作者:Anne-Marie Liberatore、Jocelyne Schulz、Jacques Pommier、Marie-Anne Barthelemy、Marion Huchet、Pierre-Etienne Chabrier、Dennis Bigg
DOI:10.1016/j.bmcl.2004.04.059
日期:2004.7
A series of 2-alkyl-4-arylimidazoles were prepared and their binding affinities to the site-2 sodium (Na+) channel were determined. SAR studies led to highly potent Na+ channel blockers. (C) 2004 Elsevier Ltd. All rights reserved.