engleski

FREE RADICAL SCAVENGING POTENCY OF EQUOL

Kinetic analysis performed by using Transitivity Code indicates that phenolic hydrogens of physiologically active equol molecule are much more abstractable than C-ring hydrogens. Obtained results are opposite to very recently published statements that aliphatic C−H bonds of natural compounds may play significant role in antioxidant action. Unequivocally, phenolic O−H bonds are responsible for antiradical activity of equol. The contribution of equol’s C-ring hydrogens to free radical scavenging is negligible.

equol ; C-H bonds ; C-O bonds ; kinetic analysis

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