Antibacterial, antifungal and cytotoxic evaluation of some new 2,3-disubstituted 4(3H)-quinazolinone derivatives

In this study antibacterial, antifungal and cytotoxic effects of some new 2,3-disubstituted 4(3H)-quinazolinone derivatives have been evaluated. The in vitro antibacterial and antifungal tests of new synthesized compounds were performed using MABA method against six strains of bacteria (three Grampo...

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Published inResearch in pharmaceutical sciences Vol. 7; no. 3; pp. 151 - 158
Main Authors Khodarahmi, G A, Khajouei, M Rahmani, Hakimelahi, G H, Abedi, D, Jafari, E, Hassanzadeh, F
Format Journal Article
LanguageEnglish
Published Iran Medknow Publications & Media Pvt Ltd 01.07.2012
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Abstract In this study antibacterial, antifungal and cytotoxic effects of some new 2,3-disubstituted 4(3H)-quinazolinone derivatives have been evaluated. The in vitro antibacterial and antifungal tests of new synthesized compounds were performed using MABA method against six strains of bacteria (three Grampositive and three Gram-negative) and three strains of fungi. Also Minimum Bactericidal Concentration (MBC) and Minimum Fungicidal Concentration (MFC) tests were performed. All synthesized compounds indicated mild antibacterial effects especially against Gram-negative bacteria. The most sensitive bacteriumwas E. coli. All strains of tested fungi were sensitive to the synthesized compounds mostly at 32 μg/ml and there was no significant differences in the sensitivity of the tested compounds. MBC and MFC data indicated that tested compounds act as bactriostatic and fungistatic agents. Cytotoxic activity of the compounds was screened at 1, 10 and 100 μM concentrations against HeLa cells using the MTT colorimetric assay. While the synthesized compounds did not show significant cytotoxic activities, compounds 7a(3) and 7a(4) reduced cell viability to about 50% at 100 μM concentration. The present study revealed that most of the new synthesized compounds possess good antifungal effects and they could be considered as valuable candidates for further structural modification to design more potent antifungal agents.
AbstractList In this study antibacterial, antifungal and cytotoxic effects of some new 2,3-disubstituted 4(3H)-quinazolinone derivatives have been evaluated. The in vitro antibacterial and antifungal tests of new synthesized compounds were performed using MABA method against six strains of bacteria (three Grampositive and three Gram-negative) and three strains of fungi. Also Minimum Bactericidal Concentration (MBC) and Minimum Fungicidal Concentration (MFC) tests were performed. All synthesized compounds indicated mild antibacterial effects especially against Gram-negative bacteria. The most sensitive bacteriumwas E. coli. All strains of tested fungi were sensitive to the synthesized compounds mostly at 32 μg/ml and there was no significant differences in the sensitivity of the tested compounds. MBC and MFC data indicated that tested compounds act as bactriostatic and fungistatic agents. Cytotoxic activity of the compounds was screened at 1, 10 and 100 μM concentrations against HeLa cells using the MTT colorimetric assay. While the synthesized compounds did not show significant cytotoxic activities, compounds 7a(3) and 7a(4) reduced cell viability to about 50% at 100 μM concentration. The present study revealed that most of the new synthesized compounds possess good antifungal effects and they could be considered as valuable candidates for further structural modification to design more potent antifungal agents.
In this study antibacterial, antifungal and cytotoxic effects of some new 2,3-disubstituted 4(3H)-quinazolinone derivatives have been evaluated. The in vitro antibacterial and antifungal tests of new synthesized compounds were performed using MABA method against six strains of bacteria (three Grampositive and three Gram-negative) and three strains of fungi. Also Minimum Bactericidal Concentration (MBC) and Minimum Fungicidal Concentration (MFC) tests were performed. All synthesized compounds indicated mild antibacterial effects especially against Gram-negative bacteria. The most sensitive bacteriumwas E. coli . All strains of tested fungi were sensitive to the synthesized compounds mostly at 32 μg/ml and there was no significant differences in the sensitivity of the tested compounds. MBC and MFC data indicated that tested compounds act as bactriostatic and fungistatic agents. Cytotoxic activity of the compounds was screened at 1, 10 and 100 μM concentrations against HeLa cells using the MTT colorimetric assay. While the synthesized compounds did not show significant cytotoxic activities, compounds 7a 3 and 7a 4 reduced cell viability to about 50% at 100 μM concentration. The present study revealed that most of the new synthesized compounds possess good antifungal effects and they could be considered as valuable candidates for further structural modification to design more potent antifungal agents.
Author Khajouei, M Rahmani
Hassanzadeh, F
Jafari, E
Khodarahmi, G A
Hakimelahi, G H
Abedi, D
AuthorAffiliation 2 Isfahan Pharmaceutical Sciences Research Center, Isfahan, I.R.Iran
4 Department of Biotechnology and Isfahan Pharmaceutical Sciences Research Center, School of Pharmacy and Pharmaceutical Science, Isfahan University of Medical Sciences, Isfahan, I.R.Iran
1 Department of Medicinal Chemistry, School of Pharmacy and Pharmaceutical Science, Isfahan University of Medical Sciences, Isfahan, I.R.Iran
3 Institute of Chemistry, Academia Sinica, Nankang, Taipei, Taiwan
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Keywords Cytotoxicity
Antifungal
4(3H)-Quinazolinone
Antibacterial
Language English
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References 17978522 - Chem Pharm Bull (Tokyo). 2007 Nov;55(11):1615-9
20599299 - Eur J Med Chem. 2010 Sep;45(9):4188-98
6606682 - J Immunol Methods. 1983 Dec 16;65(1-2):55-63
21194809 - Eur J Med Chem. 2011 Feb;46(2):691-703
18614258 - Eur J Med Chem. 2009 Mar;44(3):1188-97
19541484 - Bioorg Med Chem Lett. 2009 Aug 1;19(15):4196-200
17962771 - Molecules. 2006;11(6):383-92
19109016 - Bioorg Med Chem Lett. 2009 Feb 1;19(3):800-2
10748620 - Pharm Acta Helv. 1999 Dec;74(1):11-7
2536729 - J Biol Chem. 1989 Feb 15;264(5):2973-8
17978766 - Molecules. 2007;12(10):2413-26
20350811 - Bioorg Med Chem. 2010 Apr 15;18(8):2849-63
12849729 - Toxicol In Vitro. 2003 Aug;17(4):457-63
23181076 - Res Pharm Sci. 2012 Jan;7(1):23-30
12951471 - Biol Pharm Bull. 2003 Sep;26(9):1278-82
15780632 - Bioorg Med Chem Lett. 2005 Apr 1;15(7):1915-7
15733846 - FEBS Lett. 2005 Feb 28;579(6):1389-93
15072839 - Eur J Med Chem. 2004 Apr;39(4):299-304
8567901 - J Clin Microbiol. 1995 Oct;33(10):2660-4
20510483 - Eur J Med Chem. 2010 Aug;45(8):3365-73
2549608 - Rev Infect Dis. 1989 Jul-Aug;11 Suppl 5:S902-11
17981366 - Eur J Med Chem. 2008 Jul;43(7):1478-88
18603337 - Eur J Med Chem. 2009 May;44(5):2328-33
11354375 - Bioorg Med Chem Lett. 2001 May 7;11(9):1193-6
8897159 - J Clin Microbiol. 1996 Nov;34(11):2654-9
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Title Antibacterial, antifungal and cytotoxic evaluation of some new 2,3-disubstituted 4(3H)-quinazolinone derivatives
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