Bioscience Biotechnology and Biochemistry · 2003 · 78 citations · 33 references
Life SciencesBiochemistryFood ChemistryPlant BiochemistryStructure-activity RelationshipsAntioxidant DefenseFood AntioxidantsLipid PeroxidationOxidative Damage To BiomoleculesPhenolic Compound AnalysisTannin ChemistryAntioxidant MetabolitesAntioxidants In LipidsCondensed TanninsHydrolyzable TanninsPlant Extract AntioxidantsProanthocyanidin CharacterizationTannin-based Natural ProductsTea Polyphenols
Forty-three polyphenols from tea leaves were evaluated for their anti-oxidative effect against lipid peroxidation by the ferric thiocyanate method in vitro. Among these, 1,4,6-tri-O-galloyl-beta-D-glucose (hydrolyzable tannin) showed the highest anti-oxidative activity against lipid peroxidation, even stronger than that of 3-tert.-butyl-4-hydroxyanisole (BHA). The assay demonstrates that tea polyphenols, except for desgalloylated dimeric proanthocyanidins that possess a catechin structure in the upper unit and desgalloylated flavan-3-ols, and excepting theaflavin 3,3'-di-O-gallate, had more anti-oxidative activity than that of alpha-tocopherol. The chemical structure-activity relationship shows that the anti-oxidative action advanced with the condensation of two molecules of flavan-3-ols as well as with 3-O-acylation in the flavan skeleton such as that by galloyl, (3'-O-methyl)-galloyl, and p-coumaroyl groups.
33
Antioxidant properties of phenolic compounds
Catherine Rice‐Evans, Nicholas J. Miller, George Paganga · Trends in Plant Science · 1997 · 4.3K citations
Agriculture, Biochemistry, Chemistry +14
Antioxidant Effects of Some Ginger Constituents
Hiroe Kikuzaki, Nobuji Nakatani · Journal of Food Science · 1993 · 722 citations
Gen‐ichiro Nonaka, OSAMU KAWAHARA, Itsuo Nishioka · Chemical and Pharmaceutical Bulletin · 1983 · 271 citations · Full text