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714. Analysis of the Effect of Urine on the In Vitro Activity of Gepotidacin and Levofloxacin Against Escherichia coli Staphylococcus epidermidis and Staphylococcus saprophyticus

机译:714.尿液对Gepotidacin和左氧氟沙星对大肠杆菌表皮葡萄球菌和腐生葡萄球菌体外活性的影响分析

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摘要

BackgroundGepotidacin (GSK2140944) is a first in class novel triazaacenaphthylene bacterial type II topoisomerase inhibitor in clinical development for the treatment of gonorrhea and uncomplicated UTI (acute cystitis). Gepotidacin selectively inhibits bacterial DNA gyrase and topoisomerase IV by a unique mechanism not utilized by any currently approved therapeutic agent and demonstrates in vitro activity against most target pathogens resistant to established antibacterials, including fluoroquinolones. This study was undertaken to determine the effect of various urine parameters on the in vitro activity of gepotidacin and a comparative agent, levofloxacin, against a variety of bacteria.
机译:背景Gepotidacin(GSK2140944)是临床上开发的新型新颖的三氮杂ph烯细菌II型拓扑异构酶抑制剂,用于治疗淋病和单纯性UTI(急性膀胱炎)。吉普达霉素通过目前未获批准的任何治疗剂未利用的独特机制选择性抑制细菌DNA促旋酶和拓扑异构酶IV,并证明了其对大多数对既定抗菌剂(包括氟喹诺酮类)耐药的目标病原体具有体外活性。进行这项研究是为了确定各种尿液参数对gepotidacin和一种比较剂左氧氟沙星对多种细菌的体外活性的影响。

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