A α5 receptor, their manufacture, pharmaceutical compositions containing them and their use as therapeutically active substances. The active compounds of the present invention are useful as cognitive enhancer or for the therapeutic and/or prophylactic treatment of cognitive disorders like Alzheimer's disease.

    摘要翻译: 本发明涉及式I的异恶唑 - 噻唑衍生物,其具有对GABA Aα5受体的亲和性和选择性,它们的制备,含有它们的药物组合物及其作为治疗活性物质的用途。 本发明的活性化合物可用作认知增强剂或用于治疗和/或预防性治疗认知障碍如阿尔茨海默氏病。

    ISOXAZOLES
    8.
    发明申请
    ISOXAZOLES 审中-公开

    公开(公告)号:US20100280019A1

    公开(公告)日:2010-11-04

    申请号:US12766125

    申请日:2010-04-23

    CPC分类号: C07D413/12 C07D413/14

    摘要: The present invention is concerned with novel isoxazole derivatives of formula I wherein X, R1, R2, R3, R4 and R5 are as described herein, as well as pharmaceutically acceptable salts and esters thereof. The active compounds of the present invention have affinity and selectivity for GABA A α5 receptor. Further the present invention is concerned with the manufacture of the active compounds of formula I, pharmaceutical compositions containing them and their use as pharmaceuticals.

    摘要翻译: 本发明涉及式I的新型异恶唑衍生物,其中X,R 1,R 2,R 3,R 4和R 5如本文所述,以及其药学上可接受的盐和酯。 本发明的活性化合物对GABA Aα5受体具有亲和性和选择性。 此外,本发明涉及制备式I的活性化合物,含有它们的药物组合物及其作为药物的用途。

    Isoxazoles
    9.
    发明授权
    Isoxazoles 有权
    异恶唑

    公开(公告)号:US08227461B2

    公开(公告)日:2012-07-24

    申请号:US12766202

    申请日:2010-04-23

    CPC分类号: C07D413/12 C07D413/14

    摘要: The present invention is concerned with novel isoxazole derivatives of formula I wherein X, R1, R2, R3, R4 and R5 are as described herein, as well as pharmaceutically acceptable salts and esters thereof. The active compounds of the present invention have affinity and selectivity for GABA A α5 receptor. Further the present invention is concerned with the manufacture of the active compounds of formula I, pharmaceutical compositions containing them and their use as pharmaceuticals.

    摘要翻译: 本发明涉及式I的新型异恶唑衍生物,其中X,R 1,R 2,R 3,R 4和R 5如本文所述,以及其药学上可接受的盐和酯。 本发明的活性化合物对GABA Aα5受体具有亲和性和选择性。 此外,本发明涉及制备式I的活性化合物,含有它们的药物组合物及其作为药物的用途。