Evidence map›Paper›PMID 39835639›Full record

ArticleChemical biology & drug design2025

Antimicrobial and Antiproliferative Properties of 2-Phenyl-N-(Pyridin-2-yl)acetamides.

Daria Nawrot, Barbora Koutníková, Ondřej Janďourek, Klára Konečná, Martin Novák, Pavla Paterová, Pavel Bárta, Ghada Bouz, Jan Zitko, Martin Doležal

Abstract read
In one paragraph

Article in Chemical biology & drug design, 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

10 authors.

Daria NawrotFaculty of Pharmacy in Hradec Králové, Charles University, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0002-8858-1529
Barbora KoutníkováFaculty of Pharmacy in Hradec Králové, Charles University, Hradec Králové, Czech Republic.
Ondřej JanďourekFaculty of Pharmacy in Hradec Králové, Charles University, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0003-4633-2062
Klára KonečnáFaculty of Pharmacy in Hradec Králové, Charles University, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0001-5670-7767
Martin NovákBiomedical Research Centre, University Hospital Hradec Kralove, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0001-9692-7641
Pavla PaterováDepartment of Clinical Microbiology, University Hospital, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0003-0192-7345
Pavel BártaFaculty of Pharmacy in Hradec Králové, Charles University, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0001-5445-5658
Ghada BouzFaculty of Pharmacy in Hradec Králové, Charles University, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0003-2024-5788
Jan ZitkoFaculty of Pharmacy in Hradec Králové, Charles University, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0003-0104-9925
Martin DoležalFaculty of Pharmacy in Hradec Králové, Charles University, Hradec Králové, Czech Republic.ORCID https://orcid.org/0000-0003-1558-6625

Funding

Ministry of Education, Youth and Sports of the Czech Republic SVV 260 666Ministry of Health of the Czech Republic NU21-05-00482
6 · The paper itself

Abstract

Infectious diseases, including bacterial, fungal, and viral, have once again gained urgency in the drug development pipeline after the recent COVID-19 pandemic. Tuberculosis (TB) is an old infectious disease for which eradication has not yet been successful. Novel agents are required to have potential activity against both drug-sensitive and drug-resistant strains of Mycobacterium tuberculosis (Mtb), the causative agent of TB. In this study, we present a series of 2-phenyl-N-(pyridin-2-yl)acetamides in an attempt to investigate their possible antimycobacterial activity, cytotoxicity on the HepG2 liver cancer cell line, and-as complementary testing-their antibacterial and antifungal properties against a panel of clinically important pathogens. This screening resulted in one compound with promising antimycobacterial activity-compound 12, MIC

Indexed as

AcetamidesCell ProliferationMicrobial Sensitivity TestsMycobacterium tuberculosisAntifungal AgentsAntineoplastic AgentsAntitubercular AgentsCell Line, TumorHep G2 CellsHumansPyridinesSARS-CoV-2Structure-Activity RelationshipAcetamidesAntifungal AgentsAntineoplastic AgentsAntitubercular AgentsPyridinesantibacterialantimycobacterialantiproliferativedrug designpyridinetuberculosis

Identifiers

PMID39835639
PMCPMC11748363

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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.