Journal of Agricultural and Food Chemistry · 1999 · 160 citations · 10 references
AgricultureBiochemistryFood ScienceFood ChemistryPlant BiochemistryWine ChemistryAntioxidant DefenseFood AntioxidantsLipid OxidationLipid PeroxidationOxidation ReactionsPhenolic Compounds In WineAntioxidant MetabolitesAntioxidant Natural ProductsAntioxidantsAntioxidants In LipidsFree Radical ScavengingNatural AntioxidantsRadical Reaction MechanismsSynthetic Antioxidants
Resveratrol (3,4‘,5-trihydroxy- trans -stilbene), an antioxidant from grapes, and five other polyhydroxystilbenes were synthesized. Their antioxidative properties were evaluated in two model systems [pure lipid oxidation using the Rancimat method and 2,2-diphenyl-1-picryhydrazyl (DPPH) free radical scavenging model.] 3,3‘,4,5‘-Tetrahydroxystilbene, 3,3‘,4,5,5‘-pentahydroxystilbene, and 3,4,4‘,5-tetrahydroxystilbene were found to be more active than resveratrol in both models. A dimer of resveratrol was identified as the major radical reaction product when resveratrol was reacted with DPPH radicals. Keywords: Resveratrol derivatives; polyhydroxystilbene; antioxidant; 2,2-diphenyl-1-picryhydrazyl; free radical scavenging
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