Evidence map›Paper›PMID 25451075›Full record

ArticleAntiviral research2015

A screen of the NIH Clinical Collection small molecule library identifies potential anti-coronavirus drugs.

Jianzhong Cao, J Craig Forrest, Xuming Zhang

2 registry-linked trialsAbstract read
In one paragraph

Article in Antiviral research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 106 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
106citing papers in PubMed, 1 pooled it
–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.

NCT04459286 phase2terminatednot on this mapstarted 2020, after this paper: background citation

A Randomized, Open Label Trial to Investigate the Efficacy and Safety of Nitazoxanide Plus Atazanavir/Ritonavir for the Treatment of COVID-19: a Pilot Study

TypeinterventionalSponsorObafemi Awolowo UniversityRan2020 to 2021Enrolled57ConditionsCovid-19ArmsNitazoxanide and atazanavir/ritonavir, Standard of Care
NCT04498936 phase4completednot on this mapstarted 2020, after this paper: background citation

Efficacy of Adding Sofosbuvir/Ledipasvir Combination, or Nitazoxanide to the Standard of Care in Treatment of COVID-19: A Randomized Controlled Trial

TypeinterventionalSponsorAssiut UniversityRan2020 to 2020Enrolled240ConditionsCOVIDArmsSofosbuvir and Ledipasvir, Nitazoxanide
3 · Its place in the literature

Who cites it

106 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  7. Reporter-expressing viruses for antiviral drug discovery research.Frontiers in cellular and infection microbiology · 2025
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  14. AnJournal of virology · 2024
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46 more citing papers are in PubMed but not listed here.

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

3 authors.

Jianzhong CaoDepartment of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, United States.
J Craig ForrestDepartment of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, United States.
Xuming ZhangDepartment of Microbiology and Immunology, University of Arkansas for Medical Sciences, Little Rock, AR 72205, United States. Electronic address: zhangxuming@uams.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With the recent emergence of Middle East Respiratory Syndrome coronavirus in humans and the outbreak of devastating porcine epidemic diarrhea coronavirus in swine, therapeutic intervention is urgently needed. However, anti-coronavirus drugs currently are not available. In an effort to assist rapid development of anti-coronavirus drugs, here we screened the NIH Clinical Collection in cell culture using a luciferase reporter-expressing recombinant murine coronavirus. Of the 727 compounds screened, 84 were found to have a significant anti-coronavirus effect. Further experiments revealed that 51 compounds blocked virus entry while 19 others inhibited viral replication. Additional validation studies with the top 3 inhibitors (hexachlorophene, nitazoxanide and homoharringtonine) demonstrated robust anti-coronavirus activities (a reduction of 6 to 8log10 in virus titer) with an IC50 ranging from 11nM to 1.2μM. Furthermore, homoharringtonine and hexachlorophene exhibited broad antiviral activity against diverse species of human and animal coronaviruses. Since the NIH Clinical Collection consists of compounds that have already been through clinical trials, these small molecule inhibitors have a great potential for rapid development as anti-coronavirus drugs.

Indexed as

Drug DiscoverySmall Molecule LibrariesAnimalsAntiviral AgentsCell LineCoronavirusHarringtoninesHexachloropheneHomoharringtonineHumansLuciferasesMiceMurine hepatitis virusNitro CompoundsThiazolesViral LoadAntiviral AgentsHarringtoninesHexachloropheneHomoharringtonineLuciferasesnitazoxanideNitro CompoundsSmall Molecule LibrariesThiazolesCoronavirusNCC libraryScreeningSmall molecule

Identifiers

PMID25451075
PMCPMC7113785

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.