1. Academic Validation
  2. Pharmacophore-driven identification of PPARγ agonists from natural sources

Pharmacophore-driven identification of PPARγ agonists from natural sources

  • J Comput Aided Mol Des. 2011 Feb;25(2):107-16. doi: 10.1007/s10822-010-9398-5.
Rasmus K Petersen 1 Kathrine B Christensen Andreana N Assimopoulou Xavier Fretté Vassilios P Papageorgiou Karsten Kristiansen Irene Kouskoumvekaki
Affiliations

Affiliation

  • 1 Department of Biology, University of Copenhagen, Ole Maaløes Vej 5, 2200 Copenhagen, Denmark.
Abstract

In a search for more effective and safe anti-diabetic compounds, we developed a pharmacophore model based on partial agonists of PPARγ. The model was used for the virtual screening of the Chinese Natural Product Database (CNPD), a library of plant-derived Natural Products primarily used in folk medicine. From the resulting hits, we selected methyl oleanonate, a compound found, among Others, in Pistacia lentiscus var. Chia oleoresin (Chios mastic gum). The acid of methyl oleanonate, oleanonic acid, was identified as a PPARγ Agonist through bioassay-guided chromatographic fractionations of Chios mastic gum fractions, whereas some other sub-fractions exhibited also biological activity towards PPARγ. The results from the present work are two-fold: on the one hand we demonstrate that the pharmacophore model we developed is able to select novel ligand scaffolds that act as PPARγ agonists; while at the same time it manifests that Natural Products are highly relevant for use in virtual screening-based drug discovery.

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