Discovery of novel modulators of metabotropic glutamate receptor subtype-5
摘要:
A series of potent and selective mGluR5 antagonists were synthesized and evaluated in vitro and in vivo. It was found that a pyridyl functionality is a potential replacement for acetonitrile in the lead structure, with 2-pyridyl being most favored. Additionally, the benzoxazole moiety could also be replaced by other heterobicyclic rings such as imidazothiazole. (C) 2003 Elsevier Ltd. All rights reserved.
[EN] FUSED HETEROBICYCLO SUBSTITUTED PHENYL METABOTROPIC GLUTAMATE-5 MODULATORS<br/>[FR] MODULATEURS DU RECEPTEUR GLUTAMATE METABOTROPIQUE 5 (MGLUR5) DE PHENYLE SUBSTITUES PAR UN FRAGMENT HETEROBICYCLO FUSIONNE
申请人:MERCK & CO INC
公开号:WO2004024074A2
公开(公告)日:2004-03-25
Phenyl compounds substituted with a fused-heterobicyclo moiety, are mGluR5 modulators useful in the treatment of psychiatric and mood disorders such as, for example, schizophrenia, anxiety, depression, and panic, as well as in the treatment of pain and other diseases.
Discovery of novel modulators of metabotropic glutamate receptor subtype-5
作者:Bowei Wang、Jean-Michel Vernier、Sara Rao、Janice Chung、Jeffery J Anderson、Jesse D Brodkin、Xiaohui Jiang、Michael F Gardner、Xiaoqing Yang、Benito Munoz
DOI:10.1016/j.bmc.2003.10.021
日期:2004.1
A series of potent and selective mGluR5 antagonists were synthesized and evaluated in vitro and in vivo. It was found that a pyridyl functionality is a potential replacement for acetonitrile in the lead structure, with 2-pyridyl being most favored. Additionally, the benzoxazole moiety could also be replaced by other heterobicyclic rings such as imidazothiazole. (C) 2003 Elsevier Ltd. All rights reserved.