1. Academic Validation
  2. Resveratrol derivatives as promising chemopreventive agents with improved potency and selectivity

Resveratrol derivatives as promising chemopreventive agents with improved potency and selectivity

  • Mol Nutr Food Res. 2011 Aug;55(8):1249-65. doi: 10.1002/mnfr.201100122.
Tamara P Kondratyuk 1 Eun-Jung Park Laura E Marler Soyoun Ahn Yang Yuan Yongsoo Choi Rui Yu Richard B van Breemen Bin Sun Juma Hoshino Mark Cushman Katherine C Jermihov Andrew D Mesecar Clinton J Grubbs John M Pezzuto
Affiliations

Affiliation

  • 1 College of Pharmacy, University of Hawaii at Hilo, Hilo, HI 96720, USA.
Abstract

Scope: Despite scores of investigations, the actual impact of resveratrol (3,5,4'-trihydroxy-trans-stilbene) on human health, as a dietary component or supplement, remains moot. This is due to many factors, such as relatively low potency, pleiotropic mechanisms, and rapid metabolism. Nonetheless, as a promiscuous molecule that interacts with numerous targets, resveratrol can be viewed as a scaffold for designing structural relatives potentially capable of mediating more intense responses with greater mechanistic stringency.

Methods and results: We currently report the synthesis and biological evaluation of 92 stilbene analogs. The compounds were tested with in vitro assays for activation of quinone reductase 1, inhibition of quinone reductase 2, nitric oxide production, aromatase, NFκB, 12-O-tetradecanoylphorbol-13-acetate (TPA)-induced ornithine decarboxylase, or cyclooxygenase-1 and -2, quenching of 2,2-diphenyl-1-picrylhydrazyl free radical, interaction with estrogen receptors, and as antiproliferative agents. Several compounds were found to mediate responses with much greater potency than resveratrol; some mediated pleiotropic responses, as is the case with the parent molecule, but Others were highly specific or totally inactive. When administered to rats, higher serum concentrations and greater stability was demonstrated with prototype lead molecules.

Conclusion: Owing to structural simplicity, facile syntheses are available for large-scale production. These data support the promise of more advanced development of novel resveratrol derivatives as drug entities.

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  • HY-112554