Abstract
The method of competing reactions was used to determine the rate constants of the reaction of resveratrol (RVT) with peroxyl radicals formed on decomposition of the azoinitiator ААРН in aqueous solutions at 37 °С. The polymethine dye A (3,3′-di-γ-sulfopropyl-9-metylthiacarbocyanine-betaine pyridinium salt) was used as a competing acceptor of radicals. It was found that resveratrol can be involved in the reaction with natural thiols, glutathione (GSH) and cysteine (CSH), in aqueous solutions at 37 °С. The reaction of RVT with thiols (thiol—еne reaction) follows a chain mechanism and accelerates in the presence of Н2О2. The results obtained can be useful for understanding the physiological role of thiols in oxidation processes.
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Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 11, pp. 2145—2151, November, 2017.
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Zinatullina, K.M., Khrameeva, N.P., Kasaikina, O.T. et al. Kinetic characteristics of the reaction of resveratrol with peroxyl radicals and natural thiols in aqueous medium. Russ Chem Bull 66, 2145–2151 (2017). https://doi.org/10.1007/s11172-017-1995-1
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DOI: https://doi.org/10.1007/s11172-017-1995-1