Introduction Of A Thio Functional Group To Diazabicyclooctane: An Effective Modification To Potentiate The Activity Of Beta-Lactams Against Gram-Negative Bacteria Producing Class A, C, And D Serine Beta-Lactamases
ACS INFECTIOUS DISEASES(2020)
摘要
By the emergence and worldwide spread of multi-drug-resistant Gram-negative bacteria, there have been growing demands for efficacious drugs to cure these resistant infections. The key mechanism for resistance to beta-lactam antibiotics is the production of beta-lactamases, which hydrolyze and deactivate beta-lactams. Diazabicyclooctane (DBO) analogs play an important role as one of the new classes of beta-lactamase inhibitors (BLIs), and several compounds such as avibactam (AVI) have been approved by the FDA, along with many derivatives under clinical or preclinical development. Although these compounds have a similar amide substituent at the C2 position, we have recently reported the synthesis of novel DBO analogs which possess a thio functional group. This structural modification enhances the ability to restore the antimicrobial activities of cefixime (CMF) against pathogens producing classes A, C, and D serine beta-lactamases compared with AVI and expands the structural tolerance at the six position. Furthermore, some of these analogs showed intrinsic microbial activities based on multipenicillin binding protein (PBP) inhibition. This is the unique feature which has never been observed in DBOs. One of our DBOs had a pharmacokinetic profile comparable to that of other DBOs. These results indicate that the introduction of a thio functional group into DBO is a novel and effective modification to discover a clinically useful new BLI.
更多查看译文
关键词
beta-lactamase inhibitor, BLI, diazabicyclooctane, DBO, CRE, ESBL
AI 理解论文
溯源树
样例
![](https://originalfileserver.aminer.cn/sys/aminer/pubs/mrt_preview.jpeg)
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要