Evidence map›Paper›PMID 35163756›Full record

ArticleInternational journal of molecular sciences2022

Drug Repurposing of the Unithiol: Inhibition of Metallo-β-Lactamases for the Treatment of Carbapenem-Resistant Gram-Negative Bacterial Infections.

Vitaly G Grigorenko, Maria G Khrenova, Irina P Andreeva, Maya Yu Rubtsova, Anastasia I Lev, Tatiana S Novikova, Elena V Detusheva, Nadezhda K Fursova, Ivan A Dyatlov, Alexey M Egorov

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 15 citations in OpenAlex.

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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

10 authors at 3 institutions in 1 country.

Vitaly G GrigorenkoDepartment of Chemistry, Lomonosov Moscow State University, 119991 Moscow, Russia.ORCID 0000-0003-0352-4902
Maria G KhrenovaDepartment of Chemistry, Lomonosov Moscow State University, 119991 Moscow, Russia.ORCID 0000-0001-7117-3089
Irina P AndreevaDepartment of Chemistry, Lomonosov Moscow State University, 119991 Moscow, Russia.
Maya Yu RubtsovaDepartment of Chemistry, Lomonosov Moscow State University, 119991 Moscow, Russia.ORCID 0000-0003-4025-5967
Anastasia I LevState Research Center for Applied Microbiology & Biotechnology, 142279 Obolensk, Russia.
Tatiana S NovikovaState Research Center for Applied Microbiology & Biotechnology, 142279 Obolensk, Russia.
Elena V DetushevaState Research Center for Applied Microbiology & Biotechnology, 142279 Obolensk, Russia.
Nadezhda K FursovaState Research Center for Applied Microbiology & Biotechnology, 142279 Obolensk, Russia.ORCID 0000-0001-6053-2621
Ivan A DyatlovState Research Center for Applied Microbiology & Biotechnology, 142279 Obolensk, Russia.
Alexey M EgorovDepartment of Chemistry, Lomonosov Moscow State University, 119991 Moscow, Russia.
State Research Center for Applied Microbiology and Biotechnology · RULomonosov Moscow State University · RURussian Academy of Sciences · RU

Funding

Lomonosov Moscow State University state task АААА-А21- 121011290089-4Ministry of Science and Higher Education of the Russian Federation 075-15-2019- 1671Russian Science Foundation 18-74-10056
6 · The paper itself

Abstract

The increasing antibiotic resistance is a clinical problem worldwide. Numerous Gram-negative bacteria have already become resistant to the most widely used class of antibacterial drugs, β-lactams. One of the main mechanisms is inactivation of β-lactam antibiotics by bacterial β-lactamases. Appearance and spread of these enzymes represent a continuous challenge for the clinical treatment of infections and for the design of new antibiotics and inhibitors. Drug repurposing is a prospective approach for finding new targets for drugs already approved for use. We describe here the inhibitory potency of known detoxifying antidote 2,3-dimercaptopropane-1-sulfonate (unithiol) against metallo-β-lactamases. Unithiol acts as a competitive inhibitor of meropenem hydrolysis by recombinant metallo-β-lactamase NDM-1 with the K

Indexed as

beta-Lactamase Inhibitorsbeta-LactamasesCarbapenemsDrug RepositioningDrug Resistance, BacterialGene Expression Regulation, BacterialGene Expression Regulation, EnzymologicKlebsiella pneumoniaeModels, MolecularProtein ConformationPseudomonas aeruginosaQuantitative Structure-Activity RelationshipUnithiolbeta-Lactamase Inhibitorsbeta-lactamase NDM-1beta-LactamasesCarbapenemsUnithiolVIM-1 metallo-beta-lactamaseantibiotic resistancedrug repurposingmetallo-β-lactamasemolecular modeling

Identifiers

PMID35163756
PMCPMC8837113
OpenAlexW4210794212

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.