1007112-35-7Relevant academic research and scientific papers
Discovery of 2-substituted benzoxazole carboxamides as 5-HT3 receptor antagonists
Yang, Zhicai,Fairfax, David J.,Maeng, Jun-Ho,Masih, Liaqat,Usyatinsky, Alexander,Hassler, Carla,Isaacson, Soshanna,Fitzpatrick, Kevin,Deorazio, Russell J.,Chen, Jianqing,Harding, James P.,Isherwood, Matthew,Dobritsa, Svetlana,Christensen, Kevin L.,Wierschke, Jonathan D.,Bliss, Brian I.,Peterson, Lisa H.,Beer, Cathy M.,Cioffi, Christopher,Lynch, Michael,Rennells, W. Martin,Richards, Justin J.,Rust, Timothy,Khmelnitsky, Yuri L.,Cohen, Marlene L.,Manning, David D.
scheme or table, p. 6538 - 6541 (2010/11/21)
A new class of 2-substituted benzoxazole carboxamides are presented as potent functional 5-HT3 receptor antagonists. The chemical series possesses nanomolar in vitro activity against human 5-HT3A receptors. A chemistry optimization program was conducted and identified 2-aminobenzoxazoles as orally active 5-HT3 receptor antagonists with good metabolic stability. These novel analogues possess drug-like characteristics and have potential utility for the treatment of diseases attributable to improper 5-HT3 receptor function, especially diarrhea predominant irritable bowel syndrome (IBS-D).
2-AMINOBENZOXAZOLE CARBOXAMIDES AS 5HT3 MODULATORS
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Page/Page column 7, (2008/12/04)
Compounds of formulae I, II and III: are disclosed as 5-HT3 inhibitors. The compounds are useful in treating CINV, IBS-D and other diseases and conditions.
BENZOOXAZOLE, OXAZOLOPYRIDINE, BENZOTHIAZOLE AND THIAZOLOPYRIDINE DERIVATIVES
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Page/Page column 79, (2008/06/13)
This invention is concerned with compounds of the formula (I) wherein X, A, B, R1, R2 and G are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The invention further relates to pharmaceutical
