α1-Adrenoceptor Agonists: The Identification of Novel α1A Subtype Selective 2′-Heteroaryl-2-(phenoxymethyl)imidazolines
摘要:
Novel 2'-heteroaryl-2-(phenoxymethyl)imidazolines have been identified as potent agonists of the cloned human alpha(1)-adrenoceptors in vitro. The nature of the 2'-heteroaryl group can have significant effects on the potency, efficacy, and subtype selectivity in this series. alpha(1A) Subtype selective agonists have been identified. (C) 2002 Elsevier Science Ltd. All rights reserved.
THIENOPYRIMIDINES USEFUL AS MODULATORS OF ION CHANNELS
申请人:Vertex Pharmaceuticals, Inc.
公开号:EP2043654A2
公开(公告)日:2009-04-08
[EN] THIENOPYRIMIDINES USEFUL AS MODULATORS OF ION CHANNELS<br/>[FR] THIÉNOPYRIMIDINES UTILES EN TANT QUE MODULATEURS DE CANAUX IONIQUES
申请人:VERTEX PHARMA
公开号:WO2007146284A2
公开(公告)日:2007-12-21
[EN] The present invention relates to compounds useful as inhibitors of ion channels. The invention also provides pharmaceutically acceptable compositions comprising the compounds of the invention and methods of using the compositions in the treatment of various disorders. [FR] La présente invention concerne des composés utiles en tant qu'inhibiteurs de canaux ioniques. L'invention concerne en outre des compositions pharmaceutiquement acceptables comprenant les composés de l'invention et des procédés d'utilisation des compositions dans le traitement de différents troubles.