| Literature DB >> 16107159 |
Guo Q Shi1, James F Dropinski, Yong Zhang, Conrad Santini, Soumya P Sahoo, Joel P Berger, Karen L Macnaul, Gaochao Zhou, Arun Agrawal, Raul Alvaro, Tian-Quan Cai, Melba Hernandez, Samuel D Wright, David E Moller, James V Heck, Peter T Meinke.
Abstract
The design and synthesis of a novel class of 2,3-dihydrobenzofuran-2-carboxylic acids as highly potent and subtype-selective PPARalpha agonists are reported. Systematic study of structure-activity relationships has identified several key structural elements within this class for maintaining the potency and subtype selectivity. Select compounds were evaluated in animal models of dyslipidemia using Syrian hamsters and male Beagle dogs, and all these compounds displayed excellent cholesterol- and triglyceride-lowering activity at dose levels that were much lower than the marketed weak PPARalpha agonist fenofibrate.Entities:
Mesh:
Substances:
Year: 2005 PMID: 16107159 DOI: 10.1021/jm050373g
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446