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Synthesis of Novel Symmetrical 1,4-Disubstituted 1,2,3-Bistriazole Derivatives via ‘Click Chemistry’ and Their Biological Evaluation

A series of symmetric bis-1,2,3-triazole compounds 2–5(a–f) were synthesized as potential antioxidant agents via click chemistry. Their structures were confirmed by (1)H-NMR and (13)C-NMR. All of the synthesized compounds were subjected to antioxidant and antimicrobial assays. The antioxidant activi...

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Autores principales: Düğdü, Esra, Ünlüer, Dilek, Çelik, Fatih, Sancak, Kemal, Alpay Karaoğlu, Şengül, Özel, Arzu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274262/
https://www.ncbi.nlm.nih.gov/pubmed/27213320
http://dx.doi.org/10.3390/molecules21050659
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author Düğdü, Esra
Ünlüer, Dilek
Çelik, Fatih
Sancak, Kemal
Alpay Karaoğlu, Şengül
Özel, Arzu
author_facet Düğdü, Esra
Ünlüer, Dilek
Çelik, Fatih
Sancak, Kemal
Alpay Karaoğlu, Şengül
Özel, Arzu
author_sort Düğdü, Esra
collection PubMed
description A series of symmetric bis-1,2,3-triazole compounds 2–5(a–f) were synthesized as potential antioxidant agents via click chemistry. Their structures were confirmed by (1)H-NMR and (13)C-NMR. All of the synthesized compounds were subjected to antioxidant and antimicrobial assays. The antioxidant activity of these compounds (AChE inhibition, DPPH and SOD activities) was evaluated. Compound 2f was found to show the highest AChE inhibition activity of all compounds, while compound 3b showed a strong inhibitory effect on DPPH radical and compound 2a was the most effective of all compounds for SOD activity. All synthesized compounds were found to possess moderate antibacterial activity against the bacteria E. coli and Y.pseudotuberculosis.
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spelling pubmed-62742622018-12-28 Synthesis of Novel Symmetrical 1,4-Disubstituted 1,2,3-Bistriazole Derivatives via ‘Click Chemistry’ and Their Biological Evaluation Düğdü, Esra Ünlüer, Dilek Çelik, Fatih Sancak, Kemal Alpay Karaoğlu, Şengül Özel, Arzu Molecules Article A series of symmetric bis-1,2,3-triazole compounds 2–5(a–f) were synthesized as potential antioxidant agents via click chemistry. Their structures were confirmed by (1)H-NMR and (13)C-NMR. All of the synthesized compounds were subjected to antioxidant and antimicrobial assays. The antioxidant activity of these compounds (AChE inhibition, DPPH and SOD activities) was evaluated. Compound 2f was found to show the highest AChE inhibition activity of all compounds, while compound 3b showed a strong inhibitory effect on DPPH radical and compound 2a was the most effective of all compounds for SOD activity. All synthesized compounds were found to possess moderate antibacterial activity against the bacteria E. coli and Y.pseudotuberculosis. MDPI 2016-05-19 /pmc/articles/PMC6274262/ /pubmed/27213320 http://dx.doi.org/10.3390/molecules21050659 Text en © 2016 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
Düğdü, Esra
Ünlüer, Dilek
Çelik, Fatih
Sancak, Kemal
Alpay Karaoğlu, Şengül
Özel, Arzu
Synthesis of Novel Symmetrical 1,4-Disubstituted 1,2,3-Bistriazole Derivatives via ‘Click Chemistry’ and Their Biological Evaluation
title Synthesis of Novel Symmetrical 1,4-Disubstituted 1,2,3-Bistriazole Derivatives via ‘Click Chemistry’ and Their Biological Evaluation
title_full Synthesis of Novel Symmetrical 1,4-Disubstituted 1,2,3-Bistriazole Derivatives via ‘Click Chemistry’ and Their Biological Evaluation
title_fullStr Synthesis of Novel Symmetrical 1,4-Disubstituted 1,2,3-Bistriazole Derivatives via ‘Click Chemistry’ and Their Biological Evaluation
title_full_unstemmed Synthesis of Novel Symmetrical 1,4-Disubstituted 1,2,3-Bistriazole Derivatives via ‘Click Chemistry’ and Their Biological Evaluation
title_short Synthesis of Novel Symmetrical 1,4-Disubstituted 1,2,3-Bistriazole Derivatives via ‘Click Chemistry’ and Their Biological Evaluation
title_sort synthesis of novel symmetrical 1,4-disubstituted 1,2,3-bistriazole derivatives via ‘click chemistry’ and their biological evaluation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6274262/
https://www.ncbi.nlm.nih.gov/pubmed/27213320
http://dx.doi.org/10.3390/molecules21050659
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