Evidence map›Paper›PMID 34379382›Full record

ArticleACS infectious diseases2021

Mechanistic Duality of Bacterial Efflux Substrates and Inhibitors: Example of Simple Substituted Cinnamoyl and Naphthyl Amides.

Napoleon D'Cunha, Mohammad Moniruzzaman, Keith Haynes, Giuliano Malloci, Connor J Cooper, Enrico Margiotta, Attilio V Vargiu, Muhammad R Uddin, Inga V Leus, Feng Cao and 5 more

Open access · greenAbstract read
In one paragraph

Article in ACS infectious diseases, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

10 citing papers in PubMed, 24 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

15 authors at 5 institutions in 2 countries.

Napoleon D'CunhaDepartment of Pharmacology and Physiology, Saint Louis University School of Medicine, St. Louis, Missouri 63110, United States.
Mohammad MoniruzzamanDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73072, United States.
Keith HaynesDepartment of Pharmacology and Physiology, Saint Louis University School of Medicine, St. Louis, Missouri 63110, United States.
Giuliano MallociDepartment of Physics, University of Cagliari, Monserrato, Cagliari 09042, Italy.ORCID 0000-0002-5985-257X
Connor J CooperGraduate School of Genome Science and Technology, University of Tennessee, Knoxville, Tennessee 37996, United States.ORCID 0000-0002-5527-9948
Enrico MargiottaDepartment of Physics, University of Cagliari, Monserrato, Cagliari 09042, Italy.ORCID 0000-0003-4790-021X
Attilio V VargiuDepartment of Physics, University of Cagliari, Monserrato, Cagliari 09042, Italy.ORCID 0000-0003-4013-8867
Muhammad R UddinDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73072, United States.
Inga V LeusDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73072, United States.
Feng CaoJohn Cochran Division, Department of Veteran Affairs Medical Center, St. Louis, Missouri 63106, United States.ORCID 0000-0002-4820-6628
Jerry M ParksBiosciences Division, Oak Ridge National Laboratory, Oak Ridge, Tennessee 37831, United States.ORCID 0000-0002-3103-9333
Valentin V RybenkovDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73072, United States.ORCID 0000-0002-5300-4369
Paolo RuggeroneDepartment of Physics, University of Cagliari, Monserrato, Cagliari 09042, Italy.ORCID 0000-0003-0825-0824
Helen I ZgurskayaDepartment of Chemistry and Biochemistry, University of Oklahoma, Norman, Oklahoma 73072, United States.ORCID 0000-0001-8929-4727
John K WalkerDepartment of Pharmacology and Physiology, Saint Louis University School of Medicine, St. Louis, Missouri 63110, United States.ORCID 0000-0002-8683-0026
University of Oklahoma · USUniversity of Cagliari · ITSaint Louis University · USOak Ridge National Laboratory · USJohn Cochran VA Medical Center · US

Funding

Transport across two membranes by AcrAB-TolC complexR01AI052293 · NIAID · UNIVERSITY OF OKLAHOMA NORMAN · PI ZGURSKAYA, HELEN I · 2003 to 2024
$7.7M
Optimization of efflux avoidance and inhibition for antibiotic developmentR01AI136799 · NIAID · UNIVERSITY OF OKLAHOMA · PI GNANAKARAN, SANDRASEGARAM, RUGGERONE, PAOLO · 2018 to 2022
$5.7M
Transport Across Two Membranes by AcrAB-TolC ComplexR56AI052293 · NIAID · UNIVERSITY OF OKLAHOMA · PI ZGURSKAYA, HELEN I · 2008 to 2008
$360k
Biacore T200S10OD025014 · OD · OKLAHOMA MEDICAL RESEARCH FOUNDATION · PI MCEVER, RODGER PAUL · 2018 to 2018
$322k
NIAID NIH HHS R01 AI052293NIAID NIH HHS R01 AI136799NIAID NIH HHS R56 AI052293NIH HHS S10 OD025014
6 · The paper itself

Abstract

Antibiotic resistance poses an immediate and growing threat to human health. Multidrug efflux pumps are promising targets for overcoming antibiotic resistance with small-molecule therapeutics. Previously, we identified a diaminoquinoline acrylamide, NSC-33353, as a potent inhibitor of the AcrAB-TolC efflux pump in

Indexed as

Escherichia coli ProteinsAmidesATP-Binding Cassette, Sub-Family C ProteinsEscherichia coliHumansMolecular Docking SimulationAcrB protein, E coliAmidesATP-Binding Cassette, Sub-Family C ProteinsEscherichia coli ProteinsAcrAB−TolCantibiotic permeationantibiotic potentiationefflux pump inhibitorsEscherichia coli

Identifiers

PMID34379382
PMCPMC8668026
OpenAlexW3189515306

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.