...
首页> 外文期刊>Chemical biology and drug design >4‐Substituted thieno[2,3‐ dd ]pyrimidines as potent antibacterial agents: Rational design, microwave‐assisted synthesis, biological evaluation and molecular docking studies
【24h】

4‐Substituted thieno[2,3‐ dd ]pyrimidines as potent antibacterial agents: Rational design, microwave‐assisted synthesis, biological evaluation and molecular docking studies

机译:4-取代的噻吩[2,3- D]嘧啶作为有效的抗菌剂:合理设计,微波辅助合成,生物学评估和分子对接研究

获取原文
获取原文并翻译 | 示例
           

摘要

> In an attempt to discover a new class of antibacterial agents with improved efficacy and to overcome the drug‐resistant problems, some novel 4‐substituted thieno[2,3‐ d ]pyrimidines have been synthesized via microwave‐assisted methodology and evaluated for their in vitro antibacterial activity against various pathogenic bacterial strains. Compounds 12 b and 13 c showed the promising inhibitory potencies against Staphylococcus aureus , Bacillus subtilis , Pseudomonas aeruginosa and Escherichia coli with MIC s ranging from 2 to 10?μg/ml. Compound 13 c was also found to be highly potent against methicillin‐resistant S. aureus ( MRSA ) with MIC value of 4?μg/ml. Docking simulation studies have been performed to unravel the mode of action and association study indicate the binding of potent compounds with DHPS enzyme. In silico ADME studies suggest the drug‐like characteristics of the potent compounds.
机译:

试图发现一类新的抗菌剂,具有改善的疗效和克服耐药性问题,一些新的4替代通过微波辅助方法合成噻吩并通过微波辅助方法合成嘧啶,并针对各种致病细菌菌株评估其体外抗菌活性。化合物 12 <Ⅰ> B /Ⅰ>和 13 / b> c 显示具有抑制抑制性疗效,含有金黄色葡萄球菌,枯草芽孢杆菌,枯草芽孢杆菌,假单胞菌铜绿假单胞菌和大肠杆菌,与 MIC S的范围为2至10?μg/ ml。还发现复合 13 / B> C 对耐甲氧脲的抗性感到高效。 AUREUS MRSA ),具有 MIC 值4≤μg/ mL。已经进行了对接模拟研究以解开作用和关联研究表明有效化合物与 DHPS 酶的结合。在Silico Adme 研究表明有效化合物的药物状特征。

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