Evidence map›Paper›PMID 42023066›Full record

ReviewRSC chemical biology2026

Leveraging the lipoprotein trafficking pathway for the development of novel antimicrobials.

Haley B Gartrell, Taryn Trigler, Marcin Grabowicz, William M Wuest

Abstract readReview
In one paragraph

Review in RSC chemical biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Haley B GartrellDepartment of Chemistry, Emory University 1515 Dickey Drive Atlanta GA USA wwuest@emory.edu.
Taryn TriglerDepartment of Microbiology & Immunology, Emory University School of Medicine Atlanta GA USA marcin.grabowicz@emory.edu.ORCID https://orcid.org/0009-0000-4800-1641
Marcin GrabowiczDepartment of Microbiology & Immunology, Emory University School of Medicine Atlanta GA USA marcin.grabowicz@emory.edu.
William M WuestDepartment of Chemistry, Emory University 1515 Dickey Drive Atlanta GA USA wwuest@emory.edu.ORCID https://orcid.org/0000-0002-5198-7744

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antimicrobial resistance continues to limit the number of effective antimicrobials to treat bacterial infections. The development of antimicrobials with unique mechanisms of action is crucial to overcoming this threat. By employing various methods of hit identification, such as artificial intelligence, whole-cell screening, and drug repurposing, small-molecules that display activity against bacterial pathogens can be identified. Herein, four molecules (abaucin, enterololin, lolamicin, and fendiline) that were found to have high potency against either

Identifiers

PMID42023066
PMCPMC13097052

What Socratic 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 Socratic graph.