Evidence map›Paper›PMID 35210534›Full record

ArticleCommunications biology2022

An amiloride derivative is active against the F

Kiel Hards, Chen-Yi Cheung, Natalie Waller, Cara Adolph, Laura Keighley, Zhi Shean Tee, Liam K Harold, Ayana Menorca, Richard S Bujaroski, Benjamin J Buckley and 12 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.2field-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

21 citing papers in PubMed, 41 citations in OpenAlex.

  1. Article
  2. Metabolic perturbation reduces antibiotic tolerance inMicrobiology (Reading, England) · 2026
    Article
  3. Article
  4. Article
  5. Carbon Monoxide and Prokaryotic Energy Metabolism.International journal of molecular sciences · 2025
    Review
  6. Review
  7. Antibiotics (Basel, Switzerland) · 2024
    Review
  8. Article
  9. CytochromeRSC medicinal chemistry · 2024
    Review
  10. Quinoline Compounds Targeting theACS infectious diseases · 2023
    Article
  11. Review
  12. Review
  13. Article
  14. Frontiers in immunology · 2023
    Review
  15. Article
  16. Article
  17. Response ofInternational journal of molecular sciences · 2022
    Article
  18. Article
  19. Bioenergetics and Reactive Nitrogen Species in Bacteria.International journal of molecular sciences · 2022
    Review
  20. Article
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

22 authors at 7 institutions in 6 countries.

Kiel Hards *Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Chen-Yi Cheung *Department of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Natalie WallerDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Cara AdolphDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Laura KeighleyDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Zhi Shean TeeDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Liam K HaroldDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Ayana MenorcaDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Richard S BujaroskiMolecular Horizons and School of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, Australia.ORCID http://orcid.org/0000-0002-8459-527X
Benjamin J BuckleyMolecular Horizons and School of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, Australia.
Joel D A TyndallSchool of Pharmacy, University of Otago, Dunedin, New Zealand.ORCID http://orcid.org/0000-0003-0783-1635
Matthew B McNeilDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand.
Kyu Y RheeWeill Department of Medicine, Weill Cornell Medical College, New York, NY, USA.ORCID http://orcid.org/0000-0003-4582-2895
Helen K Opel-ReadingDepartment of Biochemistry, University of Otago, Dunedin, New Zealand.
Kurt KrauseMaurice Wilkins Centre for Molecular Biodiscovery, The University of Otago, Dunedin, New Zealand.ORCID http://orcid.org/0000-0002-3525-1112
Laura PreissDepartment of Structural Biology, Max-Planck Institute of Biophysics, Frankfurt am Main, Germany.
Julian D LangerDepartment of Molecular Membrane Biology, Max-Planck Institute of Biophysics, Frankfurt am Main, Germany.ORCID http://orcid.org/0000-0002-5190-577X
Thomas MeierDepartment of Life Sciences, Imperial College London, London, UK.ORCID http://orcid.org/0000-0003-3364-3320
Erik J HasenoehrlDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, New York, NY, USA.
Michael BerneyDepartment of Microbiology and Immunology, Albert Einstein College of Medicine, New York, NY, USA.ORCID http://orcid.org/0000-0002-4833-0573
Michael J KelsoMolecular Horizons and School of Chemistry and Molecular Bioscience, University of Wollongong, Wollongong, Australia. mkelso@uow.edu.au.ORCID http://orcid.org/0000-0001-7809-6637
Gregory M CookDepartment of Microbiology and Immunology, University of Otago, Dunedin, New Zealand. Greg.cook@otago.ac.nz.ORCID http://orcid.org/0000-0001-8349-1500
University of Otago · NZMaurice Wilkins Centre · NZUniversity of Wollongong · AUAlbert Einstein College of Medicine · USMax Planck Institute of Biophysics · DECornell University · USPrivate University in the Principality of Liechtenstein · LI

Funding

Eradicating persistent M. tuberculosis by synthetic lethality of terminal respiratory oxidasesR01AI139465 · NIAID · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI BERNEY, MICHAEL · 2019 to 2023
$3.2M
NIAID NIH HHS R01 AI139465Wellcome Trust
6 · The paper itself

Abstract

Increasing antimicrobial resistance compels the search for next-generation inhibitors with differing or multiple molecular targets. In this regard, energy conservation in Mycobacterium tuberculosis has been clinically validated as a promising new drug target for combatting drug-resistant strains of M. tuberculosis. Here, we show that HM2-16F, a 6-substituted derivative of the FDA-approved drug amiloride, is an anti-tubercular inhibitor with bactericidal properties comparable to the FDA-approved drug bedaquiline (BDQ; Sirturo

Indexed as

Mycobacterium tuberculosisAdenosine TriphosphateAmilorideAntitubercular AgentsCytochromesElectron Transport Complex IVOxidoreductasesAdenosine TriphosphateAmilorideAntitubercular AgentsCytochromesElectron Transport Complex IVOxidoreductases

Identifiers

PMID35210534
PMCPMC8873251
OpenAlexW4213418852

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.