Evidence map›Paper›PMID 35189369›Full record

ReviewDrug discovery today2022

Nucleosides and emerging viruses: A new story.

Vincent Roy, Luigi A Agrofoglio

Abstract readReview
In one paragraph

Review in Drug discovery today, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

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  16. Anti-CMV therapy, what next? A systematic review.Frontiers in microbiology · 2023
    Review
  17. Article
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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

2 authors.

Vincent RoyICOA, University of Orléans, CNRS UMR 7311, Rue de Chartres, 45067 Orléans, France.
Luigi A AgrofoglioICOA, University of Orléans, CNRS UMR 7311, Rue de Chartres, 45067 Orléans, France. Electronic address: luigi.agrofoglio@univ-orleans.fr.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

With several US Food and Drug Administration (FDA)-approved drugs and high barriers to resistance, nucleoside and nucleotide analogs remain the cornerstone of antiviral therapies for not only herpesviruses, but also HIV and hepatitis viruses (B and C); however, with the exception of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), for which vaccines have been developed at unprecedented speed, there are no vaccines or small antivirals yet available for (re)emerging viruses, which are primarily RNA viruses. Thus, herein, we present an overview of ribonucleoside analogs recently developed and acting as inhibitors of the viral RNA-dependent RNA polymerase (RdRp). They are new lead structures that will be exploited for the discovery of new antiviral nucleosides.

Indexed as

Antiviral AgentsNucleosidesHumansRNA-Dependent RNA PolymeraseUnited StatesAntiviral AgentsNucleosidesRNA-Dependent RNA PolymeraseAntiviral therapyBroad-spectrum antiviral agentsNucleoside analogues(Re)emerging RNA virusesRNA-dependent RNA polymerase (RdRp)

Identifiers

PMID35189369
PMCPMC8856764

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.