Evidence map›Paper›PMID 29545578›Full record

ArticleScientific reports2018

Exploring Ugi-Azide Four-Component Reaction Products for Broad-Spectrum Influenza Antivirals with a High Genetic Barrier to Drug Resistance.

Jiantao Zhang, Yanmei Hu, Christopher Foley, Yuanxiang Wang, Rami Musharrafieh, Shuting Xu, Yongtao Zhang, Chunlong Ma, Christopher Hulme, Jun Wang

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

16 citing papers in PubMed, 34 citations in OpenAlex.

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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

10 authors at 1 institution in 1 country.

Jiantao ZhangDepartment of Pharmacology and Toxicology, College of Pharmacy, The University of Arizona, Tucson, Arizona, 85721, United States.
Yanmei HuDepartment of Pharmacology and Toxicology, College of Pharmacy, The University of Arizona, Tucson, Arizona, 85721, United States.
Christopher FoleyDepartment of Chemistry and Biochemistry, The University of Arizona, Tucson, Arizona, 85721, United States.
Yuanxiang WangDepartment of Pharmacology and Toxicology, College of Pharmacy, The University of Arizona, Tucson, Arizona, 85721, United States.
Rami MusharrafiehDepartment of Chemistry and Biochemistry, The University of Arizona, Tucson, Arizona, 85721, United States.
Shuting XuDepartment of Chemistry and Biochemistry, The University of Arizona, Tucson, Arizona, 85721, United States.
Yongtao ZhangDepartment of Chemistry and Biochemistry, The University of Arizona, Tucson, Arizona, 85721, United States.
Chunlong MaBIO5 Institute, The University of Arizona, Tucson, Arizona, 85721, United States.
Christopher HulmeDepartment of Chemistry and Biochemistry, The University of Arizona, Tucson, Arizona, 85721, United States.
Jun WangDepartment of Pharmacology and Toxicology, College of Pharmacy, The University of Arizona, Tucson, Arizona, 85721, United States. junwang@pharmacy.arizona.edu.ORCID 0000-0002-4845-4621
University of Arizona · US

Funding

CHEMISTRY-BIOLOGY INTERFACE TRAINING PROGRAMT32GM008804 · NIGMS · UNIVERSITY OF ARIZONA · PI MONTFORT, WILLIAM R. · 2003 to 2023
$3.9M
Drug Discovery Targeting the Influenza A Virus M2-S31N Proton ChannelR33AI119187 · NIAID · UNIVERSITY OF ARIZONA · PI PEREZ, DANIEL R, WANG, JUN · 2017 to 2019
$1.2M
Drug Discovery Targeting the Influenza A Virus M2-S31N Proton ChannelR21AI119187 · NIAID · UNIVERSITY OF ARIZONA · PI PEREZ, DANIEL R, WANG, JUN · 2015 to 2016
$419k
NIAID NIH HHS R21 AI119187NIAID NIH HHS R33 AI119187NIGMS NIH HHS T32 GM008804
6 · The paper itself

Abstract

Influenza viruses are respiratory pathogens that are responsible for seasonal influenza and sporadic influenza pandemic. The therapeutic efficacy of current influenza vaccines and small molecule antiviral drugs is limited due to the emergence of multidrug-resistant influenza viruses. In response to the urgent need for the next generation of influenza antivirals, we utilized a fast-track drug discovery platform by exploring multi-component reaction products for antiviral drug candidates. Specifically, molecular docking was applied to screen a small molecule library derived from the Ugi-azide four-component reaction methodology for inhibitors that target the influenza polymerase PA

Indexed as

Drug DiscoveryA549 CellsAntiviral AgentsAzidesCell SurvivalDrug Resistance, ViralGenome, ViralGenotypeHumansInfluenza A virusInfluenza, HumanMolecular Docking SimulationSmall Molecule LibrariesStructure-Activity RelationshipVirus ReplicationAntiviral AgentsAzidesSmall Molecule Libraries

Identifiers

PMID29545578
PMCPMC5854701
OpenAlexW2805402587

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.