Evidence map›Paper›PMID 41931700›Full record

ArticleACS infectious diseases2026

SARS-CoV-2 Antivirals Identified from Small Molecule Modulators of Programmed -1 Ribosomal Frameshifting.

Emily G Swanson Hay, Madison M Maille, Martina Zafferani, Maritza Puray-Chavez, Ming Xia, TinTin B Luu, Dhanasheel Muralidharan, Mei-Ling Li, Gary Brewer, Sebla B Kutluay and 2 more

Abstract read
In one paragraph

Article in ACS infectious diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Emily G Swanson HayDepartment of Chemistry, Duke University, 124 Science Drive, Durham, North Carolina 27708, United States.
Madison M MailleDepartment of Chemistry and Biochemistry, Loyola Marymount University, Los Angeles, California 90045, United States.
Martina ZafferaniDepartment of Chemistry, Duke University, 124 Science Drive, Durham, North Carolina 27708, United States.
Maritza Puray-ChavezDepartment of Molecular Microbiology, Washington University School of Medicine, Saint Louis, Missouri 63110, United States.
Ming XiaDepartment of Molecular Microbiology, Washington University School of Medicine, Saint Louis, Missouri 63110, United States.
TinTin B LuuDepartment of Chemistry, University of Toronto, Mississauga, Ontario L5L 1C6, Canada.
Dhanasheel MuralidharanDepartment of Chemistry, Duke University, 124 Science Drive, Durham, North Carolina 27708, United States.
Mei-Ling LiDepartment of Biochemistry and Molecular Biology, Rutgers Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, United States.
Gary BrewerDepartment of Biochemistry and Molecular Biology, Rutgers Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, United States.
Sebla B KutluayDepartment of Molecular Microbiology, Washington University School of Medicine, Saint Louis, Missouri 63110, United States.
Kathryn D MouzakisDepartment of Chemistry and Biochemistry, Loyola Marymount University, Los Angeles, California 90045, United States.ORCID 0000-0001-6355-8851
Amanda E HargroveDepartment of Chemistry, University of Toronto, Mississauga, Ontario L5L 1C6, Canada.ORCID 0000-0003-1536-6753

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Remaining SARS-CoV-2 vulnerable populations and the threat of viral resistance to existing immunity and COVID-19 vaccines highlight the need to expand treatment options. While the number of SARS-CoV-2 viral proteins is limited for therapeutic targeting, the RNA genome offers a wide range of conserved functional structures. Previous studies suggest that modulating the RNA-regulated programmed -1 ribosomal frameshift (-1 PRF) step in the coronavirus life cycle can inhibit viral replication. In this work, we aimed to identify small molecules that target the highly conserved SARS-CoV-2 frameshift site pseudoknot. An RNA-biased synthetic small molecule library screen against the RNA pseudoknot structure identified several candidate molecules. Of these, seven showed evidence of dose-dependent activity in in vitro and in cellulo frameshift assays and inhibited SARS-CoV-2 replication in cell culture. While binding was required for activity, affinity did not correlate with frameshift inhibition. Similarly, small molecule impacts to pseudoknot stability, as measured with an RT-qPCR assay, did not predict impacts on the frameshift efficiency. Comparison of the hits, as well as previously published inhibitors, across several assays supports the need for multiple characterization methods in small molecule-RNA targeting and the possibility of multiple modes of action for -1 PRF modulation. This work underscores the complexity of targeting dynamic RNA structures and the benefits of screening early for function and later optimizing for mode of action. The use of orthogonal techniques led to the identification of several promising hits and a lead antiviral compound.

Indexed as

Antiviral AgentsBetacoronavirusFrameshifting, RibosomalRNA, ViralSARS-CoV-2Small Molecule LibrariesAnimalsChlorocebus aethiopsCOVID-19 Drug TreatmentHumansNucleic Acid ConformationRNA ReplicationVirus ReplicationAntiviral AgentsRNA, ViralSmall Molecule LibrariesantiviralsframeshiftingpseudoknotRNASARS-CoV-2small molecules

Identifiers

PMID41931700
PMCPMC13162254

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.