Evidence map›Paper›PMID 37578235›Full record

ArticleJournal of virology2023

A low-background, fluorescent assay to evaluate inhibitors of diverse viral proteases.

Rebecca A Leonard, Vishwas N Rao, Alexandria Bartlett, Heather M Froggatt, Micah A Luftig, Brook E Heaton, Nicholas S Heaton

Open access · greenAbstract read
In one paragraph

Article in Journal of virology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 30% of its field
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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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

7 authors at 1 institution in 1 country.

Rebecca A LeonardDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine , Durham, North Carolina, USA.ORCID 0000-0002-3404-0399
Vishwas N RaoDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine , Durham, North Carolina, USA.
Alexandria BartlettDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine , Durham, North Carolina, USA.
Heather M FroggattDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine , Durham, North Carolina, USA.
Micah A LuftigDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine , Durham, North Carolina, USA.
Brook E HeatonDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine , Durham, North Carolina, USA.
Nicholas S HeatonDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine , Durham, North Carolina, USA.ORCID 0000-0002-5307-3428
Duke University · US

Funding

Research Project 1: Coronavirus antiviral lead development and combination testingU19AI171292 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SHEAHAN, TIMOTHY PATRICK · 2022 to 2022
$65.5M
Viral Oncology Training GrantT32CA009111 · NCI · DUKE UNIVERSITY · PI LUFTIG, MICAH A. · 1985 to 2023
$8.9M
Medical Scientist Training Program Training GrantT32GM145449 · NIGMS · DUKE UNIVERSITY · PI Christopher D Kontos · 2022 to 2026
$6.6M
NCI NIH HHS T32 CA009111NIAID NIH HHS U19 AI171292NIGMS NIH HHS T32 GM145449
6 · The paper itself

Abstract

Multiple coronaviruses (CoVs) can cause respiratory diseases in humans. While prophylactic vaccines designed to prevent infection are available for severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), incomplete vaccine efficacy, vaccine hesitancy, and the threat of other pathogenic CoVs for which vaccines do not exist have highlighted the need for effective antiviral therapies. While antiviral compounds targeting the viral polymerase and protease are already in clinical use, their sensitivity to potential resistance mutations as well as their breadth against the full range of human and preemergent CoVs remain incompletely defined. To begin to fill that gap in knowledge, we report here the development of an improved, noninfectious, cell-based fluorescent assay with high sensitivity and low background that reports on the activity of viral proteases, which are key drug targets. We demonstrate that the assay is compatible with not only the SARS-CoV-2 M

Indexed as

Antiviral AgentsProtease InhibitorsViral ProteasesCoronavirus 3C ProteasesCOVID-19HumansIndazolesLactamsLeucineNitrilesProlineSARS-CoV-2TriazinesTriazoles3C-like proteinase, SARS-CoV-2Antiviral AgentsCoronavirus 3C ProteasesensitrelvirIndazolesLactamsLeucinenirmatrelvirNitrilesProlineProtease InhibitorsTriazinesTriazolesViral ProteasesantiviralscoronavirusesCoV MproCoV PLproEpstein–Barr virusFlipGFPZika virus

Identifiers

PMID37578235
PMCPMC10506478
OpenAlexW4385797854

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 Socratic graph.