Structure–activity relationship of a novel class of naphthyl amide KATP channel openers
作者:Sean C Turner、William A Carroll、Tammie K White、Michael E Brune、Steven A Buckner、Murali Gopalakrishnan、Adebola Fabiyi、Michael J Coghlan、Victoria E Scott、Neil A Castle、Anthony V Daza、Ivan Milicic、James P Sullivan
DOI:10.1016/s0960-894x(03)00205-1
日期:2003.5
We have discovered a novel series of N-[2-(2,2,2-trifluoro-1-hydroxy-1-trifluoromethyl-ethyl)-naphthalen-1-yl] amides that are potent openers of K-ATP channels and investigated structure-activity relationships (SAR) around the 1,2-disubstituted naphthyl core. A-151892, a prototype compound of this series, was found to be a potent and efficacious potassium channel opener in vitro in transfected Kir6.2/SUR2B cells and pig bladder strips. Additionally, A-151892 was found to selectively inhibit unstable bladder contractions in vivo in an obstructed rat model of myogenic bladder function. (C) 2003 Elsevier Science Ltd. All rights reserved.
Naphthalene amides as potassium channel openers
申请人:——
公开号:US20030199578A1
公开(公告)日:2003-10-23
The present invention relates to compounds and their ability to act as potassium channel openers.