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Antimicrobial evaluation of some novel derivatives of 3,4-dihydropyrimidine-2(1H)-one

The antimicrobial activity of thirty six novel dihydropyrimidine derivatives was evaluated against common pathogenic bacteria. Significant antimicrobial activity (MIC=32, 64 μg/ml) was observed. Escherichia coli and Pseudomonas aeruginosa as Gram-negative bacteria and Staphylococcus aureus as Gram-p...

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Autores principales: Jalali, M., Mahdavi, M., Memarian, H.R., Ranjbar, M., Soleymani, M., Fassihi, A., Abedi, D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523416/
https://www.ncbi.nlm.nih.gov/pubmed/23248675
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author Jalali, M.
Mahdavi, M.
Memarian, H.R.
Ranjbar, M.
Soleymani, M.
Fassihi, A.
Abedi, D.
author_facet Jalali, M.
Mahdavi, M.
Memarian, H.R.
Ranjbar, M.
Soleymani, M.
Fassihi, A.
Abedi, D.
author_sort Jalali, M.
collection PubMed
description The antimicrobial activity of thirty six novel dihydropyrimidine derivatives was evaluated against common pathogenic bacteria. Significant antimicrobial activity (MIC=32, 64 μg/ml) was observed. Escherichia coli and Pseudomonas aeruginosa as Gram-negative bacteria and Staphylococcus aureus as Gram-positive bacteria were determined to be the most susceptible pathogens in this study. The highest inhibitory activity was observed against Gram-negative microorganisms. The widest spectrum of antibacterial activity was exerted by C6 and C22. Most of the compounds had remarkable antifungal activity (MIC=32 μg/ml).
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spelling pubmed-35234162012-12-17 Antimicrobial evaluation of some novel derivatives of 3,4-dihydropyrimidine-2(1H)-one Jalali, M. Mahdavi, M. Memarian, H.R. Ranjbar, M. Soleymani, M. Fassihi, A. Abedi, D. Res Pharm Sci Original Article The antimicrobial activity of thirty six novel dihydropyrimidine derivatives was evaluated against common pathogenic bacteria. Significant antimicrobial activity (MIC=32, 64 μg/ml) was observed. Escherichia coli and Pseudomonas aeruginosa as Gram-negative bacteria and Staphylococcus aureus as Gram-positive bacteria were determined to be the most susceptible pathogens in this study. The highest inhibitory activity was observed against Gram-negative microorganisms. The widest spectrum of antibacterial activity was exerted by C6 and C22. Most of the compounds had remarkable antifungal activity (MIC=32 μg/ml). Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3523416/ /pubmed/23248675 Text en Copyright: © Journal of Research in 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 Original Article
Jalali, M.
Mahdavi, M.
Memarian, H.R.
Ranjbar, M.
Soleymani, M.
Fassihi, A.
Abedi, D.
Antimicrobial evaluation of some novel derivatives of 3,4-dihydropyrimidine-2(1H)-one
title Antimicrobial evaluation of some novel derivatives of 3,4-dihydropyrimidine-2(1H)-one
title_full Antimicrobial evaluation of some novel derivatives of 3,4-dihydropyrimidine-2(1H)-one
title_fullStr Antimicrobial evaluation of some novel derivatives of 3,4-dihydropyrimidine-2(1H)-one
title_full_unstemmed Antimicrobial evaluation of some novel derivatives of 3,4-dihydropyrimidine-2(1H)-one
title_short Antimicrobial evaluation of some novel derivatives of 3,4-dihydropyrimidine-2(1H)-one
title_sort antimicrobial evaluation of some novel derivatives of 3,4-dihydropyrimidine-2(1h)-one
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3523416/
https://www.ncbi.nlm.nih.gov/pubmed/23248675
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