Abstract
Neomenthane and isobornane thiol-derived sulfanyl imines were prepared in yields of up to 85%. On the basis of the capacity of the sulfanyl imines obtained to inhibit the H2H2- and AAPH-induced erythrocyte hemolysis and impede the accumulation of secondary products of lipid peroxidation and hemoglobin oxidation, they were shown to display membrane protective and antioxidant properties.
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Abbreviations
- AO:
-
antioxidants
- NCS:
-
N-chlorosuccinimide
- LPO:
-
lipid peroxidation
- AAPH:
-
2,2-azobis(amidinopropane) dihydrochloride
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Original Russian Text © E.S. Izmest’ev, D.V. Sudarikov, O.G. Shevchenko, S.A. Rubtsova, A.V. Kutchin, 2015, published in Bioorganicheskaya Khimiya, 2015, Vol. 41, No. 1, pp. 90–96.
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Izmest’ev, E.S., Sudarikov, D.V., Shevchenko, O.G. et al. The synthesis and membrane protective properties of sulfanyl imines derived from neomenthane and isobornane thiols. Russ J Bioorg Chem 41, 77–82 (2015). https://doi.org/10.1134/S1068162014050070
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DOI: https://doi.org/10.1134/S1068162014050070