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Microbiological Evaluation of 4-substituted-imidazolidine Derivatives
In the present studies, two series of 4-substituted-imidazolidines (IIIa-i and IIIj,k) were synthesized by reacting different tetrahydro-di-Schiff bases (IIa-i and IIj,k) with p-diethylaminobenzaldehyde/ dimethylaminobenzaldehyde. The title compounds were evaluated for their antibacterial and antifu...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507351/ https://www.ncbi.nlm.nih.gov/pubmed/23204628 http://dx.doi.org/10.4103/0250-474X.102549 |
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author | Khan, M. S. Y. Husain, A. Sharma, S. Rashid, M. |
author_facet | Khan, M. S. Y. Husain, A. Sharma, S. Rashid, M. |
author_sort | Khan, M. S. Y. |
collection | PubMed |
description | In the present studies, two series of 4-substituted-imidazolidines (IIIa-i and IIIj,k) were synthesized by reacting different tetrahydro-di-Schiff bases (IIa-i and IIj,k) with p-diethylaminobenzaldehyde/ dimethylaminobenzaldehyde. The title compounds were evaluated for their antibacterial and antifungal actions against some selected microbes. The results of microbiological evaluation revealed that two compounds, 4-(1,3-bis(benzo[d][1,3]dioxol-5-ylmethyl)-4-methylimidazolidin-2-yl)-N,N-diethyl aniline (IIIj), 4-(1,3-bis(benzo[d][1,3]dioxol-5-ylmethyl)-4-methylimidazolidin-2-yl)-N,N-dimethyl aniline (IIIk) were good in their antibacterial as well as antifungal actions. Minimum inhibitory concentration values (MIC) of the compounds are reported. |
format | Online Article Text |
id | pubmed-3507351 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35073512012-11-30 Microbiological Evaluation of 4-substituted-imidazolidine Derivatives Khan, M. S. Y. Husain, A. Sharma, S. Rashid, M. Indian J Pharm Sci Short Communication In the present studies, two series of 4-substituted-imidazolidines (IIIa-i and IIIj,k) were synthesized by reacting different tetrahydro-di-Schiff bases (IIa-i and IIj,k) with p-diethylaminobenzaldehyde/ dimethylaminobenzaldehyde. The title compounds were evaluated for their antibacterial and antifungal actions against some selected microbes. The results of microbiological evaluation revealed that two compounds, 4-(1,3-bis(benzo[d][1,3]dioxol-5-ylmethyl)-4-methylimidazolidin-2-yl)-N,N-diethyl aniline (IIIj), 4-(1,3-bis(benzo[d][1,3]dioxol-5-ylmethyl)-4-methylimidazolidin-2-yl)-N,N-dimethyl aniline (IIIk) were good in their antibacterial as well as antifungal actions. Minimum inhibitory concentration values (MIC) of the compounds are reported. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3507351/ /pubmed/23204628 http://dx.doi.org/10.4103/0250-474X.102549 Text en Copyright: © Indian Journal of Pharmaceutical Sciences http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Communication Khan, M. S. Y. Husain, A. Sharma, S. Rashid, M. Microbiological Evaluation of 4-substituted-imidazolidine Derivatives |
title | Microbiological Evaluation of 4-substituted-imidazolidine Derivatives |
title_full | Microbiological Evaluation of 4-substituted-imidazolidine Derivatives |
title_fullStr | Microbiological Evaluation of 4-substituted-imidazolidine Derivatives |
title_full_unstemmed | Microbiological Evaluation of 4-substituted-imidazolidine Derivatives |
title_short | Microbiological Evaluation of 4-substituted-imidazolidine Derivatives |
title_sort | microbiological evaluation of 4-substituted-imidazolidine derivatives |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3507351/ https://www.ncbi.nlm.nih.gov/pubmed/23204628 http://dx.doi.org/10.4103/0250-474X.102549 |
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