Exploration of Structure-Based on Imidazole Core as Antibacterial Agents

Author(s): Yong-Tao Duan, Zhong-Chang Wang, Ya-Li Sang, Xiang-Xiang Tao, Hai-Liang Zhu

Journal Name: Current Topics in Medicinal Chemistry

Volume 13 , Issue 24 , 2013


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Abstract:

Imidazole, a five-membered heterocycle having three carbon atoms, and two double bonds, having efficient antibacterial Escherichia coli, Bacillus subtili, Bacillus proteus, Staphylococcus aureus, Pseudomonas aeruginosa, and Helicobacter pyloriurease etc, shows a broad-spectrum of antibacterial activities. To Search new antibacterial drugs to overcome resistance of microorganisms to antibiotics, to date hundreds of this sort of derivatives have been synthesized and possess potent antibacterial activity. As the structure of imidazole derivatives is various, the target of antibacterial is also diverse including β-Lactamases, β-ketoacyl-acyl carrier protein synthase III (FabH), DNA gyrase and topoisomerase, glutamate racemase and urease. In this review, we will discuss the emergence of resistance to antibiotics and attempt to summarize the main developments of imidazole derivatives in the past ten years. We hope that increasing knowledge of the structure-activity relationship (SAR) will be beneficial to the rational design of new generation of small molecule antibacterial drugs.

Keywords: Antibacterial activity; antibacterial agents; docking; imidazole; kinase inhibitor; QSAR ; resistance to antibiotics; structure-activity relationship.

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Article Details

VOLUME: 13
ISSUE: 24
Year: 2013
Page: [3118 - 3130]
Pages: 13
DOI: 10.2174/15680266113136660222
Price: $65

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