Literature DB >> 23818394

Synthesis and radical scavenging activities of resveratrol analogs.

René Csuk1, Sabrina Albert, Bianka Siewert.   

Abstract

Highly substituted polyhydroxylated (E)-stilbenes were synthesized by Mizoroki-Heck reactions and tested for their ability to act as radical scavenger. One of the 56 stilbenes included in this study and investigated in DPPH assays gave an SC50 value of 11.0 μM, hence exhibiting an about 9.3 times higher activity than resveratrol. As shown in a photometric SRB assay using mouse NiH 3T3 fibroblasts, this compound is not cytotoxic up to concentrations of <30 μM.
© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  French paradox; Radical scavengers; Resveratrol analogs

Mesh:

Substances:

Year:  2013        PMID: 23818394     DOI: 10.1002/ardp.201300081

Source DB:  PubMed          Journal:  Arch Pharm (Weinheim)        ISSN: 0365-6233            Impact factor:   3.751


  2 in total

1.  The resveratrol derivatives trans-3,5-dimethoxy-4-fluoro-4'-hydroxystilbene and trans-2,4',5-trihydroxystilbene decrease oxidative stress and prolong lifespan in Caenorhabditis elegans.

Authors:  Nadine Fischer; Christian Büchter; Karoline Koch; Sabrina Albert; René Csuk; Wim Wätjen
Journal:  J Pharm Pharmacol       Date:  2016-11-23       Impact factor: 3.765

2.  The Synthesis and Accumulation of Resveratrol Are Associated with Veraison and Abscisic Acid Concentration in Beihong (Vitis vinifera × Vitis amurensis) Berry Skin.

Authors:  Junfang Wang; Shuqin Wang; Guotian Liu; Everard J Edwards; Wei Duan; Shaohua Li; Lijun Wang
Journal:  Front Plant Sci       Date:  2016-11-03       Impact factor: 5.753

  2 in total

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