Evidence map›Paper›PMID 28087313›Full record

ArticleAntiviral research2017

An M2-V27A channel blocker demonstrates potent in vitro and in vivo antiviral activities against amantadine-sensitive and -resistant influenza A viruses.

Yanmei Hu, Rami Musharrafieh, Chunlong Ma, Jiantao Zhang, Donald F Smee, William F DeGrado, Jun Wang

Open access · greenAbstract read
In one paragraph

Article in Antiviral research, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

36 citing papers in PubMed, 52 citations in OpenAlex.

  1. Review
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  7. Antiviral Approaches against Influenza Virus.Clinical microbiology reviews · 2023
    Review
  8. Review
  9. MicroRNA-205-5p: A potential therapeutic target for influenza A.Journal of cellular and molecular medicine · 2022
    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

7 authors at 3 institutions in 1 country.

Yanmei Hu *Department of Pharmacology and Toxicology, College of Pharmacy, The University of Arizona, Tucson, Arizona 85721, United States.
Rami Musharrafieh *Department 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.
Jiantao ZhangDepartment of Pharmacology and Toxicology, College of Pharmacy, The University of Arizona, Tucson, Arizona 85721, United States.
Donald F SmeeInstitute for Antiviral Research, Department of Animal, Dairy and Veterinary Sciences, Utah State University, Logan, Utah 84322, United States.
William F DeGradoDepartment of Pharmaceutical Chemistry, School of Pharmacy, University of California, San Francisco, California 94158, United States.
Jun WangDepartment of Pharmacology and Toxicology, College of Pharmacy, The University of Arizona, Tucson, Arizona 85721, United States.
University of Arizona · USUniversity of California, San Francisco · USUtah State University · US

Funding

Structure of M2 Proton Channel from Influenza A VirusR01GM056423 · NIGMS · UNIVERSITY OF PENNSYLVANIA · PI DEGRADO, WILLIAM · 1997 to 2016
$4.5M
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 HHSN272201000039CNIAID NIH HHS HHSN272201000039INIAID NIH HHS R21 AI119187NIAID NIH HHS R33 AI119187NIGMS NIH HHS R01 GM056423NIGMS NIH HHS T32 GM008804
6 · The paper itself

Abstract

Adamantanes such as amantadine (1) and rimantadine (2) are FDA-approved anti-influenza drugs that act by inhibiting the wild-type M2 proton channel from influenza A viruses, thereby inhibiting the uncoating of the virus. Although adamantanes have been successfully used for more than four decades, their efficacy was curtailed by emerging drug resistance. Among the limited number of M2 mutants that confer amantadine resistance, the M2-V27A mutant was found to be the predominant mutant under drug selection pressure, thereby representing a high profile antiviral drug target. Guided by molecular dynamics simulations, we previously designed first-in-class M2-V27A inhibitors. One of the potent lead compounds, spiroadamantane amine (3), inhibits both the M2-WT and M2-V27A mutant with IC

Indexed as

Drug Resistance, ViralAdamantaneAmantadineAnimalsAntiviral AgentsDogsHumansInfluenza A virusInfluenza, HumanInhibitory Concentration 50Madin Darby Canine Kidney CellsMolecular Dynamics SimulationMutationOrthomyxoviridae InfectionsSpiro CompoundsStructure-Activity RelationshipAdamantaneAmantadineAntiviral AgentsM2 protein, Influenza A virusspiroadamantane amineSpiro CompoundsViral Matrix ProteinsViroporin ProteinsAntiviralDrug resistanceInfluenza virusM2 proton channelSpiroadamantaneV27A

Identifiers

PMID28087313
PMCPMC5326599
OpenAlexW2568695891

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.