Evidence map›Paper›PMID 32660307›Full record

ReviewSLAS discovery : advancing life sciences R & D2020

RNA-Dependent RNA Polymerase as a Target for COVID-19 Drug Discovery.

Wei Zhu, Catherine Z Chen, Kirill Gorshkov, Miao Xu, Donald C Lo, Wei Zheng

Open access · hybridAbstract readReview
In one paragraph

Review in SLAS discovery : advancing life sciences R & D, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 94 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
94citing papers in PubMed, 3 pooled it
3.9field-weighted citation impact, top 4% 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

94 citing papers in PubMed, 3 syntheses or guidelines pooled it, 188 citations in OpenAlex.

  1. Pooled it
  2. The efficacy and adverse effects of favipiravir on patients with COVID-19: A systematic review and meta-analysis of published clinical trials and observational studies.International journal of infectious diseases : IJID : official publication of the International Society for Infectious Diseases · 2022
    Pooled it
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  17. Small Molecule Drugs Targeting Viral Polymerases.Pharmaceuticals (Basel, Switzerland) · 2024
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34 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

6 authors at 1 institution in 1 country.

Wei ZhuNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, USA.
Catherine Z ChenNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, USA.
Kirill GorshkovNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, USA.
Miao XuNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, USA.
Donald C LoNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, USA.
Wei ZhengNational Center for Advancing Translational Sciences, National Institutes of Health, Bethesda, MD, USA.ORCID 0000-0003-1034-0757
National Institutes of Health · 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
6 · The paper itself

Abstract

COVID-19 respiratory disease caused by the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) has rapidly become a global health issue since it emerged in December 2019. While great global efforts are underway to develop vaccines and to discover or repurpose therapeutic agents for this disease, as of this writing only the nucleoside drug remdesivir has been approved under Emergency Use Authorization to treat COVID-19. The RNA-dependent RNA polymerase (RdRP), a viral enzyme for viral RNA replication in host cells, is one of the most intriguing and promising drug targets for SARS-CoV-2 drug development. Because RdRP is a viral enzyme with no host cell homologs, selective SARS-CoV-2 RdRP inhibitors can be developed that have improved potency and fewer off-target effects against human host proteins and thus are safer and more effective therapeutics for treating COVID-19. This review focuses on biochemical enzyme and cell-based assays for RdRPs that could be used in high-throughput screening to discover new and repurposed drugs against SARS-CoV-2.

Indexed as

COVID-19 Drug TreatmentAdenosine MonophosphateAlanineAmidesAntiviral AgentsDrug DiscoveryEnzyme InhibitorsHigh-Throughput Screening AssaysHumansMiddle East Respiratory Syndrome CoronavirusPyrazinesRNA-Dependent RNA PolymeraseSARS-CoV-2Viral ProteinsVirus ReplicationAdenosine MonophosphateAlanineAmidesAntiviral AgentsEnzyme InhibitorsfavipiravirPyrazinesremdesivirRNA-Dependent RNA PolymeraseViral Proteinscoronavirus infectionCOVID-19RdRP assaysRdRP inhibitorsRNA-dependent RNA polymeraseSARS-CoV-2

Identifiers

PMID32660307
PMCPMC7684788
OpenAlexW3042238480

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.