Pyrrole Derivatives as Alpha 7 NACHR Modulators
    1.
    发明申请
    Pyrrole Derivatives as Alpha 7 NACHR Modulators 有权
    吡咯衍生物作为Alpha 7 NACHR调制器

    公开(公告)号:US20150344422A1

    公开(公告)日:2015-12-03

    申请号:US14655476

    申请日:2014-03-12

    申请人: LUPIN LIMITED

    摘要: Disclosed are compounds of the Formula (I), wherein R1, R2, R3, R4, R5, R6, R7 and m are as described herein, as modulators of the nicotinic acetylcholine receptors, particularly the α7 subtype, their tautomeric forms, stereoisomers, and their pharmaceutically acceptable salts, pharmaceutical compositions thereof, and combinations thereof with suitable other medicaments. Also disclosed are a process of preparation of the compounds and the intended uses thereof in therapy, particularly in the prophylaxis and/or treatment of disorders such as Alzheimer's disease, mild cognitive impairment, and senile dementia.

    摘要翻译: 公开了式(I)的化合物,其中R 1,R 2,R 3,R 4,R 5,R 6,R 7和m如本文所述,作为烟碱乙酰胆碱受体的调节剂,特别是α7亚型,其互变异构体形式,立体异构体, 及其药学上可接受的盐,药物组合物及其与合适的其它药物的组合。 还公开了化合物的制备方法及其在治疗中的预期用途,特别是在诸如阿尔茨海默氏病,轻度认知障碍和老年痴呆症的疾病的预防和/或治疗中。

    Pyrrole Derivatives as Alpha 7 nAChR Modulators
    2.
    发明申请
    Pyrrole Derivatives as Alpha 7 nAChR Modulators 有权
    吡咯衍生物作为Alpha 7 nAChR调制剂

    公开(公告)号:US20160137600A1

    公开(公告)日:2016-05-19

    申请号:US14898773

    申请日:2014-06-16

    申请人: LUPIN LIMITED

    摘要: Disclosed are compounds of the formula (I), wherein R1, R2, R3, R4, R5, R6, R7 and m are as described herein, as modulators of the nicotinic acetylcholine receptors, particularly the α7 subtype, their tautomeric forms, stereoisomers, and their pharmaceutically acceptable salts, pharmaceutical compositions thereof, and combinations thereof with suitable other medicaments. Also disclosed are a process of preparation of the compounds and the intended uses thereof in therapy, particularly in the prophylaxis and/or treatment of disorders such as Alzheimer's disease, mild cognitive impairment, and senile dementia.

    摘要翻译: 公开了式(I)的化合物,其中R1,R2,R3,R4,R5,R6,R7和m如本文所述,作为烟碱乙酰胆碱受体的调节剂,特别是α7亚型,其互变异构体形式,立体异构体, 及其药学上可接受的盐,药物组合物及其与合适的其它药物的组合。 还公开了化合物的制备方法及其在治疗中的预期用途,特别是在诸如阿尔茨海默氏病,轻度认知障碍和老年痴呆症的疾病的预防和/或治疗中。