Protective properties of five newly synthesized cyclic compounds against sodium azide and N-methyl-N'-nitro-N-nitrosoguanidine genotoxicity

Turhan, K; Ozturkcan, SA; Turgut, Z; Karadayi, M; Gulluce, M

HERO ID

1450090

Reference Type

Journal Article

Year

2012

HERO ID 1450090
In Press No
Year 2012
Title Protective properties of five newly synthesized cyclic compounds against sodium azide and N-methyl-N'-nitro-N-nitrosoguanidine genotoxicity
Authors Turhan, K; Ozturkcan, SA; Turgut, Z; Karadayi, M; Gulluce, M
Journal Toxicology and Industrial Health
Volume 28
Issue 7 (Aug 2012)
Page Numbers 605-613
Abstract The current study aims to determine the antimutagenic potential of five newly synthesized cyclic compounds against the genotoxic agents sodium azide (NaN3) and N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). The mutant bacterial tester strains were NaN3-sensitive Salmonella typhimurium TA1535 and MNNG-sensitive Escherichia coli WP2uvrA. According to the results, all the test compounds showed significant antimutagenic activity. The inhibition rates ranged from 26.05% (Compound 4--1 μg/plate) to 68.54% (Compound 5--0.01 μg/plate) for NaN3 and from 32.44% (Compound 3--1 μg/plate) to 60.77% (Compound 5--1 μg/plate) for MNNG genotoxicity. Moreover, the mutagenic potential of the test compounds was investigated using the same strains. The results showed that all the test compounds do not have mutagenic potential on the bacterial strains at the tested concentrations. Thus, the findings of the present study give valuable information about chemical prevention from NaN3 and MNNG genotoxicity. [PUBLICATION ABSTRACT] The current study aims to determine the antimutagenic potential of five newly synthesized cyclic compounds against the genotoxic agents sodium azide (NaN) and N-methyl-N'-nitro-N-nitrosoguanidine (MNNG). The mutant bacterial tester strains were NaN-sensitive Salmonella typhimurium TA1535 and MNNG-sensitive Escherichia coli WP2uvrA. According to the results, all the test compounds showed significant antimutagenic activity. The inhibition rates ranged from 26.05% (Compound 4-1 μg/plate) to 68.54% (Compound 5-0.01 μg/plate) for NaN and from 32.44% (Compound 3-1 μg/plate) to 60.77% (Compound 5-1 μg/plate) for MNNG genotoxicity. Moreover, the mutagenic potential of the test compounds was investigated using the same strains. The results showed that all the test compounds do not have mutagenic potential on the bacterial strains at the tested concentrations. Thus, the findings of the present study give valuable information about chemical prevention from NaN and MNNG genotoxicity.
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