Quantum-chemical Study on the Thermodynamical Aspect of Competitive Inhibition of Ribonucleotide Reductase by trans-Resveratrol, trans- Piceatannol and Hydroxyurea

Title:Quantum-chemical Study on the Thermodynamical Aspect of Competitive Inhibition of Ribonucleotide Reductase by trans-Resveratrol, trans- Piceatannol and Hydroxyurea

Volume: 12 Issue: 2

Author(s): Krzysztof Eder, Damian Mikulski and Marcin Molski

Affiliation:

Keywords: Enzyme inhibition, ribonucleotide reductase, trans-resveratrol, trans-piceatannol.

Abstract: Ribonucleotide reductase is an enzyme that catalyzes the formation of deoxyribonucleotides from ribonucleotides. We present for the first time a quantum-chemical study of the thermodynamics of reactions of naturally occurring potent inhibitors (trans-resveratrol, trans-piceatannol and hydroxyurea) of ribonucleotide reductase with tyrosine radical and cysteine radical, scavenging of which is crucial for the inhibition of the enzyme. Density functional theory has been applied to compute the Gibbs free enthalpy changes for these reactions in the gas phase and in the presence of water medium. Various reaction pathways have been analyzed. The results obtained prove that trans-resveratrol 4’-OH group is mainly responsible for effective reaction with these enzymatic free radicals. In water medium, the reactions studied are characterized by more negative values of the Gibbs free enthalpy changes than in vacuum. It was found that transresveratrol and trans-piceatannol may be efficient inhibitors of the enzyme (trans-piceatannol is more efficient than transresveratrol). Because inhibition of ribonucleotide reductase is essential for blockage of the cancer development pathways, the polyphenols studied may block diverse processes (including cancerogenesis) by inhibition of free radical reaction steps that occur during the catalytic action of this enzyme.

Cite this article as:

Eder Krzysztof, Mikulski Damian and Molski Marcin, Quantum-chemical Study on the Thermodynamical Aspect of Competitive Inhibition of Ribonucleotide Reductase by trans-Resveratrol, trans- Piceatannol and Hydroxyurea, Letters in Drug Design & Discovery 2015; 12 (2) . https://dx.doi.org/10.2174/1570180811666140909005756