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Benzimidazole-Triazole Hybrids as Antimicrobial and Antiviral Agents: A Systematic Review

Bacterial infections have attracted the attention of researchers in recent decades, especially due to the special problems they have faced, such as their increasing diversity and resistance to antibiotic treatment. The emergence and development of the SARS-CoV-2 infection stimulated even more resear...

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Autor principal: Marinescu, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376251/
https://www.ncbi.nlm.nih.gov/pubmed/37508316
http://dx.doi.org/10.3390/antibiotics12071220
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author Marinescu, Maria
author_facet Marinescu, Maria
author_sort Marinescu, Maria
collection PubMed
description Bacterial infections have attracted the attention of researchers in recent decades, especially due to the special problems they have faced, such as their increasing diversity and resistance to antibiotic treatment. The emergence and development of the SARS-CoV-2 infection stimulated even more research to find new structures with antimicrobial and antiviral properties. Among the heterocyclic compounds with remarkable therapeutic properties, benzimidazoles, and triazoles stand out, possessing antimicrobial, antiviral, antitumor, anti-Alzheimer, anti-inflammatory, analgesic, antidiabetic, or anti-ulcer activities. In addition, the literature of the last decade reports benzimidazole-triazole hybrids with improved biological properties compared to the properties of simple mono-heterocyclic compounds. This review aims to provide an update on the synthesis methods of these hybrids, along with their antimicrobial and antiviral activities, as well as the structure–activity relationship reported in the literature. It was found that the presence of certain groups grafted onto the benzimidazole and/or triazole nuclei (-F, -Cl, -Br, -CF(3), -NO(2), -CN, -CHO, -OH, OCH(3), COOCH(3)), as well as the presence of some heterocycles (pyridine, pyrimidine, thiazole, indole, isoxazole, thiadiazole, coumarin) increases the antimicrobial activity of benzimidazole-triazole hybrids. Also, the presence of the oxygen or sulfur atom in the bridge connecting the benzimidazole and triazole rings generally increases the antimicrobial activity of the hybrids. The literature mentions only benzimidazole-1,2,3-triazole hybrids with antiviral properties. Both for antimicrobial and antiviral hybrids, the presence of an additional triazole ring increases their biological activity, which is in agreement with the three-dimensional binding mode of compounds. This review summarizes the advances of benzimidazole triazole derivatives as potential antimicrobial and antiviral agents covering articles published from 2000 to 2023.
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spelling pubmed-103762512023-07-29 Benzimidazole-Triazole Hybrids as Antimicrobial and Antiviral Agents: A Systematic Review Marinescu, Maria Antibiotics (Basel) Review Bacterial infections have attracted the attention of researchers in recent decades, especially due to the special problems they have faced, such as their increasing diversity and resistance to antibiotic treatment. The emergence and development of the SARS-CoV-2 infection stimulated even more research to find new structures with antimicrobial and antiviral properties. Among the heterocyclic compounds with remarkable therapeutic properties, benzimidazoles, and triazoles stand out, possessing antimicrobial, antiviral, antitumor, anti-Alzheimer, anti-inflammatory, analgesic, antidiabetic, or anti-ulcer activities. In addition, the literature of the last decade reports benzimidazole-triazole hybrids with improved biological properties compared to the properties of simple mono-heterocyclic compounds. This review aims to provide an update on the synthesis methods of these hybrids, along with their antimicrobial and antiviral activities, as well as the structure–activity relationship reported in the literature. It was found that the presence of certain groups grafted onto the benzimidazole and/or triazole nuclei (-F, -Cl, -Br, -CF(3), -NO(2), -CN, -CHO, -OH, OCH(3), COOCH(3)), as well as the presence of some heterocycles (pyridine, pyrimidine, thiazole, indole, isoxazole, thiadiazole, coumarin) increases the antimicrobial activity of benzimidazole-triazole hybrids. Also, the presence of the oxygen or sulfur atom in the bridge connecting the benzimidazole and triazole rings generally increases the antimicrobial activity of the hybrids. The literature mentions only benzimidazole-1,2,3-triazole hybrids with antiviral properties. Both for antimicrobial and antiviral hybrids, the presence of an additional triazole ring increases their biological activity, which is in agreement with the three-dimensional binding mode of compounds. This review summarizes the advances of benzimidazole triazole derivatives as potential antimicrobial and antiviral agents covering articles published from 2000 to 2023. MDPI 2023-07-22 /pmc/articles/PMC10376251/ /pubmed/37508316 http://dx.doi.org/10.3390/antibiotics12071220 Text en © 2023 by the author. 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 Review
Marinescu, Maria
Benzimidazole-Triazole Hybrids as Antimicrobial and Antiviral Agents: A Systematic Review
title Benzimidazole-Triazole Hybrids as Antimicrobial and Antiviral Agents: A Systematic Review
title_full Benzimidazole-Triazole Hybrids as Antimicrobial and Antiviral Agents: A Systematic Review
title_fullStr Benzimidazole-Triazole Hybrids as Antimicrobial and Antiviral Agents: A Systematic Review
title_full_unstemmed Benzimidazole-Triazole Hybrids as Antimicrobial and Antiviral Agents: A Systematic Review
title_short Benzimidazole-Triazole Hybrids as Antimicrobial and Antiviral Agents: A Systematic Review
title_sort benzimidazole-triazole hybrids as antimicrobial and antiviral agents: a systematic review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10376251/
https://www.ncbi.nlm.nih.gov/pubmed/37508316
http://dx.doi.org/10.3390/antibiotics12071220
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