Abstract
Some benzimidazole derivatives bearing hydrazone moiety were synthesized and their in vitro antimicrobial activity was determined against various gram-positive and gram-negative bacteria, and fungi using microbroth dilution method. The structures of all new compounds were identified by1H-NMR, FT-IR, MS spectroscopic techniques and elemental analysis. Sixteen final products were examined for their in vitro antimicrobial activities. When compared to the reference agents, chloramphenicol and ketoconazole, most of the synthesized compounds showed sufficient antibacterial activity against Pseudomonas aeruginosa and antifungal activity against Candida albicans and C. glabrata.
Keywords: Benzimidazole, Hydrazone, Antibacterial activity, Antifungal activity.
Letters in Drug Design & Discovery
Title:Synthesis and Antimicrobial Evaluation of Some 2,5-Disubstituted Benzimidazole Derivatives
Volume: 10 Issue: 6
Author(s): Leyla Yurttas, Yusuf Ozkay, Hulya Karaca, Yagmur Tunali and Zafer Asim Kaplancıkli
Affiliation:
Keywords: Benzimidazole, Hydrazone, Antibacterial activity, Antifungal activity.
Abstract: Some benzimidazole derivatives bearing hydrazone moiety were synthesized and their in vitro antimicrobial activity was determined against various gram-positive and gram-negative bacteria, and fungi using microbroth dilution method. The structures of all new compounds were identified by1H-NMR, FT-IR, MS spectroscopic techniques and elemental analysis. Sixteen final products were examined for their in vitro antimicrobial activities. When compared to the reference agents, chloramphenicol and ketoconazole, most of the synthesized compounds showed sufficient antibacterial activity against Pseudomonas aeruginosa and antifungal activity against Candida albicans and C. glabrata.
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Cite this article as:
Yurttas Leyla, Ozkay Yusuf, Karaca Hulya, Tunali Yagmur and Kaplancıkli Zafer Asim, Synthesis and Antimicrobial Evaluation of Some 2,5-Disubstituted Benzimidazole Derivatives, Letters in Drug Design & Discovery 2013; 10(6) . https://dx.doi.org/10.2174/1570180811310060003
DOI https://dx.doi.org/10.2174/1570180811310060003 |
Print ISSN 1570-1808 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-628X |

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