Identification of Spirodioxolane nsP2 Helicase Inhibitors with Antialphaviral Activity

We describe the design, synthesis, and antialphaviral activity of spirodioxolane inhibitors targeting the alphavirus nsP2 helicase (nsP2hel). The spirodioxolanes are a new series of direct-acting antivirals that retain key molecular features required for inhibition of nsP2hel, including a highly substituted piperidine acetamide with its associated conformational isomerism and thermal mobility. Unlike the related oxaspiropiperidine nsP2hel inhibitors, the spirodioxolanes showed no enantioselectivity in their antiviral activity. The spirodioxolanes demonstrated antialphaviral activity against the Old World alphavirus Chikungunya virus, with some analogs also showing activity against the New World alphavirus Venezuelan equine encephalitis virus. Importantly, certain spirodioxolane analogs, such as 6b, maintained activity against viral mutants that displayed resistance to first-generation oxaspiropiperidine inhibitors, indicating their potential for optimization as a new class of broad-spectrum antialphaviral drugs.

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Journal
ChemRxiv
Published
2025-09-01
DOI
https://doi.org/10.26434/chemrxiv-2025-mfts7
Primary Topic
Hepatitis Viruses Studies and Epidemiology
Type
article
Field-Weighted Citation Impact
0.00

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article

Identification of Spirodioxolane nsP2 Helicase Inhibitors with Antialphaviral Activity

Rahman Shah Zaib Saleem, John D. Sears, Mark T. Heise, Hans Y. Oh et al.
ChemRxiv
Hepatitis Viruses Studies and Epidemiology
article

Identification of Spirodioxolane nsP2 Helicase Inhibitors with Antialphaviral Activity

Rahman Shah Zaib Saleem, John D. Sears, Mark T. Heise, Hans Y. Oh, Zachary W. Davis‐Gilbert, Sabian A. Martinez, Nathaniel J. Moorman, Rafael M. Couñago, Durbadal Ojha, Matthew H. Todd, Timothy M. Willson, Mohammad Anwar Hossain, Jane Burdick, M. Bose, Stella R. Moorman
article en

Abstract

We describe the design, synthesis, and antialphaviral activity of spirodioxolane inhibitors targeting the alphavirus nsP2 helicase (nsP2hel). The spirodioxolanes are a new series of direct-acting antivirals that retain key molecular features required for inhibition of nsP2hel, including a highly substituted piperidine acetamide with its associated conformational isomerism and thermal mobility. Unlike the related oxaspiropiperidine nsP2hel inhibitors, the spirodioxolanes showed no enantioselectivity in their antiviral activity. The spirodioxolanes demonstrated antialphaviral activity against the Old World alphavirus Chikungunya virus, with some analogs also showing activity against the New World alphavirus Venezuelan equine encephalitis virus. Importantly, certain spirodioxolane analogs, such as 6b, maintained activity against viral mutants that displayed resistance to first-generation oxaspiropiperidine inhibitors, indicating their potential for optimization as a new class of broad-spectrum antialphaviral drugs.

ChemRxiv
University of North Carolina at Chapel Hill (US), University College London (GB)
National Institutes of Health
Openalex Percentile: Top 68%
Hepatitis Viruses Studies and Epidemiology
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