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Redox Report
Communications in Free Radical Research
Volume 16, 2011 - Issue 6
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Research article

Exploration of pro-oxidant and antioxidant activities of the flavonoid myricetin

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Pages 242-247 | Published online: 19 Jul 2013

Figures & data

Figure 1. Structure of myricetin.

Figure 1. Structure of myricetin.

Figure 2. Effects of myricetin on TBARS formation in various systems and variants of the deoxyribose degradation assay; 100% TBARS represents mean formation in the FeCl3 or FeEDTA variant of the classical ascorbic acid–H2O2 system; bars are mean ± SD; N = 3, letters indicate different levels of significance between effects (95% Duncan's multiple range test).

Figure 2. Effects of myricetin on TBARS formation in various systems and variants of the deoxyribose degradation assay; 100% TBARS represents mean formation in the FeCl3 or FeEDTA variant of the classical ascorbic acid–H2O2 system; bars are mean ± SD; N = 3, letters indicate different levels of significance between effects (95% Duncan's multiple range test).

Figure 3. Dose–response curves of TBARS formation depending on the myricetin:Fe ratio in various systems and variants of the deoxyribose degradation assay; 100% TBARS represents mean formation in the FeCl3 or FeEDTA variant of the classical ascorbic acid–H2O2 system; X-axis has logarithmic scaling but values are not transformed.

Figure 3. Dose–response curves of TBARS formation depending on the myricetin:Fe ratio in various systems and variants of the deoxyribose degradation assay; 100% TBARS represents mean formation in the FeCl3 or FeEDTA variant of the classical ascorbic acid–H2O2 system; X-axis has logarithmic scaling but values are not transformed.

Figure 4. Redox reactions of myricetin.

Figure 4. Redox reactions of myricetin.

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