Evidence map›Paper›PMID 38786134›Full record

ArticleAntibiotics (Basel, Switzerland)2024

Antifungal Activity of Brilacidin, a Nonpeptide Host Defense Molecule.

David J Larwood, David A Stevens

Abstract read
In one paragraph

Article in Antibiotics (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Cellular and molecular responses ofMicrobiology spectrum · 2026
    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

2 authors.

David J LarwoodDepartment of Pharmaceutical Chemistry, University of California-San Francisco, San Francisco, CA 94158, USA.ORCID 0000-0001-8202-0483
David A StevensCalifornia Institute for Medical Research, San Jose, CA 95128, USA.ORCID 0000-0002-5861-5716

Funding

David and Mary Larwood Family Charitable Fund Undirected general supportFoundation for Research in Infectious Diseases unspecifiedInnovation Pharmaceuticals Corporate funding, drug supplyUniversity of California San Francisco Medical Center unspecifiedValley Fever Americas Foundation unspecifiedValley Fever Solutions Unspecified
6 · The paper itself

Abstract

Natural host defensins, also sometimes termed antimicrobial peptides, are evolutionarily conserved. They have been studied as antimicrobials, but some pharmaceutical properties, undesirable for clinical use, have led to the development of synthetic molecules with constructed peptide arrangements and/or peptides not found in nature. The leading development currently is synthetic small-molecule nonpeptide mimetics, whose physical properties capture the characteristics of the natural molecules and share their biological attributes. We studied brilacidin, an arylamide of this type, for its activity in vitro against fungi (40 clinical isolates, 20 species) that the World Health Organization has highlighted as problem human pathogens. We found antifungal activity at low concentrations for many pathogens, which indicates that further screening for activity, particularly in vivo, is justified to evaluate this compound, and other mimetics, as attractive leads for the development of effective antifungal agents.

Indexed as

AMPantifungal activityantimicrobial peptidesbrilacidindefensinssynthetic nonpeptide mimetics

Identifiers

PMID38786134
PMCPMC11117233

What OpenQuestion holds

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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.