Evidence map›Paper›PMID 40237183›Full record

ArticleChemMedChem2025

Novel Quinazolinones Active against Multidrug-Resistant Mycobacterium Tuberculosis: Synthesis, Antimicrobial Evaluation, and in Silico Exploration of Penicillin-Binding Protein 1A as a Potential Target.

Marek Kerda, Daria Nawrot, Petr Šlechta, Miroslav Domanský, Asal Askari, Hanieh Kamangar, Ondřej Janďourek, Klára Konečná, Pavla Paterová, Ingrid Hlbočanová and 6 more

Abstract read
In one paragraph

Article in ChemMedChem, 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

16 authors.

Marek KerdaFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0002-5850-5381
Daria NawrotFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0002-8858-1529
Petr ŠlechtaFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0002-7814-9353
Miroslav DomanskýFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.
Asal AskariFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.
Hanieh KamangarFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.
Ondřej JanďourekFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0003-4633-2062
Klára KonečnáFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0001-5670-7767
Pavla PaterováDepartment of Clinical Microbiology, University Hospital Hradec Králové, 500 05, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0003-0192-7345
Ingrid HlbočanováFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.
Miloslav MacháčekFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0001-7221-5914
Matteo MoriDepartment of Pharmaceutical Sciences, Università degli Studi di Milano, 20133, Milano, Italy.ORCID https://orcid.org/0000-0002-7491-1494
Fiorella MeneghettiDepartment of Pharmaceutical Sciences, Università degli Studi di Milano, 20133, Milano, Italy.ORCID https://orcid.org/0000-0002-6511-7360
Martin DoležalFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0003-1558-6625
Jan ZitkoFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0003-0104-9925
Ghada BouzFaculty of Pharmacy in Hradec Králové, Charles University, 500 05, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0003-2024-5788

Funding

The National Institute of Virology and Bacteriology LX22NPO5103Univerzita Karlova v Praze SVV 260 666
6 · The paper itself

Abstract

Quinazolinone derivatives have emerged as promising scaffolds in antimicrobial drug discovery. This work focuses on the design, synthesis, and evaluation of novel quinazolinone-based compounds and predicts their potential to interact with mycobacterial penicillin-binding proteins (PBPs). Relying on established structure-activity relationships of antibacterial quinazolinones, a total of 53 compounds belonging to three different structural types are synthesized and biologically evaluated for antimycobacterial, antibacterial, and antifungal activities. Biological evaluations reveal selective efficacy against Mycobacterium tuberculosis with minimum inhibitory concentrations (MICs) as low as 6.25 μg mL

Indexed as

Antifungal AgentsAntitubercular AgentsMycobacterium tuberculosisPenicillin-Binding ProteinsQuinazolinonesDose-Response Relationship, DrugDrug Resistance, Multiple, BacterialMicrobial Sensitivity TestsMolecular Docking SimulationMolecular StructureStructure-Activity RelationshipAntifungal AgentsAntitubercular AgentsPenicillin-Binding ProteinsQuinazolinonesantimycobacterialcomputational chemistriesdrug designsmedicinal chemistriesmultidrug‐resistant tuberculosispenicillin‐binding proteinsquinazolinones

Identifiers

PMID40237183
PMCPMC12221116

What OpenQuestion holds

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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.