Evidence map›Paper›PMID 32723801›Full record

ReviewThe Journal of pharmacology and experimental therapeutics2020

Drug Discovery Strategies for SARS-CoV-2.

Zeenat A Shyr, Kirill Gorshkov, Catherine Z Chen, Wei Zheng

Open access · bronzeAbstract readReview
In one paragraph

Review in The Journal of pharmacology and experimental therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed
2.5field-weighted citation impact, top 6% 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

57 citing papers in PubMed, 107 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. In Silico Design of New Dual Inhibitors of SARS-CoV-2 MInternational journal of molecular sciences · 2023
    Article
  8. Article
  9. Article
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  11. Article
  12. Article
  13. Article
  14. Article
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  17. Article
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  19. Review
  20. 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

4 authors at 1 institution in 1 country.

Zeenat A ShyrNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland.
Kirill GorshkovNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland.
Catherine Z ChenNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland.
Wei ZhengNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, Maryland wzheng@mail.nih.gov.
National Center for Advancing Translational Sciences · US

Funding

Drug Repurposing Screening for Rare and Neglected DiseasesZIATR000018 · NCATS · NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES · PI ZHENG, WEI · 2015 to 2025
$24.6M
COVID-19: Identification and Development of Clinical Candidates to Treat SARS-CoV-2 ZIATR000422 · NCATS · NATIONAL CENTER FOR ADVANCING TRANSLATIONAL SCIENCES · PI LO, DONALD · 2020 to 2021
$3.3M
Intramural NIH HHS ZIA TR000018Intramural NIH HHS ZIA TR000422
6 · The paper itself

Abstract

Coronavirus disease 2019 (COVID-19) is a novel disease caused by the severe acute respiratory syndrome coronavirus (SARS-CoV)-2 virus that was first detected in December of 2019 in Wuhan, China, and has rapidly spread worldwide. The search for a suitable vaccine as well as effective therapeutics for the treatment of COVID-19 is underway. Drug repurposing screens provide a useful and effective solution for identifying potential therapeutics against SARS-CoV-2. For example, the experimental drug remdesivir, originally developed for Ebola virus infections, has been approved by the US Food and Drug Administration as an emergency use treatment of COVID-19. However, the efficacy and toxicity of this drug need further improvements. In this review, we discuss recent findings on the pathology of coronaviruses and the drug targets for the treatment of COVID-19. Both SARS-CoV-2-specific inhibitors and broad-spectrum anticoronavirus drugs against SARS-CoV, Middle East respiratory syndrome coronavirus, and SARS-CoV-2 will be valuable additions to the anti-SARS-CoV-2 armament. A multitarget treatment approach with synergistic drug combinations containing different mechanisms of action may be a practical therapeutic strategy for the treatment of severe COVID-19. SIGNIFICANCE STATEMENT: Understanding the biology and pathology of RNA viruses is critical to accomplish the challenging task of developing vaccines and therapeutics against SARS-CoV-2. This review highlights the anti-SARS-CoV-2 drug targets and therapeutic development strategies for COVID-19 treatment.

Indexed as

Antiviral AgentsBetacoronavirusClinical Trials as TopicCoronavirus InfectionsCOVID-19COVID-19 VaccinesDrug DiscoveryHumansPandemicsPneumonia, ViralSARS-CoV-2Viral VaccinesVirus InternalizationVirus ReplicationAntiviral AgentsCOVID-19 VaccinesViral Vaccines

Identifiers

PMID32723801
PMCPMC7569306
OpenAlexW3045498627

What OpenQuestion 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 OpenQuestion graph.