Synthesis and membrane protective activity of bis-sulfides derived from monoterpenoids and monosaccharides


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Abstract

Hydroxyl- and chloroethyl derivatives of neomenthane- and isobornanethiol in yields of to 80% were synthesized. They served as the basis for the preparation of new bis-sulfides with diacetone-protected galacto- and fructopyranose fragments in yields up to 98%. The bis-sulfides synthesized were screened for membrane protective and antioxidant properties in a model cell system (in vitro) based on their ability to inhibit the H2O2-induced hemolysis of erythrocytes and retard the oxyhemoglobin oxidation.

About the authors

S. V. Pestova

Institute of Chemistry, Komi Science Centre, Ural Division

Author for correspondence.
Email: pestova-sv@chemi.komisc.ru
Russian Federation, Syktyvkar, 167987

E. S. Izmest’ev

Institute of Chemistry, Komi Science Centre, Ural Division

Email: pestova-sv@chemi.komisc.ru
Russian Federation, Syktyvkar, 167987

O. G. Shevchenko

Institute of Biology, Komi Science Centre, Ural Division

Email: pestova-sv@chemi.komisc.ru
Russian Federation, Syktyvkar, 167000

S. A. Rubtsova

Institute of Chemistry, Komi Science Centre, Ural Division

Email: pestova-sv@chemi.komisc.ru
Russian Federation, Syktyvkar, 167987

A. V. Kuchin

Institute of Chemistry, Komi Science Centre, Ural Division

Email: pestova-sv@chemi.komisc.ru
Russian Federation, Syktyvkar, 167987

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