4.5 Article

Resveratrol and Resveratrol Analogues-Structure-Activity Relationship

Journal

PHARMACEUTICAL RESEARCH
Volume 27, Issue 6, Pages 1042-1048

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s11095-010-0090-1

Keywords

apoptosis; gallic acid; resveratrol; ribonucleotide reductase; stilbene analogues

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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.

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