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Synthesis of Novel Triazoles, Tetrazine, Thiadiazoles and Their Biological Activities

An expedient synthesis of novel triazoles, tetrazine and thiadiazoles, using conveniently accessible and commercially available starting materials has been achieved. The synthesized compounds were characterized by spectroscopic and elemental analyses, and screened for their antibacterial activities...

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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 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272378/
https://www.ncbi.nlm.nih.gov/pubmed/25648599
http://dx.doi.org/10.3390/molecules20022591
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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 An expedient synthesis of novel triazoles, tetrazine and thiadiazoles, using conveniently accessible and commercially available starting materials has been achieved. The synthesized compounds were characterized by spectroscopic and elemental analyses, and screened for their antibacterial activities against four different strains, namely E. coli, P. aeruginosa, S. aureus and B. megaterium. In particular, the compounds 5, 24 and 26h exhibited excellent antibacterial activities compared to the reference antibiotic. To get further insight about their behavior, these compounds were tested for their antioxidant activities via SOD-like activity, DPPH free radical scavenging activity, ABST and NO, which showed promising results. Furthermore, these compounds effectively promoted the cleavage of genomic DNA as well, in the absence of any external additives.
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spelling pubmed-62723782018-12-13 Synthesis of Novel Triazoles, Tetrazine, Thiadiazoles and Their Biological Activities Al-Omair, Mohammed A. Sayed, Abdelwahed R. Youssef, Magdy M. Molecules Article An expedient synthesis of novel triazoles, tetrazine and thiadiazoles, using conveniently accessible and commercially available starting materials has been achieved. The synthesized compounds were characterized by spectroscopic and elemental analyses, and screened for their antibacterial activities against four different strains, namely E. coli, P. aeruginosa, S. aureus and B. megaterium. In particular, the compounds 5, 24 and 26h exhibited excellent antibacterial activities compared to the reference antibiotic. To get further insight about their behavior, these compounds were tested for their antioxidant activities via SOD-like activity, DPPH free radical scavenging activity, ABST and NO, which showed promising results. Furthermore, these compounds effectively promoted the cleavage of genomic DNA as well, in the absence of any external additives. MDPI 2015-02-02 /pmc/articles/PMC6272378/ /pubmed/25648599 http://dx.doi.org/10.3390/molecules20022591 Text en © 2015 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 license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Al-Omair, Mohammed A.
Sayed, Abdelwahed R.
Youssef, Magdy M.
Synthesis of Novel Triazoles, Tetrazine, Thiadiazoles and Their Biological Activities
title Synthesis of Novel Triazoles, Tetrazine, Thiadiazoles and Their Biological Activities
title_full Synthesis of Novel Triazoles, Tetrazine, Thiadiazoles and Their Biological Activities
title_fullStr Synthesis of Novel Triazoles, Tetrazine, Thiadiazoles and Their Biological Activities
title_full_unstemmed Synthesis of Novel Triazoles, Tetrazine, Thiadiazoles and Their Biological Activities
title_short Synthesis of Novel Triazoles, Tetrazine, Thiadiazoles and Their Biological Activities
title_sort synthesis of novel triazoles, tetrazine, thiadiazoles and their biological activities
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6272378/
https://www.ncbi.nlm.nih.gov/pubmed/25648599
http://dx.doi.org/10.3390/molecules20022591
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