Inhibitors of DNA polymerase III as novel antimicrobial agents against gram-positive eubacteria

被引:32
作者
Tarantino, PM [1 ]
Zhi, CX [1 ]
Wright, GE [1 ]
Brown, NC [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Pharmacol & Mol Toxicol, Worcester, MA 01655 USA
关键词
D O I
10.1128/AAC.43.8.1982
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
6-Anilinouracils are selective inhibitors of DNA polymerase III, the enzyme required for the replication of chromosomal DNA in gram-positive bacteria (N. C. Brown, L, W. Dudycz, and G. E. Wright, Drugs Exp. Clin, Res. 12:555-564, 1986), A new class of 6-anilinouracils based on N-3 alkyl substitution of the uracil ring was synthesized and analyzed for activity as inhibitors of the gram-positive bacterial DNA polymerase III and the growth of gram-positive bacterial pathogens, Favorable in vitro properties of N-3-alkyl derivatives prompted the synthesis of derivatives in which the R group at N-3 was replaced with more-hydrophilic methoxyalkyl. and hydroxyalkyl groups. These hydroxyalkyl and methoxyalkyl derivatives displayed Ki values in the range from 0.4 to 2.8 mu M against relevant gram-positive bacterial DNA polymerase IIIs and antimicrobial activity with MICs in the range from 0.5 to 15 mu g/ml against a broad spectrum of gram-positive bacteria, including methicillin-resistant staphylococci and vancomycin-resistant enterococci, Two of these hydrophilic derivatives displayed protective activity in a simple mouse model of lethal staphylococcal infection.
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页码:1982 / 1987
页数:6
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