首页> 美国卫生研究院文献>Antimicrobial Agents and Chemotherapy >Comparative In Vitro Activities of AC98-6446 a Novel Semisynthetic Glycopeptide Derivative of the Natural Product Mannopeptimycin α and Other Antimicrobial Agents against Gram-Positive Clinical Isolates
【2h】

Comparative In Vitro Activities of AC98-6446 a Novel Semisynthetic Glycopeptide Derivative of the Natural Product Mannopeptimycin α and Other Antimicrobial Agents against Gram-Positive Clinical Isolates

机译:天然产物甘露肽霉素α的新型半合成糖肽衍生物AC98-6446和其他抗革兰氏阳性临床隔离药物的体外比较活性

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

AC98-6446 is a novel semisynthetic cyclic glycopeptide antibiotic related to the natural product mannopeptimycin α (AC98-1). In the present study the activity of AC98-6446 was evaluated against a variety of recent clinical gram-positive pathogens including multiply resistant strains. AC98-6446 demonstrated similar potent activities against methicillin-susceptible and methicillin-resistant staphylococci and glycopeptide-intermediate staphylococcal isolates (MICs at which 90% of isolates are inhibited [MIC90s], 0.03 to 0.06 μg/ml). AC98-6446 also demonstrated good activities against both vancomycin-resistant and -susceptible strains of enterococci (MIC90s, 0.12 and 0.25 μg/ml, respectively) as well as against streptococcal strains (MIC90s, ≤ 0.008 to 0.03 μg/ml). AC98-6446 demonstrated bactericidal activity in terms of the reduction in the viable counts (>3 log10 CFU/ml) of staphylococcal and streptococcal isolates and a marked decrease in the viable counts of most enterococcal strains (from 0.2 to 2.5 log10 CFU/ml). Unlike vancomycin, which demonstrates time-dependent killing, AC98-6446 demonstrated concentration-dependent killing. The potent activity, novel structure, and bactericidal activity demonstrated by AC98-6446 make it an attractive candidate for further development.
机译:AC98-6446是一种新型的半合成环状糖肽抗生素,与天然产物甘露肽霉素α(AC98-1)有关。在本研究中,评估了AC98-6446对多种近期临床革兰氏阳性病原体(包括多重耐药菌株)的活性。 AC98-6446对甲氧西林易感和耐甲氧西林的葡萄球菌和糖肽中间的葡萄球菌分离株(抑制90%分离株的MICs [MIC90s],0.03至0.06μg/ ml)表现出相似的有效活性。 AC98-6446还显示出抗万古霉素和敏感肠球菌菌株(分别为MIC90s,0.12和0.25μg/ ml)以及链球菌菌株(MIC90s,≤0.008至0.03μg/ ml)的良好活性。 AC98-6446表现出杀菌活性,表明葡萄球菌和链球菌分离株的活菌数减少(> 3 log10 CFU / ml),大多数肠球菌菌株的活菌数显着下降(从0.2到2.5 log10 CFU / ml) 。与显示时间依赖性杀伤的万古霉素不同,AC98-6446显示浓度依赖性杀伤。 AC98-6446证明的有效活性,新颖的结构和杀菌活性使其成为进一步开发的有吸引力的候选对象。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号