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Antibacterial, antifungal and cytotoxic evaluation of some new quinazolinone derivatives

Quinazolinone ring system is renown because of its wide spectrum of pharmacological activities due to various substitutions on this ring system. In this study, the minimum inhibitory concentration of the synthesized compounds in our laboratory was determined by micro dilution Alamar Blue(®) Assay ag...

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Autores principales: Hassanzadeh, F., Jafari, E., Hakimelahi, G.H., Khajouei, M. Rahmani, Jalali, M., Khodarahmi, G.A.
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/PMC3501904/
https://www.ncbi.nlm.nih.gov/pubmed/23181085
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author Hassanzadeh, F.
Jafari, E.
Hakimelahi, G.H.
Khajouei, M. Rahmani
Jalali, M.
Khodarahmi, G.A.
author_facet Hassanzadeh, F.
Jafari, E.
Hakimelahi, G.H.
Khajouei, M. Rahmani
Jalali, M.
Khodarahmi, G.A.
author_sort Hassanzadeh, F.
collection PubMed
description Quinazolinone ring system is renown because of its wide spectrum of pharmacological activities due to various substitutions on this ring system. In this study, the minimum inhibitory concentration of the synthesized compounds in our laboratory was determined by micro dilution Alamar Blue(®) Assay against six strains of bacteria (three Gram-positive and three Gram-negative) and three strains of fungi. Following a broth micro dilution minimum inhibitory concentration (MIC) test, Minimum Bactericidal Concentration (MBC) and Minimum Fungicidal Concentration (MFC) tests were performed. Cytotoxic effects of the compounds were measured using the MTT colorimetric assay on HeLa cell line. Results of antimicrobial screening showed that compounds had better bacteriostatic activity against Gram-negative bacteria. Results from MBC revealed that these compounds had more significant bacteriostatic than bactericidal activities. Nearly all screened compounds showed good activity against C. albicans and A. niger. Results from MFC indicated that these compounds had better fungistatic rather than fungicidal activities. The synthesized target molecules were found to exhibit different cytotoxicity in the range of 10 to 100 μM on HeLa cell line. Compounds 6 and 7 exhibited acceptable cytotoxicity approximately 50% at 10 μM concentration.
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spelling pubmed-35019042012-11-23 Antibacterial, antifungal and cytotoxic evaluation of some new quinazolinone derivatives Hassanzadeh, F. Jafari, E. Hakimelahi, G.H. Khajouei, M. Rahmani Jalali, M. Khodarahmi, G.A. Res Pharm Sci Original Article Quinazolinone ring system is renown because of its wide spectrum of pharmacological activities due to various substitutions on this ring system. In this study, the minimum inhibitory concentration of the synthesized compounds in our laboratory was determined by micro dilution Alamar Blue(®) Assay against six strains of bacteria (three Gram-positive and three Gram-negative) and three strains of fungi. Following a broth micro dilution minimum inhibitory concentration (MIC) test, Minimum Bactericidal Concentration (MBC) and Minimum Fungicidal Concentration (MFC) tests were performed. Cytotoxic effects of the compounds were measured using the MTT colorimetric assay on HeLa cell line. Results of antimicrobial screening showed that compounds had better bacteriostatic activity against Gram-negative bacteria. Results from MBC revealed that these compounds had more significant bacteriostatic than bactericidal activities. Nearly all screened compounds showed good activity against C. albicans and A. niger. Results from MFC indicated that these compounds had better fungistatic rather than fungicidal activities. The synthesized target molecules were found to exhibit different cytotoxicity in the range of 10 to 100 μM on HeLa cell line. Compounds 6 and 7 exhibited acceptable cytotoxicity approximately 50% at 10 μM concentration. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3501904/ /pubmed/23181085 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
Hassanzadeh, F.
Jafari, E.
Hakimelahi, G.H.
Khajouei, M. Rahmani
Jalali, M.
Khodarahmi, G.A.
Antibacterial, antifungal and cytotoxic evaluation of some new quinazolinone derivatives
title Antibacterial, antifungal and cytotoxic evaluation of some new quinazolinone derivatives
title_full Antibacterial, antifungal and cytotoxic evaluation of some new quinazolinone derivatives
title_fullStr Antibacterial, antifungal and cytotoxic evaluation of some new quinazolinone derivatives
title_full_unstemmed Antibacterial, antifungal and cytotoxic evaluation of some new quinazolinone derivatives
title_short Antibacterial, antifungal and cytotoxic evaluation of some new quinazolinone derivatives
title_sort antibacterial, antifungal and cytotoxic evaluation of some new quinazolinone derivatives
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3501904/
https://www.ncbi.nlm.nih.gov/pubmed/23181085
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