Evidence map›Paper›PMID 38126789›Full record

ArticlemBio2024

Potent 3CLpro inhibitors effective against SARS-CoV-2 and MERS-CoV in animal models by therapeutic treatment.

Pengfei Li, Yunjeong Kim, Chamandi S Dampalla, Harry Nhat Nguyen, David K Meyerholz, David K Johnson, Scott Lovell, William C Groutas, Stanley Perlman, Kyeong-Ok Chang

Abstract read
In one paragraph

Article in mBio, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

10 authors.

Pengfei LiDepartment of Microbiology and Immunology, The University of Iowa, lowa, USA.
Yunjeong KimDepartment of Diagnostic Medicine and Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA.ORCID 0000-0002-2977-4400
Chamandi S DampallaDepartment of Chemistry, Wichita State University, Wichita, Kansas, USA.
Harry Nhat NguyenDepartment of Chemistry, Wichita State University, Wichita, Kansas, USA.
David K MeyerholzDepartment of Pathology, The University of Iowa, Iowa, USA.
David K JohnsonComputational Chemical Biology Core, The University of Kansas, Lawrence, Kansas, USA.
Scott LovellProtein Structure Laboratory, The University of Kansas, Lawrence, Kansas, USA.
William C GroutasDepartment of Chemistry, Wichita State University, Wichita, Kansas, USA.ORCID 0000-0001-5248-7912
Stanley PerlmanDepartment of Microbiology and Immunology, The University of Iowa, lowa, USA.ORCID 0000-0003-4213-2354
Kyeong-Ok ChangDepartment of Diagnostic Medicine and Pathobiology, College of Veterinary Medicine, Kansas State University, Manhattan, Kansas, USA.ORCID 0000-0002-4435-3751

Funding

Vector Core-Core 2P30DK054759 · NIDDK · UNIVERSITY OF IOWA · PI Alejandro Antonio Pezzulo · 1998 to 2026
$30.5M
SARS-CoV Proteins in Heterologous Viral InfectionP01AI060699 · NIAID · UNIVERSITY OF IOWA · PI PERLMAN, STANLEY · 2004 to 2021
$21.5M
Small Molecule Protease Inhibitors against MERS-CoV and Coronaviruses of Pandemic PotentialR01AI130092 · NIAID · KANSAS STATE UNIVERSITY · PI Kyeong-Ok Chang, William Constantine Groutas · 2018 to 2026
$5.9M
Role of eicosanoids in pathogenic human CoV infectionsR01AI129269 · NIAID · UNIVERSITY OF IOWA · PI Stanley Perlman · 2016 to 2026
$4.7M
Norovirus 3CL Protease-Based Anti-norovirus TherapeuticsR01AI109039 · NIAID · KANSAS STATE UNIVERSITY · PI BOWLIN, TERRY L., CHANG, KYEONG-OK · 2014 to 2018
$3.7M
Small Molecule Inhibitors Against 3C-Like Protease of SARS-CoV-2R01AI161085 · NIAID · KANSAS STATE UNIVERSITY · PI Kyeong-Ok Chang, William Constantine Groutas · 2021 to 2026
$3.7M
NIAID NIH HHS P01 AI060699NIAID NIH HHS R01 AI109039NIAID NIH HHS R01 AI129269NIAID NIH HHS R01 AI130092NIAID NIH HHS R01 AI161085NIDDK NIH HHS P30 DK054759
6 · The paper itself

Abstract

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and Middle East respiratory syndrome coronavirus (MERS-CoV) are zoonotic betacoronaviruses that continue to have a significant impact on public health. Timely development and introduction of vaccines and antivirals against SARS-CoV-2 into the clinic have substantially mitigated the burden of COVID-19. However, a limited or lacking therapeutic arsenal for SARS-CoV-2 and MERS-CoV infections, respectively, calls for an expanded and diversified portfolio of antivirals against these coronavirus infections. In this report, we examined the efficacy of two potent 3CLpro inhibitors,

Indexed as

COVID-19Hepatitis C, ChronicMiddle East Respiratory Syndrome CoronavirusAnimalsAntiviral AgentsDisease Models, AnimalHumansMiceSARS-CoV-2Antiviral Agents3CLproanimal modelsMERS-CoVprotease inhibitorsSARS-CoV-2

Identifiers

PMID38126789
PMCPMC10865860

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.