کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1371053 | 981838 | 2011 | 5 صفحه PDF | دانلود رایگان |
A novel series of oxime containing benzyl-1,3-dioxane-r-2-carboxylic acid derivatives (6a–k) were designed as selective PPARα agonists, through bioisosteric modification in the lipophilic tail region of PPARα/γ dual agonist. Some of the test compounds (6a, 6b, 6c and 6f) showed high selectivity towards PPARα over PPARγ in vitro. Further, highly potent and selective PPARα agonist 6c exhibited significant antihyperglycemic and antihyperlipidemic activity in vivo, along with its improved pharmacokinetic profile. Favorable in-silico interaction of 6c with PPARα binding pocket correlate its in vitro selectivity profile toward PPARα over PPARγ. Together, these results confirm discovery of novel series of oxime based selective PPARα agonists for the safe and effective treatment of various metabolic disorders.
A novel series of oxime containing benzyl-1,3-dioxane-r-2-carboxylic acid derivatives are reported as selective PPARα agonists. Some of the test compounds exhibited good selectivity towards PPARα over PPARγ in vitro and the lead compound 6c showed excellent antihyperglycemic and antihyperlipidemic activity in vivo.Figure optionsDownload as PowerPoint slide
Journal: Bioorganic & Medicinal Chemistry Letters - Volume 21, Issue 2, 15 January 2011, Pages 628–632