Synthesis of 3,5-Di-tert-butyl-1,2-dihydroxybenzene Derivatives and Their Effect on Free-Radical Oxidation of Hexane and Oxygen Activation Ability of Neutrophils


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Abstract

C6-Substituted derivatives of 3,5-di-tert-butyl-1,2-dihydroxybenzene have been synthesized, and their effect on radiation-induced free-radical oxidation of n-hexane and production of reactive oxygen and chlorine forms in neutrophils have been studied. It has been shown the introduction of the phenylhydrazone and phenylazomethine groups significantly increases the antioxidant activity of pyrocatechol derivatives. For six compounds, the ability to prevent the development of oxidative stress due to hyperproduction of active oxygen intermediates and HOCl/OCl in neutrophils has been revealed.

About the authors

G. A. Ksendzova

Research Institute of Physical and Chemical Problems

Email: ksja-bn@tut.by
Belarus, ul. Leningradskaya 14, Minsk, 220050

N. I. Ostrovskaya

Research Institute of Physical and Chemical Problems

Email: ksja-bn@tut.by
Belarus, ul. Leningradskaya 14, Minsk, 220050

G. N. Semenkova

Belarusian State University

Author for correspondence.
Email: ksja-bn@tut.by
Belarus, Minsk

V. L. Sorokin

Belarusian State University

Email: ksja-bn@tut.by
Belarus, Minsk

P. A. Shishkanova

Belarusian State University

Email: ksja-bn@tut.by
Belarus, Minsk

O. I. Shadyro

Research Institute of Physical and Chemical Problems; Belarusian State University

Email: ksja-bn@tut.by
Belarus, ul. Leningradskaya 14, Minsk, 220050; Minsk


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