Evidence map›Paper›PMID 39860254›Full record

ArticleMolecules (Basel, Switzerland)2025

6-Bromoindole- and 6-Bromoindazole-Based Inhibitors of Bacterial Cystathionine γ-Lyase Containing 3-Aminothiophene-2-Carboxylate Moiety.

Roman A Novikov, Dmitry N Platonov, Alexander Yu Belyy, Konstantin V Potapov, Maxim A Novikov, Yury V Tomilov, Olga I Kechko, Tatiana A Seregina, Anastasia S Zemskaya, Pavel N Solyev and 1 more

Abstract read
In one paragraph

Article in Molecules (Basel, Switzerland), 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

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

11 authors.

Roman A NovikovEngelhardt Institute of Molecular Biology of the Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia.
Dmitry N PlatonovZelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, 47 Leninsky Avenue, Moscow 119991, Russia.ORCID 0000-0002-9331-7319
Alexander Yu BelyyZelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, 47 Leninsky Avenue, Moscow 119991, Russia.ORCID 0000-0002-4948-6238
Konstantin V PotapovEngelhardt Institute of Molecular Biology of the Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia.ORCID 0000-0003-3819-2418
Maxim A NovikovEngelhardt Institute of Molecular Biology of the Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia.ORCID 0000-0002-7259-494X
Yury V TomilovZelinsky Institute of Organic Chemistry of the Russian Academy of Sciences, 47 Leninsky Avenue, Moscow 119991, Russia.ORCID 0000-0002-3433-7571
Olga I KechkoEngelhardt Institute of Molecular Biology of the Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia.
Tatiana A SereginaEngelhardt Institute of Molecular Biology of the Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia.ORCID 0000-0003-3278-0390
Anastasia S ZemskayaEngelhardt Institute of Molecular Biology of the Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia.ORCID 0000-0002-0332-5105
Pavel N SolyevEngelhardt Institute of Molecular Biology of the Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia.ORCID 0000-0002-5546-4975
Vladimir A MitkevichEngelhardt Institute of Molecular Biology of the Russian Academy of Sciences, 32 Vavilov St., Moscow 119991, Russia.ORCID 0000-0002-1517-1983

Funding

Ministry of Science and Higher Education of the Russian Federation agreement No. 075-10-2021-113, unique project ID RF----193021X0001
6 · The paper itself

Abstract

In recent years, a number of synthetic potentiators of antibiotics have been discovered. Their action can significantly enhance the antibacterial effect and limit the spread of antibiotic resistance through inhibition of bacterial cystathionine-γ-lyase. To expand the known set of potentiators, we developed methods for the synthesis of five new representatives of 6-bromoindole derivatives-potential inhibitors of bacterial cystathionine-γ-lyase-namely potassium 3-amino-5-((6-bromoindolyl)methyl)thiophene-2-carboxylate (

Indexed as

Anti-Bacterial AgentsCystathionine gamma-LyaseEnzyme InhibitorsIndazolesIndolesThiophenesMicrobial Sensitivity TestsMolecular StructureStructure-Activity RelationshipAnti-Bacterial AgentsCystathionine gamma-LyaseEnzyme InhibitorsIndazolesIndolesThiophenes6-bromoindazole6-bromoindoleantibiotic potentiators

Identifiers

PMID39860254
PMCPMC11767297

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Registered trials

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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.