فهرست نشریات علمی دسترسی آزاد ایران

Emerging and re-emerging RNA viruses continue to pose global health threats, highlighting the need for broad-spectrum antivirals that can be rapidly deployed against diverse viral families. Molnupiravir, a nucleoside analog that induces lethal mutagenesis, has shown promise as a broad-spectrum antiviral; yet, its efficacy across virus families remains incompletely mapped. This study systematically profiles the published antiviral activity of molnupiravir across all available virus families, genome types, and experimental systems, aiming to clarify determinants of susceptibility and to identify critical data gaps. A meta-analytic extraction and harmonization of all published EC50/IC50 values were performed, including assay metadata and comparator drugs where available. Statistical analyses and hierarchical clustering were used to visualize potency, breadth, and functional groupings across the viral landscape. The dataset comprises over 60 unique data points covering 13 virus families, with the most robust evidence for Coronaviridae, Orthomyxoviridae, and Togaviridae. Respiratory viruses, including SARS-CoV-2, influenza, and RSV, showed exceptional sensitivity (median EC50<1 μM), while some flaviviruses and filoviruses were less susceptible. Potency was strongly influenced by both viral genome type and experimental system, with cell type and assay selection producing up to 10-fold variation in reported EC50. Head-to-head analysis demonstrated superior or equivalent potency of molnupiravir compared to remdesivir, favipiravir, and ribavirin across key viral families. Hierarchical clustering revealed that mechanistic susceptibility often transcends strict taxonomic boundaries, suggesting conserved determinants of drug action. Critical research gaps persist for several important families, including Bunyavirales and Arenaviridae. This comprehensive mapping provides a foundational resource for pandemic preparedness, rational antiviral stockpiling, and future drug development targeting broad viral threats.