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首页> 外文期刊>Antimicrobial agents and chemotherapy. >Activity of a Novel 1,3-Beta-D-Glucan Synthase Inhibitor, Ibrexafungerp (Formerly SCY-078), against Candida glabrata
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Activity of a Novel 1,3-Beta-D-Glucan Synthase Inhibitor, Ibrexafungerp (Formerly SCY-078), against Candida glabrata

机译:新的1,3-Beta-d-glucan合酶抑制剂,Ibrexafungerp(以前Scy-078)的活性,针对念珠菌葡萄球菌

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摘要

Ibrexafungerp (formerly SCY-078), a novel glucan synthase inhibitor with oral availability, was evaluated for activity against Candida glabrata. The susceptibility of clinical strains to ibrexafungerp was determined by microdilution and time-kill assays. The MIC range against wild-type strains was 1 to 2 mu g/ml. Ibrexafungerp was also active against the majority of echinocandin-resistant strains. Time-kill studies showed 4- to 6-log-unit reductions in growth at 24 and 48 h with concentrations of 0.25 to 4 mu g/ml.
机译:Ibrexafungerp(前身SCY-078)是一种具有口服可用性的新型葡聚糖合成酶抑制剂,用于针对念珠菌Glabrata的活性。 通过微稀释和时间杀死测定法测定临床菌株对伊布拉菲吞噬器的敏感性。 对野生型菌株的麦克风范围为1至2μg/ ml。 Ibraxafungerp也针对大多数棘突抗性菌株活跃。 时间杀死研究表明,在24和48小时的浓度为0.25至4μg/ ml时表现出4-6次逻辑单元的生长减少。

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