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Synthesis and Biological Activity of Unsymmetrical Monoterpenylhetaryl Disulfides

New unsymmetrical monoterpenylhetaryl disulfides based on heterocyclic disulfides and monoterpene thiols were synthesized for the first time in 48–88% yields. Hydrolysis of disulfides with fragments of methyl esters of 2-mercaptonicotinic acid was carried out in 73–95% yields. The obtained compounds...

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Autores principales: Sudarikov, Denis V., Gyrdymova, Yulia V., Borisov, Alexander V., Lukiyanova, Julia M., Rumyantcev, Roman V., Shevchenko, Oksana G., Baidamshina, Diana R., Zakarova, Nargiza D., Kayumov, Airat R., Sinegubova, Ekaterina O., Volobueva, Alexandrina S., Zarubaev, Vladimir V., Rubtsova, Svetlana A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416111/
https://www.ncbi.nlm.nih.gov/pubmed/36014334
http://dx.doi.org/10.3390/molecules27165101
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author Sudarikov, Denis V.
Gyrdymova, Yulia V.
Borisov, Alexander V.
Lukiyanova, Julia M.
Rumyantcev, Roman V.
Shevchenko, Oksana G.
Baidamshina, Diana R.
Zakarova, Nargiza D.
Kayumov, Airat R.
Sinegubova, Ekaterina O.
Volobueva, Alexandrina S.
Zarubaev, Vladimir V.
Rubtsova, Svetlana A.
author_facet Sudarikov, Denis V.
Gyrdymova, Yulia V.
Borisov, Alexander V.
Lukiyanova, Julia M.
Rumyantcev, Roman V.
Shevchenko, Oksana G.
Baidamshina, Diana R.
Zakarova, Nargiza D.
Kayumov, Airat R.
Sinegubova, Ekaterina O.
Volobueva, Alexandrina S.
Zarubaev, Vladimir V.
Rubtsova, Svetlana A.
author_sort Sudarikov, Denis V.
collection PubMed
description New unsymmetrical monoterpenylhetaryl disulfides based on heterocyclic disulfides and monoterpene thiols were synthesized for the first time in 48–88% yields. Hydrolysis of disulfides with fragments of methyl esters of 2-mercaptonicotinic acid was carried out in 73–95% yields. The obtained compounds were evaluated for antioxidant, antibacterial, antifungal activity, cytotoxicity and mutagenicity.
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spelling pubmed-94161112022-08-27 Synthesis and Biological Activity of Unsymmetrical Monoterpenylhetaryl Disulfides Sudarikov, Denis V. Gyrdymova, Yulia V. Borisov, Alexander V. Lukiyanova, Julia M. Rumyantcev, Roman V. Shevchenko, Oksana G. Baidamshina, Diana R. Zakarova, Nargiza D. Kayumov, Airat R. Sinegubova, Ekaterina O. Volobueva, Alexandrina S. Zarubaev, Vladimir V. Rubtsova, Svetlana A. Molecules Article New unsymmetrical monoterpenylhetaryl disulfides based on heterocyclic disulfides and monoterpene thiols were synthesized for the first time in 48–88% yields. Hydrolysis of disulfides with fragments of methyl esters of 2-mercaptonicotinic acid was carried out in 73–95% yields. The obtained compounds were evaluated for antioxidant, antibacterial, antifungal activity, cytotoxicity and mutagenicity. MDPI 2022-08-10 /pmc/articles/PMC9416111/ /pubmed/36014334 http://dx.doi.org/10.3390/molecules27165101 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sudarikov, Denis V.
Gyrdymova, Yulia V.
Borisov, Alexander V.
Lukiyanova, Julia M.
Rumyantcev, Roman V.
Shevchenko, Oksana G.
Baidamshina, Diana R.
Zakarova, Nargiza D.
Kayumov, Airat R.
Sinegubova, Ekaterina O.
Volobueva, Alexandrina S.
Zarubaev, Vladimir V.
Rubtsova, Svetlana A.
Synthesis and Biological Activity of Unsymmetrical Monoterpenylhetaryl Disulfides
title Synthesis and Biological Activity of Unsymmetrical Monoterpenylhetaryl Disulfides
title_full Synthesis and Biological Activity of Unsymmetrical Monoterpenylhetaryl Disulfides
title_fullStr Synthesis and Biological Activity of Unsymmetrical Monoterpenylhetaryl Disulfides
title_full_unstemmed Synthesis and Biological Activity of Unsymmetrical Monoterpenylhetaryl Disulfides
title_short Synthesis and Biological Activity of Unsymmetrical Monoterpenylhetaryl Disulfides
title_sort synthesis and biological activity of unsymmetrical monoterpenylhetaryl disulfides
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9416111/
https://www.ncbi.nlm.nih.gov/pubmed/36014334
http://dx.doi.org/10.3390/molecules27165101
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