Bacterial fatty acid biosynthesis: Targets for antibacterial drug discovery

被引:418
作者
Campbell, JW
Cronan, JE
机构
[1] Univ Illinois, Dept Microbiol, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
关键词
triclosan; cerulenin; thiolactomycin; isoniazid; diazoborine;
D O I
10.1146/annurev.micro.55.1.305
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The increase in drug-resistant pathogenic bacteria has created an urgent demand for new antibiotics. Among the more attractive targets for the development of new antibacterial compounds are the enzymes of fatty acid biosynthesis. Although a number of potent inhibitors of microbial fatty acid biosynthesis have been discovered, few of these are clinically useful drugs. Several of these fatty acid biosynthesis inhibitors have potential as lead compounds in the development of new antibacterials. This review encompasses the known inhibitors and prospective targets for new antibacterials.
引用
收藏
页码:305 / 332
页数:28
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