Evidence map›Paper›PMID 27059228›Full record

ArticleAntiviral research2016

Novel diversity-oriented synthesis-derived respiratory syncytial virus inhibitors identified via a high throughput replicon-based screen.

Jeremy R Duvall, Lynn VerPlank, Barbara Ludeke, Sarah M McLeod, Maurice D Lee, Karthick Vishwanathan, Carol A Mulrooney, Sebastian Le Quement, Qin Yu, Michelle A Palmer and 4 more

Open access · greenAbstract read
In one paragraph

Article in Antiviral research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Review
  3. Viral Replicon Systems and Their Biosafety Aspects.Applied biosafety : journal of the American Biological Safety Association · 2023
    Review
  4. Article
  5. Article
  6. Article
  7. Review
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

14 authors at 3 institutions in 1 country.

Jeremy R DuvallBroad Institute of MIT and Harvard, 415 Main St., Cambridge, MA 02142, United States.
Lynn VerPlankBroad Institute of MIT and Harvard, 415 Main St., Cambridge, MA 02142, United States.
Barbara LudekeBoston University School of Medicine, 72 East Concord Street, Boston, MA 02118, United States.
Sarah M McLeodAstraZeneca R&D Boston, Infection Innovative Medicines Unit, 35 Gatehouse Drive, Waltham, MA 02451, United States.
Maurice D LeeBroad Institute of MIT and Harvard, 415 Main St., Cambridge, MA 02142, United States.
Karthick VishwanathanAstraZeneca R&D Boston, Early Clinical Development, 35 Gatehouse Drive, Waltham, MA 02451, United States.
Carol A MulrooneyBroad Institute of MIT and Harvard, 415 Main St., Cambridge, MA 02142, United States.
Sebastian Le QuementBroad Institute of MIT and Harvard, 415 Main St., Cambridge, MA 02142, United States.
Qin YuAstraZeneca R&D Boston, Infection Innovative Medicines Unit, 35 Gatehouse Drive, Waltham, MA 02451, United States.
Michelle A PalmerBroad Institute of MIT and Harvard, 415 Main St., Cambridge, MA 02142, United States.
Paul FlemingAstraZeneca R&D Boston, Infection Innovative Medicines Unit, 35 Gatehouse Drive, Waltham, MA 02451, United States.
Rachel FearnsBoston University School of Medicine, 72 East Concord Street, Boston, MA 02118, United States.
Michael A FoleyBroad Institute of MIT and Harvard, 415 Main St., Cambridge, MA 02142, United States.
Christina A SchererBroad Institute of MIT and Harvard, 415 Main St., Cambridge, MA 02142, United States. Electronic address: cscherer@alum.mit.edu.
Broad Institute · USAstraZeneca (United States) · USBoston University · US

Funding

Initiation and regulation of RSV mRNA transcription and genome replicationR01AI113321 · NIAID · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FEARNS, RACHEL · 2014 to 2017
$1.7M
NIAID NIH HHS R01 AI113321
6 · The paper itself

Abstract

Respiratory syncytial virus (RSV) infections affect millions of children and adults every year. Despite the significant disease burden, there are currently no safe and effective vaccines or therapeutics. We employed a replicon-based high throughput screen combined with live-virus triaging assays to identify three novel diversity-oriented synthesis-derived scaffolds with activity against RSV. One of these small molecules is shown to target the RSV polymerase (L protein) to inhibit viral replication and transcription; the mechanisms of action of the other small molecules are currently unknown. The compounds described herein may provide attractive inhibitors for lead optimization campaigns.

Indexed as

Microbial Sensitivity TestsAntiviral AgentsDrug DiscoveryHep G2 CellsHigh-Throughput Screening AssaysHumansRepliconRespiratory Syncytial Virus, HumanRespiratory Syncytial Virus InfectionsRNA-Dependent RNA PolymeraseViral ProteinsVirus ReplicationAntiviral AgentsRNA-Dependent RNA PolymeraseViral ProteinsDiversity-oriented synthesisRepliconRespiratory syncytial virus

Identifiers

PMID27059228
PMCPMC4937797
OpenAlexW2318026359

What OpenQuestion holds

Textmetadata
LicenceTDM
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.