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Synthesis and Biological Evaluation of Bisthiazoles and Polythiazoles

Small heterocyclic compounds containing nitrogen and sulfur atoms, such as thiazole derivatives, represent a significant class of organic azoles that exhibit promising bioactivities and have a great potential in medicinal and agricultural fields. A convenient and high-yielding synthetic approach for...

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Detalles Bibliográficos
Autores principales: Al-Omair, Mohammed A., Sayed, Abdelwahed R., Youssef, Magdy M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099618/
https://www.ncbi.nlm.nih.gov/pubmed/29747479
http://dx.doi.org/10.3390/molecules23051133
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author Al-Omair, Mohammed A.
Sayed, Abdelwahed R.
Youssef, Magdy M.
author_facet Al-Omair, Mohammed A.
Sayed, Abdelwahed R.
Youssef, Magdy M.
author_sort Al-Omair, Mohammed A.
collection PubMed
description Small heterocyclic compounds containing nitrogen and sulfur atoms, such as thiazole derivatives, represent a significant class of organic azoles that exhibit promising bioactivities and have a great potential in medicinal and agricultural fields. A convenient and high-yielding synthetic approach for a range of organic molecules is presented. The nuclease-like activities of compounds were studied with the aid of E. coli AB1157 DNA and agarose gel electrophoresis. The antioxidant evaluation of the compounds was carried out with different antioxidant techniques, such as ABTS and NO scavenging efficiency. The antibacterial behavior was evaluated against various bacterial strains, both Gram-positive and -negative, and the minimum inhibitory concentration (MIC) values of these compounds were determined. The antiproliferative activities and IC(50) values of the synthesized organic molecules compounds against HEPG-2, MCF-7, and HCT-116 cell lines were evaluated.
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spelling pubmed-60996182018-11-13 Synthesis and Biological Evaluation of Bisthiazoles and Polythiazoles Al-Omair, Mohammed A. Sayed, Abdelwahed R. Youssef, Magdy M. Molecules Article Small heterocyclic compounds containing nitrogen and sulfur atoms, such as thiazole derivatives, represent a significant class of organic azoles that exhibit promising bioactivities and have a great potential in medicinal and agricultural fields. A convenient and high-yielding synthetic approach for a range of organic molecules is presented. The nuclease-like activities of compounds were studied with the aid of E. coli AB1157 DNA and agarose gel electrophoresis. The antioxidant evaluation of the compounds was carried out with different antioxidant techniques, such as ABTS and NO scavenging efficiency. The antibacterial behavior was evaluated against various bacterial strains, both Gram-positive and -negative, and the minimum inhibitory concentration (MIC) values of these compounds were determined. The antiproliferative activities and IC(50) values of the synthesized organic molecules compounds against HEPG-2, MCF-7, and HCT-116 cell lines were evaluated. MDPI 2018-05-10 /pmc/articles/PMC6099618/ /pubmed/29747479 http://dx.doi.org/10.3390/molecules23051133 Text en © 2018 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 Article
Al-Omair, Mohammed A.
Sayed, Abdelwahed R.
Youssef, Magdy M.
Synthesis and Biological Evaluation of Bisthiazoles and Polythiazoles
title Synthesis and Biological Evaluation of Bisthiazoles and Polythiazoles
title_full Synthesis and Biological Evaluation of Bisthiazoles and Polythiazoles
title_fullStr Synthesis and Biological Evaluation of Bisthiazoles and Polythiazoles
title_full_unstemmed Synthesis and Biological Evaluation of Bisthiazoles and Polythiazoles
title_short Synthesis and Biological Evaluation of Bisthiazoles and Polythiazoles
title_sort synthesis and biological evaluation of bisthiazoles and polythiazoles
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6099618/
https://www.ncbi.nlm.nih.gov/pubmed/29747479
http://dx.doi.org/10.3390/molecules23051133
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