Literature DB >> 18031621

Structure-based drug design of a novel family of chalcones as PPARalpha agonists: virtual screening, synthesis, and biological activities in vitro.

Xiang-hua Li1, Han-jun Zou, An-hui Wu, Yang-liang Ye, Jian-hua Shen.   

Abstract

AIM: To design and synthesize a novel class of peroxisome proliferator-activated receptors (PPAR)alpha agonists, which is obtained by the combination of the classical fibrate "head group", a linker with appropriate length and a chalcone.
METHODS: Thirty seven compounds were designed and identified employing the virtual screening approach. Six compounds were then selected for synthesis and bioassay according to the virtual screening results, structural similarity, and synthetic complexity.
RESULTS: Six new compounds (4b and 4d-h) were synthesized and bioassayed. All were found to be potent PPARalpha agonists, compound 4 h being the most prominent with a 50% effective concentration value of 0.06 micromol/L.
CONCLUSION: This study provides a promising novel family of chalcones with a potential hypolipidemic effect.

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Year:  2007        PMID: 18031621     DOI: 10.1111/j.1745-7254.2007.00670.x

Source DB:  PubMed          Journal:  Acta Pharmacol Sin        ISSN: 1671-4083            Impact factor:   6.150


  1 in total

1.  Design and evaluation of chalconeimine derivatives as α-amylase inhibitors.

Authors:  Prithivirajan Balu; Jebastin Sonia Jas; Marimuthu Govindaraj
Journal:  Bioinformation       Date:  2019-07-31
  1 in total

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