Perspective highlights pleuromutilin derivatives' enhanced antibacterial activity against resistant bacteria, suggesting innovative drug development.
Pleuromutilin is a natural product with promising therapeutic potential and important applications for antimicrobial drug development. The semisynthetic pleuromutilin derivatives obtained through structural modification of the C-14 side chain exhibit significantly enhanced antibacterial activity and pharmacokinetic properties. These compounds specifically bind to the peptidyl transferase center of the bacterial 50S ribosomal subunit to inhibit protein synthesis. To date, pleuromutilin derivatives have shown efficacy against drug-resistant Gram-positive bacteria, some Gram-negative bacteria, and Mycoplasma. This Perspective systematically summarizes research advances in the structural modification and antibacterial activity of pleuromutilin derivatives, with a focus on breakthrough achievements in enhancing antibacterial potency through innovative side-chain designs from 2015 to 2025. Furthermore, this study highlights future directions for innovative drug development based on pleuromutilin structural modification, offering insights into addressing the global challenge of antibiotic resistance.
No takes yet. Share an insight, caveat, or question.
Liu et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: