抗生素
重新调整用途
抗生素耐药性
生物
致病菌
药物发现
多重耐药
细菌
计算生物学
微生物学
生物信息学
遗传学
生态学
作者
Michael A. Fischbach,Christopher T. Walsh
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2009-08-28
卷期号:325 (5944): 1089-1093
被引量:1542
标识
DOI:10.1126/science.1176667
摘要
Antibiotic-resistant strains of pathogenic bacteria are increasingly prevalent in hospitals and the community. New antibiotics are needed to combat these bacterial pathogens, but progress in developing them has been slow. Historically, most antibiotics have come from a small set of molecular scaffolds whose functional lifetimes have been extended by generations of synthetic tailoring. The emergence of multidrug resistance among the latest generation of pathogens suggests that the discovery of new scaffolds should be a priority. Promising approaches to scaffold discovery are emerging; they include mining underexplored microbial niches for natural products, designing screens that avoid rediscovering old scaffolds, and repurposing libraries of synthetic molecules for use as antibiotics.
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