Synthesis and characterization of 8-ethynyl-1,3-dihydro-benzo[b][1,4]diazepin-2-one derivatives: New potent non-competitive metabotropic glutamate receptor 2/3 antagonists. Part 1
作者:Thomas J. Woltering、Geo Adam、Alexander Alanine、Jürgen Wichmann、Frédéric Knoflach、Vincent Mutel、Silvia Gatti
DOI:10.1016/j.bmcl.2007.10.026
日期:2007.12
A series of 1,3-dihydro-benzo[b][1,4]diazepin-2-one derivatives was evaluated as non-competitive mGluR2/3 antagonists. Attachment of an 8-(2-aryl)-ethynyl-moiety produced compounds inhibiting the binding of [H-3]-LY354740 to rat mGluR2 with low nanomolar affinity and consistent functional effect at both mGIuR2 and mGluR3. (c) 2007 Elsevier Ltd. All rights reserved.
CLEANING COMPOSITIONS AND TABLETS
申请人:THE PROCTER & GAMBLE COMPANY
公开号:EP1175477A1
公开(公告)日:2002-01-30
BENZODIAZEPINE DERIVATIVES AS METABOTROPIC GLUTAMATE RECEPTOR ANTAGONISTS