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• W2263940211 abstract "Resveratrol (3,5,4′-trihydroxystilbene) is a phytoalexin produced by plants. Resveratrol is known for its anti-cancer, antiviral and antioxidant properties. We prepared imine analogs of resveratrol ((hydroxyphenyliminomethyl)phenols) and tested their antioxidant activity. All prepared resveratrol analogs were able to scavenge 2,2-diphenyl-1-picrylhydrazyl (DPPH), galvinoxyl radical (GOR) and 2,2′-azino-bis(3-ethylbenzothiazoline)-6-sulphonic acid (ABTS) radicals. The antioxidant activity efficiency correlated with the number and position of hydroxyl groups. The most effective antioxidants were resveratrol analogs containing three hydroxyl groups in the benzylidene part of their molecules. These results provide new insights into the relationship between the chemical structure and biological activity of resveratrol analogs." @default.
• W2263940211 created "2016-06-24" @default.
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• W2263940211 date "2016-01-21" @default.
• W2263940211 modified "2023-10-15" @default.
• W2263940211 title "The Scavenging of DPPH, Galvinoxyl and ABTS Radicals by Imine Analogs of Resveratrol" @default.
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• W2263940211 doi "https://doi.org/10.3390/molecules21010127" @default.
• W2263940211 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/4759939" @default.
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