Exploration of 4′-fluoro fleximer nucleoside analogues as potential broad-spectrum antiviral agents.

Publication date: Oct 01, 2025

A series of 4′-fluoro fleximer nucleoside analogues in addition to their corresponding prodrugs were designed, synthesized, and evaluated for their antiviral potential. The impetus for this series was based on the success of other 4′-modified nucleoside antiviral drugs such as adafosbuvir and balapiravir. One analogue, KAD-008, exhibited potent, low single-digit micromolar activity against DENV-2. Another analogue, KAD-025, had broad-spectrum antiviral activity across several viral families including flaviviruses, filoviruses, and coronaviruses. All of the analogues tested showed no toxicity up to 100 uM. Additional studies are underway to elucidate the mechanism of action for these compounds and to synthesize additional 4′-modified fleximer nucleoside analogues with different 4′-modifications to compare their antiviral activities.

Concepts Keywords
100m Animals
Bioorg Antiviral
Flaviviruses Antiviral Agents
Fluoro Antiviral Agents
Low Dengue
Dengue Virus
Dose-Response Relationship, Drug
Flavivirus
Fleximers
Humans
Microbial Sensitivity Tests
Molecular Structure
Nucleosides
Nucleosides
Nucleosides
Prodrugs
Structure-Activity Relationship

Semantics

Type Source Name
drug DRUGBANK Spinosad
drug DRUGBANK Balapiravir
disease MESH Dengue

Original Article

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