首页> 外文期刊>Journal of enzyme inhibition and medicinal chemistry. >The slow dissociation rate of K-1602 contributes to the enhanced inhibitory activity of this novel alkyl-aryl-bearing fluoroketolide
【24h】

The slow dissociation rate of K-1602 contributes to the enhanced inhibitory activity of this novel alkyl-aryl-bearing fluoroketolide

机译:K-1602的缓慢解离速率有助于提高这种新型的含烷基芳基的氟代酮化物的抑制活性

获取原文
获取原文并翻译 | 示例
           

摘要

Ketolides belong to the latest generation of macrolides and are not only effective against macrolide susceptible bacterial strains but also against some macrolide resistant strains. Here we present data providing insights into the mechanism of action of K-1602, a novel alkyl-aryl-bearing fluoroketolide. According to our data, the K-1602 interacts with the ribosome as a one-step slow binding inhibitor, displaying an association rate constant equal to 0.28 x 10(4) M-1 s(-1) and a dissociation rate constant equal to 0.0025 min(-1). Both constants contribute to produce an overall inhibition constant K-i equal to 1.49 x 10(-8) M, which correlates very well with the superior activity of this compound when compared with many other ketolides or fluoroketolides.
机译:酮内酯属于最新一代的大环内酯,不仅对易受大环内酯影响的细菌菌株有效,而且对某些对大环内酯具有抗性的菌株也有效。在这里,我们提供的数据提供了对K-1602(一种新型的含烷基-芳基的氟代酮化物)的作用机理的见解。根据我们的数据,K-1602作为一步一步缓慢结合抑制剂与核糖体相互作用,显示出的缔合速率常数等于0.28 x 10(4)M-1 s(-1),解离速率常数等于0.0025分钟(-1)。这两个常数均有助于产生等于1.49 x 10(-8)M的总抑制常数K-i,与许多其他缩酮或氟代缩酮相比,该常数与该化合物的优越活性非常相关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

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