Synthesis and structure-activity relationships of a novel series of 2,3,5,6,7,9-hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide K(ATP) channel openers: discovery of (-)-(9S)-9-(3-bromo-4-fluorophenyl)-2,3,5,6,7,9- hexahydrothieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide (A-278637), a potent K(ATP) opener that selectively inhibits spontaneous bladder contractions.

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Published in J Med Chem on June 03, 2004

Authors

William A Carroll1, Robert J Altenbach, Hao Bai, Jorge D Brioni, Michael E Brune, Steven A Buckner, Christopher Cassidy, Yiyuan Chen, Michael J Coghlan, Anthony V Daza, Irene Drizin, Thomas A Fey, Michael Fitzgerald, Murali Gopalakrishnan, Robert J Gregg, Rodger F Henry, Mark W Holladay, Linda L King, Michael E Kort, Philip R Kym, Ivan Milicic, Rui Tang, Sean C Turner, Kristi L Whiteaker, Lin Yi, Henry Zhang, James P Sullivan

Author Affiliations

1: Abbott Laboratories, Neuroscience Research, Global Pharmaceutical Research and Development, Abbott Park, IL 60064-6101, USA. william.a.carroll@abbott.com

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