Quantum-chemical study on relationship between structure and antioxidant properties of hepatoprotective compounds occurring in Cynara scolymus and Silybum marianum

Abstract

Accurate quantum computations based on the density functional theory have been performed to study the relationship between the electronic geometry and antioxidant capacity of chlorogenic acid, silybin and all geometric stereoisomers of cynarine, isolated from plant extract of Cynara scolymus and Silybum marianum. To elucidate their antioxidant activity, the HOMO orbital distribution, adiabatic ionization potential (AIP), spin density in free radicals, homolytic dissociation enthalpies (BDE), and proton dissociation enthalpies (PDE) of the O – H bonds have been calculated. For minimum energy conformations, the antioxidative parameters were quantitatively analyzed at the B3LYP/6-311G(d,p) level of theory. The results have shown that the hydrogen transfer mechanism is more preferable in nonpolar medium than in water. From the results obtained we can conclude that SET-PT (single electron transfer followed by proton transfer) is the most preferred mechanism in water medium. The catechol moiety and planar geometry of trans-stilbene and cis-stilbene moieties in cynarine stereoisomers, chlorogenic acid and their phenoxy radicals strongly contribute to enhancement of the antioxidant activity of these compounds. Trans,trans-cynarine appears to be the best candidate for proton and hydrogen atom donor. It has been predicted that cis,cis, trans,cis and cis,trans stereoisomers of cynarine show antioxidant capacity. Our study shows that all of the investigated compounds reveal strong antioxidant activity.