Year: 2026
Type: article
Abstract: Antimicrobial resistance (AMR) is a worsening global health crisis, with drug repurposing emerging as a key mitigation strategy. Pyrimidine nucleosides are promising antibacterial scaffolds due to their easily modifiable structures and multi-therapeutic potential. However, related research faces challenges, including fragmented structure-activity relationships (SAR), unclear metabolism-efficacy correlations, and limited clinical translation strategies. This review categorizes these derivatives into cytosine and uracil/thymine analogs. It analyzes how lipidation, selenylation, and other structural modifications regulate antibacterial activity by modulating target binding, membrane permeability, and metabolic stability. Crucially, it elucidates their metabolic activation mechanism. As prodrugs, these derivatives require intracellular enzymatic phosphorylation to form active metabolites that inhibit nucleic acid synthesis, and their efficacy is dependent on intracellular enzyme levels and activity. Additionally, the review identifies core clinical translation barriers (host toxicity, narrow spectrum, insufficient AMR research) and proposes targeted optimization strategies (e.g., enzyme-guided modification and combination therapy). By integrating disparate structure-activity relationship and metabolic mechanism research, this work provides a novel systematic framework for developing pyrimidine nucleosides. Furthermore, it offers critical support to address the global antimicrobial resistance (AMR) crisis.
Source: Frontiers in Pharmacology
Authors: Binjie Xu, Pengyu Li, Jiping Liu, Mingkai Li
Language: English
Subfield: Organic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $3,801
OpenAlex ID: W7133844741