Evidence map›Paper›PMID 42067193›Full record

ArticleSLAS discovery : advancing life sciences R & D2026

Repurposing drug screen for the identification of helicase inhibitors from viruses of pandemic concern.

Nicole L Inniss, Margarita Rzhetskaya, Ryan P Kich, Elizabeth Gleason, Taha Y Taha, Francisco J Zapatero-Belinchón, Julia Rosecrans, Valentina Pedrero-Classen, Kenneth Huang, Gilles Degotte and 8 more

Abstract read
In one paragraph

Article in SLAS discovery : advancing life sciences R & D, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

18 authors.

Nicole L InnissDepartment of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Center for Structural Biology of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Margarita RzhetskayaDepartment of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Center for Pathogen Genomics and Microbial Evolution, Havey Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Ryan P KichDepartment of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Elizabeth GleasonDepartment of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Center for Structural Biology of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Taha Y TahaDepartment of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, CA, USA; Gladstone Infectious Disease Institute, Gladstone Institutes, San Francisco, CA, USA.
Francisco J Zapatero-BelinchónGladstone Infectious Disease Institute, Gladstone Institutes, San Francisco, CA, USA.
Julia RosecransGladstone Infectious Disease Institute, Gladstone Institutes, San Francisco, CA, USA.
Valentina Pedrero-ClassenGladstone Infectious Disease Institute, Gladstone Institutes, San Francisco, CA, USA.
Kenneth HuangDepartment of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, CA, USA.
Gilles DegotteDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA, USA.
Luca LizzadroDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA, USA.
Jason PattieDepartment of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Center for Structural Biology of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Adam R RensloDepartment of Pharmaceutical Chemistry, University of California, San Francisco, San Francisco, CA, USA.
George MinasovDepartment of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Center for Structural Biology of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Melanie OttDepartment of Bioengineering and Therapeutic Sciences, University of California San Francisco, San Francisco, CA, USA; Gladstone Infectious Disease Institute, Gladstone Institutes, San Francisco, CA, USA; Department of Medicine, University of California at San Francisco, San Francisco, CA, USA; Chan Zuckerberg Biohub - San Francisco, San Francisco, CA, USA.
Kelly E R BachtaDepartment of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Center for Pathogen Genomics and Microbial Evolution, Havey Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, USA.
Karla J F SatchellDepartment of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Center for Structural Biology of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Center for Pathogen Genomics and Microbial Evolution, Havey Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. Electronic address: k-satchell@northwestern.edu.
Judd F HultquistDepartment of Microbiology-Immunology, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Department of Medicine, Division of Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, IL, USA; Center for Pathogen Genomics and Microbial Evolution, Havey Institute for Global Health, Northwestern University Feinberg School of Medicine, Chicago, IL, USA. Electronic address: judd.hultquist@northwestern.edu.

Funding

Targeting Viroporins and Coronavirus M ProteinU19AI171110 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI James Solomon Fraser · 2022 to 2026
$103.4M
TO PROVIDE SCIENTIFIC SUPPORT TO THE CENTERS FOR RESEARCH ON STRUCTURAL BIOLOGY OF INFECTIOUS DISEASES.75N93022C00035 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI SATCHELL, KARLA · 2022 to 2025
$20.7M
Viral and Host Dynamics during Pediatric COVID-19 and Respiratory Virus Co-InfectionR01AI177498 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Bria M Coates, Judd F Hultquist · 2024 to 2026
$2.4M
NIAID NIH HHS R01 AI177498NIAID NIH HHS U19 AI171110NIH HHS 75N93022C00035
6 · The paper itself

Abstract

Several families of viruses encode helicase enzymes with essential roles in viral genome replication and transcription, including several RNA virus families of pandemic concern, such as coronaviruses and flaviviruses. Viral helicases are widely considered to be promising antiviral targets with some DNA virus helicase inhibitors already approved for clinical use. Here, we demonstrate that the SARS-CoV-2 viral helicase, nsp13, is essential for viral replication. Using a previously developed in vitro helicase dsRNA unwinding assay, we screened 208 repurposed small molecules for nsp13 inhibition. Nine of these small molecules had a half-maximal inhibitory concentration (IC

Indexed as

Antiviral AgentsDrug RepositioningEnzyme InhibitorsRNA HelicasesSARS-CoV-2Viral Nonstructural ProteinsAnimalsCOVID-19 Drug TreatmentDrug Evaluation, PreclinicalHumansMethyltransferasesMolecular Docking SimulationPandemicsVirus ReplicationYellow fever virusAntiviral AgentsEnzyme InhibitorsMethyltransferasesNsp13 protein, SARS-CoVRNA HelicasesViral Nonstructural ProteinsAntiviral drug discoveryDrug repurposingHelicaseNS3nsp13SARS-CoV-2YFV

Identifiers

PMID42067193
PMCPMC13387393

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.