Synthesis and structure–activity relationships of 2-(1,4′-bipiperidin-1′-yl)thiazolopyridine as H3 receptor antagonists
作者:Ashwin U. Rao、Anandan Palani、Xiao Chen、Ying Huang、Robert G. Aslanian、Robert E. West、Shirley M. Williams、Ren-Long Wu、Joyce Hwa、Christopher Sondey、Jean Lachowicz
DOI:10.1016/j.bmcl.2009.09.006
日期:2009.11
A series of 2-(1,4′-bipiperidine-1′-yl)thiazolopyridines was synthesized and evaluated as a new lead of non-imidazole histamine H3 receptor antagonists. Introduction of diversity at the 6-position of the pyridine ring was designed to enhance in vitro potency and decrease hERG activity. The structure–activity relationships for these new thiazolopyridine antagonists are discussed.
Bicyclic Heterocyclic Derivatives and Methods of Use Thereof
申请人:Palani Anandan
公开号:US20110319434A1
公开(公告)日:2011-12-29
The present invention relates to novel Bicyclic Heterocyclic Derivatives, pharmaceutical compositions comprising the Bicyclic Heterocyclic Derivatives and the use of these compounds for treating or preventing treating allergy, an allergy-induced airway response, congestion, a cardiovascular disease, an inflammatory disease, a gastrointestinal disorder, a neurological disorder, a cognitive disorder, a metabolic disorder, obesity or an obesity-related disorder, diabetes, a diabetic complication, impaired glucose tolerance or impaired fasting glucose.