Resveratrol and resveratrol analogues--structure-activity relationship

Pharm Res. 2010 Jun;27(6):1042-8. doi: 10.1007/s11095-010-0090-1. Epub 2010 Mar 16.

Abstract

Resveratrol (3,4',5-trihydroxy-trans-stilbene) is a compound found in wine and is held responsible for a number of beneficial effects of red wine. Besides the prevention of heart disease and significant anti-inflammatory effects, resveratrol might inhibit tumor cell growth and even play a role in the aging process. We here describe the structure-activity relationship of resveratrol and analogues of resveratrol regarding the free radical scavenging and antitumor effects of this exciting natural compound. In addition, we have synthesized a number of analogues of resveratrol with the aim to further improve the beneficial effects of resveratrol. Our studies were based on the analysis of structural properties, which were responsible for the most important effects of this compound. Striking in vivo effects can be observed with hexahydroxystilbene (M8), the most effective synthetic analogue of resveratrol. We could show that M8 inhibits tumor as well as metastasis growth of human melanoma in two different animal models, alone and in combination with dacarbacine.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / pharmacology*
  • Free Radical Scavengers / chemistry*
  • Free Radical Scavengers / metabolism
  • Free Radical Scavengers / pharmacology*
  • Humans
  • Neoplasms / drug therapy*
  • Resveratrol
  • Stilbenes / chemistry*
  • Stilbenes / metabolism
  • Stilbenes / pharmacology*
  • Structure-Activity Relationship

Substances

  • Antineoplastic Agents
  • Free Radical Scavengers
  • Stilbenes
  • Resveratrol