Discovery and Optimization of First-in-Class Furopyrimidine-Based Inhibitors of Henipaviruses

Henipaviruses such as Nipah (NiV) and Hendra (HeV) are zoonotic pathogens that cause severe and often fatal respiratory illness and encephalitis in both animals and humans. These viruses exhibit high transmissibility and pandemic potential, a situation made worse by the absence of appropriate pharmaceutical countermeasures. To address this deficit, we conducted a hit-to-lead optimization campaign based on hit <b>1</b> identified through high-throughput screening against recombinant Cedar virus (rCedV), a nonpathogenic surrogate for NiV and HeV. This effort yielded a focused library of analogs that were initially screened against rCedV, with promising candidates subsequently validated against authentic NiV and HeV. Among these, analog <b>46</b> demonstrated superior <i>in vitro</i> metabolic stability and pharmacokinetic properties relative to hit <b>1</b> and is now positioned for <i>in vivo</i> efficacy evaluation. Concurrently, the mechanism of action of these first-in-class furopyrimidine-based antiviral agents was probed through time-of-addition assays, escape mutation analysis, and preliminary <i>in silico</i> modeling.

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Publication Details

Journal
Journal of Medicinal Chemistry
Published
2026-01-06
DOI
https://doi.org/10.1021/acs.jmedchem.5c02646
Primary Topic
Virology and Viral Diseases
Type
article
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article

Discovery and Optimization of First-in-Class Furopyrimidine-Based Inhibitors of Henipaviruses

Christopher C. Broder, Dejan Nikolić, Malaika D. Argade, Sean P. Bradley et al.
Journal of Medicinal Chemistry
Virology and Viral Diseases
article

Discovery and Optimization of First-in-Class Furopyrimidine-Based Inhibitors of Henipaviruses

Christopher C. Broder, Dejan Nikolić, Malaika D. Argade, Sean P. Bradley, Mario Moisés Álvarez, Norton P. Peet, Manu Anantpadma, Ryan Bott, Moushimi Amaya, Robert W. Cross, Terry W. Moore, Paul R. Carlier, Viktoriya Borisevich, Rachel Sarah O’Toole, Łukasz Tomorowicz, Jazmin Galván Achi, Irina N. Gaisina, Arsen Gaisin, Christian A. Zielinski, Lijun Rong, Thomas W. Geisbert
article en

Abstract

Henipaviruses such as Nipah (NiV) and Hendra (HeV) are zoonotic pathogens that cause severe and often fatal respiratory illness and encephalitis in both animals and humans. These viruses exhibit high transmissibility and pandemic potential, a situation made worse by the absence of appropriate pharmaceutical countermeasures. To address this deficit, we conducted a hit-to-lead optimization campaign based on hit <b>1</b> identified through high-throughput screening against recombinant Cedar virus (rCedV), a nonpathogenic surrogate for NiV and HeV. This effort yielded a focused library of analogs that were initially screened against rCedV, with promising candidates subsequently validated against authentic NiV and HeV. Among these, analog <b>46</b> demonstrated superior <i>in vitro</i> metabolic stability and pharmacokinetic properties relative to hit <b>1</b> and is now positioned for <i>in vivo</i> efficacy evaluation. Concurrently, the mechanism of action of these first-in-class furopyrimidine-based antiviral agents was probed through time-of-addition assays, escape mutation analysis, and preliminary <i>in silico</i> modeling.

Journal of Medicinal ChemistryVol. 69(2)
Unifor (NO), University of Illinois Chicago (US), Integrated Oncology (United States) (US), National Institute of Allergy and Infectious Diseases (US), Emergent BioSolutions (Canada) (CA), Drug Discovery Laboratory (Norway) (NO), The University of Texas Medical Branch at Galveston (US)
Good health and well-being
Openalex Percentile: Top 97%
Virology and Viral Diseases
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