Evidence map›Paper›PMID 30206124›Full record

ArticleThe Journal of biological chemistry2018

Development of an allosteric inhibitor class blocking RNA elongation by the respiratory syncytial virus polymerase complex.

Robert M Cox, Mart Toots, Jeong-Joong Yoon, Julien Sourimant, Barbara Ludeke, Rachel Fearns, Elyse Bourque, Joseph Patti, Edward Lee, John Vernachio and 1 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 34 citations in OpenAlex.

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  12. Facile Synthesis of Homodimeric Protein Ligands.Chembiochem : a European journal of chemical biology · 2023
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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

11 authors at 2 institutions in 1 country.

Robert M CoxFrom the Institute for Biomedical Sciences, Georgia State University, Atlanta, Georgia 30303.
Mart TootsFrom the Institute for Biomedical Sciences, Georgia State University, Atlanta, Georgia 30303.
Jeong-Joong YoonFrom the Institute for Biomedical Sciences, Georgia State University, Atlanta, Georgia 30303.
Julien SourimantFrom the Institute for Biomedical Sciences, Georgia State University, Atlanta, Georgia 30303.
Barbara Ludekethe Department of Microbiology, Boston University School of Medicine, Boston, Massachusetts 02118, and.
Rachel Fearnsthe Department of Microbiology, Boston University School of Medicine, Boston, Massachusetts 02118, and.
Elyse Bourque
Joseph PattiAviragen Therapeutics, Alpharetta, Georgia 30009.
Edward LeeAviragen Therapeutics, Alpharetta, Georgia 30009.
John VernachioAviragen Therapeutics, Alpharetta, Georgia 30009.
Richard K PlemperFrom the Institute for Biomedical Sciences, Georgia State University, Atlanta, Georgia 30303, rplemper@gsu.edu.
Georgia State University · USBoston University · US

Funding

BIOLOGY OF THE LUNG--MULTIDISCIPLINARY PROGRAMT32HL007035 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Darrell N. Kotton, JOSEPH P MIZGERD · 1985 to 2026
$24.3M
Identification and Pre-Clinical Evaluation of Measles Virus InhibitorsR01AI071002 · NIAID · GEORGIA STATE UNIVERSITY · PI PLEMPER, RICHARD K. · 2006 to 2022
$6.6M
Novel Therapeutics against Respiratory Syncytial Virus InfectionR01HD079327 · NICHD · GEORGIA STATE UNIVERSITY · PI PLEMPER, RICHARD K. · 2014 to 2018
$2.8M
NHLBI NIH HHS T32 HL007035NIAID NIH HHS R01 AI071002NICHD NIH HHS R01 HD079327
6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) represents a significant health threat to infants and to elderly or immunocompromised individuals. There are currently no vaccines available to prevent RSV infections, and disease management is largely limited to supportive care, making the identification and development of effective antiviral therapeutics against RSV a priority. To identify effective chemical scaffolds for managing RSV disease, we conducted a high-throughput anti-RSV screen of a 57,000-compound library. We identified a hit compound that specifically blocked activity of the RSV RNA-dependent RNA polymerase (RdRp) complex, initially with moderate low-micromolar potency. Mechanistic characterization in an

Indexed as

Allosteric RegulationAnimalsAntiviral AgentsCells, CulturedHumansMaleMiceRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsRNA-Dependent RNA PolymeraseTranscription, GeneticViral ProteinsVirus ReplicationAntiviral AgentsRNA-Dependent RNA PolymeraseViral Proteinsanimal virusantiviral agentdrug developmentmedicinal chemistryRdRprespiratory diseaserespiratory syncytial virusRNA-dependent RNA polymeraseviral polymerase

Identifiers

PMID30206124
PMCPMC6204889
OpenAlexW2891166015

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.