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Synthesis and Antimicrobial Activity of 5-Imidazolinone Derivatives
Several 4-arylidene-2-phenyl-1-(2,4,5-trichlorophenyl)-1H-imidazol-5(4H)-ones (4a-q), N-(4-benzylidene-5-oxo-2-phenyl-4,5-dihydroimidazol-1-yl)-4-chlorobenzamides (5a-o) and N-(4-benzylidene-5-oxo-2-phenyl-4,5-dihydroimidazol-1-yl)-2,4-dichlorobenzamides (6a-m) were prepared. All newly synthesized c...
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Formato: | Texto |
Lenguaje: | English |
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Medknow Publications
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2810063/ https://www.ncbi.nlm.nih.gov/pubmed/20177470 http://dx.doi.org/10.4103/0250-474X.51953 |
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author | Desai, N. C. Bhavsar, A. M. Baldaniya, B. B. |
author_facet | Desai, N. C. Bhavsar, A. M. Baldaniya, B. B. |
author_sort | Desai, N. C. |
collection | PubMed |
description | Several 4-arylidene-2-phenyl-1-(2,4,5-trichlorophenyl)-1H-imidazol-5(4H)-ones (4a-q), N-(4-benzylidene-5-oxo-2-phenyl-4,5-dihydroimidazol-1-yl)-4-chlorobenzamides (5a-o) and N-(4-benzylidene-5-oxo-2-phenyl-4,5-dihydroimidazol-1-yl)-2,4-dichlorobenzamides (6a-m) were prepared. All newly synthesized compounds have been tested for their antibacterial activity against gram (+)ve and gram (−)ve bacteria and also on different strains of fungi. Introduction of OH, OCH(3), NO(2), Cl and Br groups to the heterocyclic frame work enhanced antibacterial and antifungal activities. |
format | Text |
id | pubmed-2810063 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Medknow Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-28100632010-02-22 Synthesis and Antimicrobial Activity of 5-Imidazolinone Derivatives Desai, N. C. Bhavsar, A. M. Baldaniya, B. B. Indian J Pharm Sci Short Communication Several 4-arylidene-2-phenyl-1-(2,4,5-trichlorophenyl)-1H-imidazol-5(4H)-ones (4a-q), N-(4-benzylidene-5-oxo-2-phenyl-4,5-dihydroimidazol-1-yl)-4-chlorobenzamides (5a-o) and N-(4-benzylidene-5-oxo-2-phenyl-4,5-dihydroimidazol-1-yl)-2,4-dichlorobenzamides (6a-m) were prepared. All newly synthesized compounds have been tested for their antibacterial activity against gram (+)ve and gram (−)ve bacteria and also on different strains of fungi. Introduction of OH, OCH(3), NO(2), Cl and Br groups to the heterocyclic frame work enhanced antibacterial and antifungal activities. Medknow Publications 2009 /pmc/articles/PMC2810063/ /pubmed/20177470 http://dx.doi.org/10.4103/0250-474X.51953 Text en © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Desai, N. C. Bhavsar, A. M. Baldaniya, B. B. Synthesis and Antimicrobial Activity of 5-Imidazolinone Derivatives |
title | Synthesis and Antimicrobial Activity of 5-Imidazolinone Derivatives |
title_full | Synthesis and Antimicrobial Activity of 5-Imidazolinone Derivatives |
title_fullStr | Synthesis and Antimicrobial Activity of 5-Imidazolinone Derivatives |
title_full_unstemmed | Synthesis and Antimicrobial Activity of 5-Imidazolinone Derivatives |
title_short | Synthesis and Antimicrobial Activity of 5-Imidazolinone Derivatives |
title_sort | synthesis and antimicrobial activity of 5-imidazolinone derivatives |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2810063/ https://www.ncbi.nlm.nih.gov/pubmed/20177470 http://dx.doi.org/10.4103/0250-474X.51953 |
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