Evidence map›Paper›PMID 39975250›Full record

ArticlebioRxiv : the preprint server for biology2025

1,2,4-Triazole-based first-in-class non-nucleoside inhibitors of bacterial enzyme MraY.

Tomayo Berida, Tzu-Yu Huang, Stefanie C Weck, Marcel Lutz, Samuel R McKee, Nathalie Kagerah, Destinee Manning, Mohamed E Jahan, Sushil K Mishra, Robert J Doerksen and 3 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

5 · Who and what money

Authors and funding

13 authors.

Tomayo Berida
Tzu-Yu Huang
Stefanie C Weck
Marcel Lutz
Samuel R McKee
Nathalie Kagerah
Destinee Manning
Mohamed E Jahan
Robert J Doerksen
Christina L Stallings
Christian Ducho
Sudeshna Roy

Funding

Development of 1,2,4-Triazolyl Compounds and their derivatives as a New Treatment for TuberculosisR01AI181316 · NIAID · WASHINGTON UNIVERSITY · PI Sudeshna Roy, Christina Leigh Stallings · 2024 to 2026
$2.3M
Target-based chemotherapeutics development against Mycobacterium tuberculosisR21AI142210 · NIAID · UNIVERSITY OF MISSISSIPPI · PI ROY, SUDESHNA · 2019 to 2020
$411k
NIAID NIH HHS R01 AI181316NIAID NIH HHS R21 AI142210
6 · The paper itself

Abstract

MraY, a bacterial enzyme crucial for the synthesis of peptidoglycans, represents a promising yet underexplored target for the development of effective antibacterial agents. Nature has provided several classes of nucleoside inhibitors of MraY and scientists have modified these structures further to obtain natural product-like inhibitors of MraY. The natural products and their synthetic analogs suffer from non-optimal Abstract Figure:

Identifiers

PMID39975250
PMCPMC11838528

What OpenQuestion holds

Textmetadata
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.