A combination strategy of a semisynthetic macrolide, 5-O-mycaminosyltylonolide with polymyxin B nonapeptide for multi-drug resistance P. aeruginosa
Author:
Publisher
Springer Science and Business Media LLC
Subject
Drug Discovery,Pharmacology
Link
https://www.nature.com/articles/s41429-023-00628-9.pdf
Reference13 articles.
1. Antibiotic Resistance Threats in the United States. U.S. Department of Health and Human Services:CDC;2019. Available from: https://www.cdc.gov/drugresistance/Biggest-Threats.html.
2. Murray CJL, et al. Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis. Lancet. 2022;399:629–55.
3. Fischbach MA, Walsh CT, et al. Antibiotics for emerging pathogens. Science. 2009;325:1089–93.
4. Willyard C. The drug-resistant bacteria that pose the greatest health threats. Nature. 2017;543:15.
5. Payne DJ, Gwynn MN, Holmes DJ, Pompliano DL. Drugs for bad bugs: confronting the challenges of antibacterial discovery. Nat Rev Drug Disco. 2007;6:29–40.
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Efflux pump inhibitor, phenylalanine-arginine beta-naphthylamide analog potentiates the activity of 5-O-mycaminosyltylonolide for multi-drug resistant Pseudomonas aeruginosa;The Journal of Antibiotics;2024-03-11
2. Overcoming Native Macrolide and Acquired Multidrug-Resistant <i>Pseudomonas aeruginosa</i> with Azithromycin and Polymyxin B Nonapeptide;BPB Reports;2023
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