Posted by Chantel Martiromo. research contributed by PubMed
According to the study by the Renmin University of China, posted in PubMed, the isoflavonoid genistein was found to be a better antioxidant than the
isomeric flavonoid apigenin in phosphatidyl liposomes at pH 7.4. The
higher antioxidation activity of genistein compared with apigenin is in
agreement with its lower oxidation potential (0.73 vs 0.86 V as
determined by cyclic voltammetry in aqueous solution of pH= 7.4), lower
dissociation enthalpy (87.03 vs 87.88 kcal mol(-1) as calculated for the
more reducing 4'-hydroxyl group), and higher radical scavenging
capacity in the TEAC assay. On the basis of quantum mechanical
calculations for genistein and apigenin in comparison with the flavonoid
naringenin and the isoflavonoids puerarin, daidzein,
and equol, a lower dipole moment and a larger deviation for the A-to-B
dihedral angle from coplanarity (39.3 degrees for genistein, 18.5
degrees for apigenin) are suggested to be important for the increased
antioxidant efficiency at water/lipid interfaces among (iso) flavonoids
with an equal number of phenolic groups.
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