Synthesis and membrane protective activity of bis-sulfides derived from monoterpenoids and monosaccharides
- Authors: Pestova S.V.1, Izmest’ev E.S.1, Shevchenko O.G.2, Rubtsova S.A.1, Kuchin A.V.1
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Affiliations:
- Institute of Chemistry, Komi Science Centre, Ural Division
- Institute of Biology, Komi Science Centre, Ural Division
- Issue: Vol 43, No 3 (2017)
- Pages: 302-310
- Section: Article
- URL: https://journals.rcsi.science/1068-1620/article/view/228528
- DOI: https://doi.org/10.1134/S1068162017030141
- ID: 228528
Cite item
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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