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恶唑烷酮类药物RWJ-416457对耐利奈唑胺和对利奈唑胺敏感的葡萄球菌及肠球菌的体外活性

In vitro activity of the oxazolidinone RWJ-416457 against linezolid-resistant and -susceptible staphylococci and enterococci.

作者信息

Livermore David M, Warner Marina, Mushtaq Shazad, North Sarah, Woodford Neil

机构信息

Antibiotic Resistance Monitoring and Reference Laboratory, Health Protection Agency Centre for Infections, 61 Colindale Avenue, London NW9 5EQ, United Kingdom.

出版信息

Antimicrob Agents Chemother. 2007 Mar;51(3):1112-4. doi: 10.1128/AAC.01347-06. Epub 2007 Jan 8.

DOI:10.1128/AAC.01347-06
PMID:17210773
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1803128/
Abstract

RWJ-416457, a novel oxazolidinone, had modal MICs of 0.5 to 1 microg/ml for linezolid-susceptible staphylococci and enterococci, versus linezolid MICs for these organisms of 1 or 2 microg/ml. RWJ-416457 MICs for mutants with 23S rRNA mutations were 2 to 32 microg/ml, versus linezolid MICs of 8 to 64 microg/ml; actual values reflected the proportion of gene copies mutated.

摘要

新型恶唑烷酮类药物RWJ - 416457对利奈唑胺敏感的葡萄球菌和肠球菌的最低抑菌浓度(MIC)范围为0.5至1微克/毫升,而这些菌株对利奈唑胺的MIC为1或2微克/毫升。对于具有23S rRNA突变的突变体,RWJ - 416457的MIC为2至32微克/毫升,而利奈唑胺的MIC为8至64微克/毫升;实际数值反映了发生突变的基因拷贝比例。

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In vitro antibacterial activity of the pyrrolopyrazolyl-substituted oxazolidinone RWJ-416457.吡咯并吡唑基取代恶唑烷酮RWJ-416457的体外抗菌活性
Antimicrob Agents Chemother. 2007 Jan;51(1):361-5. doi: 10.1128/AAC.01017-06. Epub 2006 Nov 13.
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Linezolid versus vancomycin in treatment of complicated skin and soft tissue infections.利奈唑胺与万古霉素治疗复杂性皮肤及软组织感染的比较
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Linezolid vs vancomycin: analysis of two double-blind studies of patients with methicillin-resistant Staphylococcus aureus nosocomial pneumonia.利奈唑胺与万古霉素对比:耐甲氧西林金黄色葡萄球菌医院获得性肺炎患者两项双盲研究的分析
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