Isoxazoles / O-pyridines with ethyl and ethenyl linker
申请人:Buettelmann Bernd
公开号:US08389550B2
公开(公告)日:2013-03-05
The present invention is concerned with novel isoxazole-pyridines of formula I
wherein R1, R2, R3 and L 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 pharmaceutical agents.
本发明涉及一种新型异噁唑-吡啶化合物,其化学式为I,其中R1、R2、R3和L如所述,以及其药学上可接受的盐和酯。本发明的活性化合物具有亲和力和选择性作用于GABA A α5受体。此外,本发明涉及制备化合物I的活性化合物、含有它们的药物组合物以及它们作为药物剂量的使用。
ISOXAZOLE / O-PYRIDINE DERIVATIVES WITH ETHYL AND ETHENYL LINKER AS GABA A ALPHA5 RECEPTOR INVERSE AGONISTS
申请人:F. Hoffmann-La Roche AG
公开号:EP2401271A1
公开(公告)日:2012-01-04
METHODS AND COMPOSITIONS FOR TREATING A SUBJECT FOR CENTRAL NERVOUS SYSTEM (CNS) INJURY
申请人:The Regents of the University of California
公开号:EP2575455A2
公开(公告)日:2013-04-10
US8389550B2
申请人:——
公开号:US8389550B2
公开(公告)日:2013-03-05
[EN] ISOXAZOLE / O-PYRIDINE DERIVATIVES WITH ETHYL AND ETHENYL LINKER<br/>[FR] DÉRIVÉS ISOXAZOLE / O-PYRIDINE AVEC SÉQUENCE DE LIAISON ÉTHYLE ET ÉTHÉNYLE
申请人:HOFFMANN LA ROCHE
公开号:WO2010097368A1
公开(公告)日:2010-09-02
The present invention is concerned with novel isoxazole-pyridine derivatives of formula I wherein R1, R2, R3 and L 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 medicaments.