Title of article
Design, synthesis, biological evaluation and docking studies of pterostilbene analogs inside PPARα Original Research Article
Author/Authors
Cassia S. Mizuno، نويسنده , , Guoyi Ma، نويسنده , , Shabana Khan، نويسنده , , Akshay Patny، نويسنده , , Mitchell A. Avery، نويسنده , , Agnes M. Rimando، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2008
Pages
9
From page
3800
To page
3808
Abstract
Pterostilbene, a naturally occurring analog of resveratrol, has previously shown PPARα activation in H4IIEC3 cells and was found to decrease cholesterol levels in animals. In this study, analogs of pterostilbene were synthesized and their ability to activate PPARα was investigated. Among analogs that was synthesized (E)-4-(3,5-dimethoxystyryl)phenyl dihydrogen phosphate showed activity higher than pterostilbene and control drug ciprofibrate. Docking of the stilbenes inside PPARα showed the presence of important hydrogen bond interactions for PPARα activation.
Keywords
Resveratrol , Dyslipidemia , Pterostilbene , Peroxisome proliferator activated receptor
Journal title
Bioorganic and Medicinal Chemistry
Serial Year
2008
Journal title
Bioorganic and Medicinal Chemistry
Record number
1304211
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