PYRAZOLO[1,5-A][1,3,5]TRIAZINE DERIVATIVES AS CANNABINOID RECEPTOR LIGANDS
申请人:Pfizer Products Inc.
公开号:EP1592691A1
公开(公告)日:2005-11-09
US7329658B2
申请人:——
公开号:US7329658B2
公开(公告)日:2008-02-12
[EN] PYRAZOLO`1,5-A!`1,3,5!TRIAZINE DERIVATIVES AS CANNABINOID RECEPTOR LIGANDS<br/>[FR] DERIVES DE PYRAZOLO[1,5-A][1,3,5]TRIAZINE EN TANT QUE LIGANDS DE RECEPTEUR CANNABINOIDE
申请人:PFIZER PROD INC
公开号:WO2004069837A1
公开(公告)日:2004-08-19
Compounds of Formula (I) that act as cannabinoid receptor ligands and their uses in the treatment of diseases linked to the mediation of the cannabinoid receptors in animals are described herein.
[EN] METHODS FOR IDENTIFYING MODULATORS OF CB1 AND CB2 CANNABINOID RECEPTORS AND THEIR USE IN WOUND HEALING<br/>[FR] PROCEDES PERMETTANT D'IDENTIFIER DES MODULATEURS DES RECEPTEURS CANNABINOIDES CB1 ET CB2 ET LEUR UTILISATION DANS LA CICATRISATION DES BLESSURES
申请人:LIFE & BRAIN GMBH
公开号:WO2006111424A1
公开(公告)日:2006-10-26
[EN] The present invention relates to methods of screening for compounds that modulate the expression of the cannabinoid CBl and CB2 receptors, and methods for modulating receptor activity. The invention also relates to the use of CB 1 and CB2 receptors and/or binding partners for identification of pharmacologically active agents, and their use for enhancing wound healing and treating wound healing disorders. [FR] L'invention concerne des méthodes de criblage de composés qui modulent l'expression des récepteurs cannabinoïdes CB1 et CB2 et des méthodes permettant de moduler l'activité des récepteurs. L'invention concerne également l'utilisation des récepteurs CB1 et CB2 et/ou des partenaires de liaison pour l'identification d'agents actifs sur le plan pharmacologique et leur utilisation pour améliorer la cicatrisation des blessures et le traitement des troubles de la cicatrisation.
Cannabinoid receptor ligands and uses thereof
申请人:Pfizer Inc
公开号:US20040157839A1
公开(公告)日:2004-08-12
Compounds of Formula (I) that act as cannabinoid receptor ligands and their uses in the treatment of diseases linked to the mediation of the cannabinoid receptors in animals are described herein.
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