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Chemistry of Substituted Thiazinanes and Their Derivatives
Thiazinanes and its isomeric forms represent one of the most important heterocyclic compounds, and their derivatives represented a highly potent drug in disease treatment such as, 1,1-dioxido-1,2-thiazinan-1,6-naphthyridine, which has been shown to have anti-HIV activity by a mechanism that should w...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730229/ https://www.ncbi.nlm.nih.gov/pubmed/33260625 http://dx.doi.org/10.3390/molecules25235610 |
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author | Hassan, Alaa A. Bräse, Stefan Aly, Ashraf A. Tawfeek, Hendawy N. |
author_facet | Hassan, Alaa A. Bräse, Stefan Aly, Ashraf A. Tawfeek, Hendawy N. |
author_sort | Hassan, Alaa A. |
collection | PubMed |
description | Thiazinanes and its isomeric forms represent one of the most important heterocyclic compounds, and their derivatives represented a highly potent drug in disease treatment such as, 1,1-dioxido-1,2-thiazinan-1,6-naphthyridine, which has been shown to have anti-HIV activity by a mechanism that should work as anti-AIDS treatment, while (Z)-methyl 3-(naphthalen-1-ylimino)- 2-thia-4-azaspiro[5 5]undecane-4-carbodithioate showed analgesic activity, cephradine was used as antibiotic and chlormezanone was utilized as anticoagulants. All publications were interested in the chemistry of thiazine (partially or fully unsaturated heterocyclic six-membered ring containing nitrogen and sulfur), but no one was dealing with thiazinane itself which encouraged us to shed new light on these interesting heterocycles. This review was focused on the synthetic approaches of thiazinane derivatives and their chemical reactivity. |
format | Online Article Text |
id | pubmed-7730229 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77302292020-12-12 Chemistry of Substituted Thiazinanes and Their Derivatives Hassan, Alaa A. Bräse, Stefan Aly, Ashraf A. Tawfeek, Hendawy N. Molecules Review Thiazinanes and its isomeric forms represent one of the most important heterocyclic compounds, and their derivatives represented a highly potent drug in disease treatment such as, 1,1-dioxido-1,2-thiazinan-1,6-naphthyridine, which has been shown to have anti-HIV activity by a mechanism that should work as anti-AIDS treatment, while (Z)-methyl 3-(naphthalen-1-ylimino)- 2-thia-4-azaspiro[5 5]undecane-4-carbodithioate showed analgesic activity, cephradine was used as antibiotic and chlormezanone was utilized as anticoagulants. All publications were interested in the chemistry of thiazine (partially or fully unsaturated heterocyclic six-membered ring containing nitrogen and sulfur), but no one was dealing with thiazinane itself which encouraged us to shed new light on these interesting heterocycles. This review was focused on the synthetic approaches of thiazinane derivatives and their chemical reactivity. MDPI 2020-11-28 /pmc/articles/PMC7730229/ /pubmed/33260625 http://dx.doi.org/10.3390/molecules25235610 Text en © 2020 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Hassan, Alaa A. Bräse, Stefan Aly, Ashraf A. Tawfeek, Hendawy N. Chemistry of Substituted Thiazinanes and Their Derivatives |
title | Chemistry of Substituted Thiazinanes and Their Derivatives |
title_full | Chemistry of Substituted Thiazinanes and Their Derivatives |
title_fullStr | Chemistry of Substituted Thiazinanes and Their Derivatives |
title_full_unstemmed | Chemistry of Substituted Thiazinanes and Their Derivatives |
title_short | Chemistry of Substituted Thiazinanes and Their Derivatives |
title_sort | chemistry of substituted thiazinanes and their derivatives |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7730229/ https://www.ncbi.nlm.nih.gov/pubmed/33260625 http://dx.doi.org/10.3390/molecules25235610 |
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