Evidence map›Paper›PMID 29870771›Full record

ArticleAntiviral research2018

Identification of a small molecule inhibitor of Ebola virus genome replication and transcription using in silico screening.

Victoria Easton, Martin McPhillie, Isabel Garcia-Dorival, John N Barr, Thomas A Edwards, Richard Foster, Colin Fishwick, Mark Harris

Open access · hybridAbstract read
In one paragraph

Article in Antiviral research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

12 citing papers in PubMed, 18 citations in OpenAlex.

  1. Discovery of three small-molecule inhibitors targetingThe Journal of general virology · 2025
    Article
  2. Marburg Virus Minigenome Assays.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Anno 2021: Which antivirals for the coming decade?Annual reports in medicinal chemistry · 2021
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. 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

8 authors at 2 institutions in 1 country.

Victoria EastonSchool of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK; Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, UK.
Martin McPhillieSchool of Chemistry, Faculty of Mathematics and Physical Sciences, University of Leeds, Leeds LS2 9JT, UK; Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, UK.
Isabel Garcia-DorivalInstitute of Infection and Global Health, University of Liverpool, Liverpool L3 5RF, UK.
John N BarrSchool of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK; Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, UK.
Thomas A EdwardsSchool of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK; Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, UK.
Richard FosterSchool of Chemistry, Faculty of Mathematics and Physical Sciences, University of Leeds, Leeds LS2 9JT, UK; Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, UK.
Colin FishwickSchool of Chemistry, Faculty of Mathematics and Physical Sciences, University of Leeds, Leeds LS2 9JT, UK; Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, UK. Electronic address: c.w.g.fishwick@leeds.ac.uk.
Mark HarrisSchool of Molecular and Cellular Biology, Faculty of Biological Sciences, University of Leeds, Leeds LS2 9JT, UK; Astbury Centre for Structural Molecular Biology, University of Leeds, Leeds LS2 9JT, UK. Electronic address: m.harris@leeds.ac.uk.
University of Leeds · GBUniversity of Liverpool · GB

Funding

Wellcome Trust 109713/Z/15/Z
6 · The paper itself

Abstract

Ebola virus (EBOV) causes a severe haemorrhagic fever in humans and has a mortality rate over 50%. With no licensed drug treatments available, EBOV poses a significant threat. Investigations into possible therapeutics have been severely hampered by the classification of EBOV as a BSL4 pathogen. Here, we describe a drug discovery pathway combining in silico screening of compounds predicted to bind to a hydrophobic pocket on the nucleoprotein (NP); with a robust and rapid EBOV minigenome assay for inhibitor validation at BSL2. One compound (MCCB4) was efficacious (EC

Indexed as

AnimalsAntiviral AgentsCell LineDrug Evaluation, PreclinicalEbolavirusMolecular Dynamics SimulationNucleoproteinsProtein BindingTranscription, GeneticViral ProteinsVirus ReplicationAntiviral AgentsNucleoproteinsViral ProteinsDrug discoveryEbola virus (EBOV)MinigenomeNucleoprotein (NP)Small molecule inhibitors (SMIs)

Identifiers

PMID29870771
PMCPMC6371959
OpenAlexW2806916224

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.