Discovery of {4-[4,9-bis(ethyloxy)-1-oxo-1,3-dihydro-2H-benzo[f]isoindol-2-yl]-2-fluorophenyl}acetic acid (GSK726701A), a novel EP4 receptor partial agonist for the treatment of pain
摘要:
A novel series of EP4 agonists and antagonists have been identified, and then used to validate their potential in the treatment of inflammatory pain. This paper describes these novel ligands and their activity within a number of pre-chmcal models of pain, ultimately leading to the identification of the EP4 partial agonist GSK726701A. (C) 2018 Elsevier Ltd. All rights reserved.
The present invention relates to indole derivatives, to processes for their preparation, to pharmaceutical compositions containing them and to their use in medicine.
[EN] ISOINDOL DERIVATIVES AS EP4 RECEPTOR AGONISTS<br/>[FR] DÉRIVÉS D'ISO-INDOLE EN TANT QU'AGONISTES DES RÉCEPTEURS EP4
申请人:GLAXO GROUP LTD
公开号:WO2008046798A1
公开(公告)日:2008-04-24
[EN] The present invention relates to indole derivatives, to processes for their preparation, to pharmaceutical compositions containing them and to their use in medicine. [FR] La présente invention concerne des dérivés d'indole, leurs procédés de préparation, des compositions pharmaceutiques les contenant et leurs applications médicales.