Abstract
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.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
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Review
MeSH terms
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Animals
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Anti-Bacterial Agents* / chemical synthesis
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Anti-Bacterial Agents* / chemistry
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Anti-Bacterial Agents* / pharmacology
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Anti-Bacterial Agents* / therapeutic use
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Bacterial Infections / drug therapy*
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Bacterial Infections / microbiology
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Communicable Diseases, Emerging / drug therapy*
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Communicable Diseases, Emerging / microbiology
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Drug Design
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Drug Discovery*
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Drug Resistance, Bacterial
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Drug Resistance, Multiple, Bacterial
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Gram-Negative Bacteria / drug effects
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Humans
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Methicillin-Resistant Staphylococcus aureus / drug effects
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Microbial Sensitivity Tests
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Mycobacterium tuberculosis / drug effects
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Small Molecule Libraries
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Staphylococcus aureus / drug effects
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Technology, Pharmaceutical*
Substances
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Anti-Bacterial Agents
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Small Molecule Libraries