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新型DNA回旋酶抑制剂ABT-719的体外评估

In vitro evaluation of ABT-719, a novel DNA gyrase inhibitor.

作者信息

Flamm R K, Vojtko C, Chu D T, Li Q, Beyer J, Hensey D, Ramer N, Clement J J, Tanaka S K

机构信息

Department 47T, Abbott Laboratories, Abbott Park, Illinois 60064-3500, USA.

出版信息

Antimicrob Agents Chemother. 1995 Apr;39(4):964-70. doi: 10.1128/AAC.39.4.964.

Abstract

ABT-719 (A-86719.1) is the first compound of a new class of novel DNA gyrase inhibitors, the 2-pyridones, with potent antibacterial activity against gram-positive, gram-negative, and anaerobic organisms. ABT-719 was more active than ciprofloxacin, sparfloxacin, and clinafloxacin against gram-positive bacteria. ABT-719 was particularly active against Staphylococcus aureus (MIC at which 90% of the isolates were inhibited [MIC90] = 0.015 micrograms/ml) and Streptococcus pneumoniae (MIC90 = 0.03 micrograms/ml). ABT-719 was also the most active of the compounds tested against ciprofloxacin-resistant S. aureus isolates, with an MIC90 of 0.25 micrograms/ml, compared with 64 micrograms/ml for ciprofloxacin. Against gram-negative organisms, ABT-719 was as active as or slightly more active than ciprofloxacin and was the most active compound against ciprofloxacin-resistant Pseudomonas aeruginosa (MIC90 = 2.0 micrograms/ml). ABT-719 was also the most active compound against both gram-positive and gram-negative anaerobes, with MIC90s ranging from 0.12 to 0.25 micrograms/ml.

摘要

ABT - 719(A - 86719.1)是新型DNA促旋酶抑制剂(2 - 吡啶酮类)中的首个化合物,对革兰氏阳性菌、革兰氏阴性菌及厌氧菌具有强大的抗菌活性。ABT - 719对革兰氏阳性菌的活性高于环丙沙星、司帕沙星和克林沙星。ABT - 719对金黄色葡萄球菌(90%分离株被抑制时的最低抑菌浓度[MIC90]=0.015微克/毫升)和肺炎链球菌(MIC90 = 0.03微克/毫升)尤其具有活性。ABT - 719也是所测试化合物中对耐环丙沙星金黄色葡萄球菌分离株活性最强的,其MIC90为0.25微克/毫升,而环丙沙星的MIC90为64微克/毫升。对于革兰氏阴性菌,ABT - 719的活性与环丙沙星相当或略高于环丙沙星,并且是对耐环丙沙星铜绿假单胞菌活性最强的化合物(MIC90 = 2.0微克/毫升)。ABT - 719也是对革兰氏阳性和革兰氏阴性厌氧菌活性最强的化合物,其MIC90范围为0.12至0.25微克/毫升。

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