Free Radical Research · 1997 · 131 citations · 15 references
Life SciencesBiochemistryFood ScienceFood ChemistryStructure-activity RelationshipsVegetable ScienceAntioxidant DefenseBioactive Food ComponentsFood AntioxidantsLipid OxidationLipid PeroxidationOxidative Damage To BiomoleculesAntioxidant Activity AssaysAntioxidant InhibitionAntioxidant PropertiesFlavonoid GlycosidesHydroxycinnamic AcidsNatural AntioxidantsPhenolic CompoundsPlant Phenolics
We have examined the antioxidant activity of the major phenolic compounds in Broccoli: two flavonol glycosides (quercetin 3-O-sophoroside and kaempferol 3-O-sophoroside) and four hydroxycinnamic acid esters (1,2'-disinapoyl-2-feruloyl gentiobiose, 1-sinapoyl-2-feruloyl gentiobiose, 1,2,2'-trisinapoyl gentiobiose and 1,2-disinapoyl gentiobiose). The Trolox C equivalent antioxidant capacity (TEAC) and inhibition of iron/ascorbate-induced lipid peroxidation of phosphatidyl choline vesicles were measured. In the aqueous phase TEAC assay, the two flavonol glycosides were less active than their respective aglycones. TEAC values for the hydroxycinnamic acid esters were less than the sum of their constituent hydroxycinnamic acids on a molar basis. Quercetin 3-O-sophoroside was a potent inhibitor of lipid peroxidation, in contrast to kaempferol 3-O-sophoroside. The hydroxycinnamic acid esters were highly effective at preventing lipid damage with the exception of 1,2,2'-trisinapoyl gentiobiose. The six compounds analysed herein demonstrate the antioxidant activity of the major phenolics in broccoli and indicate the effect on antioxidant activity of sugar substitutions in the phenolic B ring.
15
The Relative Antioxidant Activities of Plant-Derived Polyphenolic Flavonoids
Catherine Rice‐Evans, Nicholas J. Miller, Paul Bolwell et al. · Free Radical Research · 1995 · 2.2K citations
Agriculture, Botany, Plant Sciences +15
Flavonoid intake and coronary mortality in Finland: a cohort study
Paul Knekt, Antti Reunanen, J. Maatela · BMJ · 1996 · 1.3K citations