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4-[1-(Substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzenesulfonic acids: Synthesis, antimicrobial activity, QSAR studies, and antiviral evaluation

A series of 4-[1-(substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzene sulphonic acids (1-20) was synthesized and evaluated, in vitro, for their antimicrobial activity and the results indicated that compounds 4-[1-(4-Nitrobenzoyl)-1H-benzoimidazol-2-yl]-benzenesulfonic acid (9) and 4-(1-octa...

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Autores principales: Yadav, Snehlata, Kumar, Pradeep, De Clercq, Erik, Balzarini, Jan, Pannecouque, Christophe, Dewan, Sharwan Kumar, Narasimhan, Balasubramanian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Masson SAS. 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115694/
https://www.ncbi.nlm.nih.gov/pubmed/20971531
http://dx.doi.org/10.1016/j.ejmech.2010.09.065
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author Yadav, Snehlata
Kumar, Pradeep
De Clercq, Erik
Balzarini, Jan
Pannecouque, Christophe
Dewan, Sharwan Kumar
Narasimhan, Balasubramanian
author_facet Yadav, Snehlata
Kumar, Pradeep
De Clercq, Erik
Balzarini, Jan
Pannecouque, Christophe
Dewan, Sharwan Kumar
Narasimhan, Balasubramanian
author_sort Yadav, Snehlata
collection PubMed
description A series of 4-[1-(substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzene sulphonic acids (1-20) was synthesized and evaluated, in vitro, for their antimicrobial activity and the results indicated that compounds 4-[1-(4-Nitrobenzoyl)-1H-benzoimidazol-2-yl]-benzenesulfonic acid (9) and 4-(1-octadec-9-enoyl-1H-benzoimidazol-2-yl)-benzenesulfonic acid (18) were found to be the most active ones. QSAR investigations indicated that the multi-target QSAR model was effective in describing the antimicrobial activity over the one-target QSAR models. Further the mt-QSAR model indicated the importance of the topological parameter, Balaban index (J) followed by the electronic parameter, LUMO and topological parameter, valence second order molecular connectivity index ((2)χ(v)) in describing the antimicrobial activity of synthesized compounds (1-20).
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spelling pubmed-71156942020-04-02 4-[1-(Substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzenesulfonic acids: Synthesis, antimicrobial activity, QSAR studies, and antiviral evaluation Yadav, Snehlata Kumar, Pradeep De Clercq, Erik Balzarini, Jan Pannecouque, Christophe Dewan, Sharwan Kumar Narasimhan, Balasubramanian Eur J Med Chem Original Article A series of 4-[1-(substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzene sulphonic acids (1-20) was synthesized and evaluated, in vitro, for their antimicrobial activity and the results indicated that compounds 4-[1-(4-Nitrobenzoyl)-1H-benzoimidazol-2-yl]-benzenesulfonic acid (9) and 4-(1-octadec-9-enoyl-1H-benzoimidazol-2-yl)-benzenesulfonic acid (18) were found to be the most active ones. QSAR investigations indicated that the multi-target QSAR model was effective in describing the antimicrobial activity over the one-target QSAR models. Further the mt-QSAR model indicated the importance of the topological parameter, Balaban index (J) followed by the electronic parameter, LUMO and topological parameter, valence second order molecular connectivity index ((2)χ(v)) in describing the antimicrobial activity of synthesized compounds (1-20). Elsevier Masson SAS. 2010-12 2010-10-07 /pmc/articles/PMC7115694/ /pubmed/20971531 http://dx.doi.org/10.1016/j.ejmech.2010.09.065 Text en Copyright © 2010 Elsevier Masson SAS. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Original Article
Yadav, Snehlata
Kumar, Pradeep
De Clercq, Erik
Balzarini, Jan
Pannecouque, Christophe
Dewan, Sharwan Kumar
Narasimhan, Balasubramanian
4-[1-(Substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzenesulfonic acids: Synthesis, antimicrobial activity, QSAR studies, and antiviral evaluation
title 4-[1-(Substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzenesulfonic acids: Synthesis, antimicrobial activity, QSAR studies, and antiviral evaluation
title_full 4-[1-(Substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzenesulfonic acids: Synthesis, antimicrobial activity, QSAR studies, and antiviral evaluation
title_fullStr 4-[1-(Substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzenesulfonic acids: Synthesis, antimicrobial activity, QSAR studies, and antiviral evaluation
title_full_unstemmed 4-[1-(Substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzenesulfonic acids: Synthesis, antimicrobial activity, QSAR studies, and antiviral evaluation
title_short 4-[1-(Substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzenesulfonic acids: Synthesis, antimicrobial activity, QSAR studies, and antiviral evaluation
title_sort 4-[1-(substituted aryl/alkyl carbonyl)-benzoimidazol-2-yl]-benzenesulfonic acids: synthesis, antimicrobial activity, qsar studies, and antiviral evaluation
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7115694/
https://www.ncbi.nlm.nih.gov/pubmed/20971531
http://dx.doi.org/10.1016/j.ejmech.2010.09.065
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