1998
DOI: 10.1016/s0006-2952(98)00128-2
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Study on the Inhibitory Effect of Tannins and Flavonoids against the 1,1-Diphenyl-2-picrylhydrazyl Radical

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Cited by 551 publications
(394 citation statements)
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“…[4][5][6][7][8][9][10] The antioxidant activity of phenolic compounds is inuenced by the number and position of phenolic hydroxyls and other substituents, and glycosylation of the molecules. 11,12 Furthermore, antitumor properties have also been attributed to different phenolic compounds, including avones. 13 Other important antioxidant molecules are tocopherols, which are considered as one of the most important antioxidants to combat oxidative stress, because they inhibit the production of peroxyl radicals, protecting cells of oxidative damage to low density lipoproteins, proteins and DNA, and of membrane degeneration due to peroxidation of polyunsaturated fatty acids.…”
Section: Introductionmentioning
confidence: 99%
“…[4][5][6][7][8][9][10] The antioxidant activity of phenolic compounds is inuenced by the number and position of phenolic hydroxyls and other substituents, and glycosylation of the molecules. 11,12 Furthermore, antitumor properties have also been attributed to different phenolic compounds, including avones. 13 Other important antioxidant molecules are tocopherols, which are considered as one of the most important antioxidants to combat oxidative stress, because they inhibit the production of peroxyl radicals, protecting cells of oxidative damage to low density lipoproteins, proteins and DNA, and of membrane degeneration due to peroxidation of polyunsaturated fatty acids.…”
Section: Introductionmentioning
confidence: 99%
“…This procedure is fast and, at the same time, sensitive (Yokozawa et al, 1998). Hydrogen donor molecules present in the extract that react with the DPPH radical cause a decrease in the intensity of absorption at 517 nm and can help identify extracts with anti-radical compounds.…”
Section: Resultsmentioning
confidence: 99%
“…DPPH (1,1-diphenyl-2-picrylhydrazyl) solution were prepared in methanol, as previously published (Yokozawa et al, 1998;Pellat et al, 2004). In a 96-well microplate, 10 μL of a 1 mM solution of DPPH and appropriate volumes of antioxidant (to obtain final concentrations of 0.1, 0.5, 1.0, 1.5 and 2.0 mg/mL) were added and the final volume of 100 μL completed with methanol.…”
Section: Antioxidant Activitymentioning
confidence: 99%
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“…These compounds had a high DPPH scavenging activity, such as quercetin (IC 50 = 0.83 µg/mL) and kaempferol (IC 50 = 1.87 µg/mL) (Cho et al, 2003). Almost all tannin compounds had been studied to show high DPPH scavenging activity in a small concentration range [24]. The compound content caused the matoa leaves and stem bark extracts to have very strong DPPH scavenging activity, but both extracts did not have good tyrosinase inhibitory ability.…”
Section: Antioxidant Activity Test Of the Matoa Stem Bark Extract Framentioning
confidence: 99%