Evidence map›Paper›PMID 41712543›Full record

ArticleChemMedChem2026

Cytotoxicity and Antimicrobial Activity of GaMF1 Analogs.

Jan Chasák, Petr Vyvlečka, Ivan Nemec, An Matheeussen, Natascha Van Pelt, Paul Cos, Guy Caljon, Vladimír Kryštof, Lucie Brulíková

Abstract read
In one paragraph

Article in ChemMedChem, 2026. 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

9 authors.

Jan ChasákDepartment of Organic Chemistry, Faculty of Science, Palacký University Olomouc, Olomouc, Czech Republic.
Petr VyvlečkaDepartment of Organic Chemistry, Faculty of Science, Palacký University Olomouc, Olomouc, Czech Republic.
Ivan NemecDepartment of Inorganic Chemistry, Faculty of Science, Palacký University Olomouc, Olomouc, Czech Republic.
An MatheeussenLaboratory of Microbiology, Parasitology and Hygiene (LMPH), Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, Infla-Med Centre of Excellence, University of Antwerp, Wilrijk, Belgium.
Natascha Van PeltLaboratory of Microbiology, Parasitology and Hygiene (LMPH), Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, Infla-Med Centre of Excellence, University of Antwerp, Wilrijk, Belgium.
Paul CosLaboratory of Microbiology, Parasitology and Hygiene (LMPH), Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, Infla-Med Centre of Excellence, University of Antwerp, Wilrijk, Belgium.
Guy CaljonLaboratory of Microbiology, Parasitology and Hygiene (LMPH), Faculty of Pharmaceutical, Biomedical and Veterinary Sciences, Infla-Med Centre of Excellence, University of Antwerp, Wilrijk, Belgium.
Vladimír KryštofDepartment of Experimental Biology, Faculty of Science, Palacký University Olomouc, Olomouc, Czech Republic.
Lucie BrulíkováDepartment of Organic Chemistry, Faculty of Science, Palacký University Olomouc, Olomouc, Czech Republic.ORCID https://orcid.org/0000-0001-8380-073X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have identified the mycobacterial adenosine triphosphate synthase inhibitor GaMF1 and its structural analogs as compounds with noteworthy antituberculosis activity. Despite these promising results, a significant limitation remains their cytotoxicity against human cells, which, in its current state, overshadows the therapeutic potential. Therefore, addressing this off-target toxicity is essential for the further development of these compounds as viable drug candidates. In this study, we systematically explored structural modifications of the original GaMF1 scaffold with the primary aim of reducing its inherent cytotoxicity. Individual regions of the parent structure were progressively replaced, enabling the identification of substituents that effectively attenuate cytotoxic effects. Importantly, these structural refinements also led to the emergence of pronounced antiparasitic activity, particularly against trypanosomal species such as Trypanosoma cruzi, Trypanosoma brucei brucei, and Trypanosoma brucei rhodesiense. These findings suggest that the biological potential of this compound class extends beyond what has previously been described. Furthermore, we evaluated the cytotoxicity of selected derivatives against a panel of tumor cell lines, where some compounds showed encouraging antiproliferative effects.

Indexed as

AminopyridinesAntineoplastic AgentsTrypanocidal AgentsCell Line, TumorCell ProliferationDose-Response Relationship, DrugDrug Screening Assays, AntitumorHumansMicrobial Sensitivity TestsMolecular StructureParasitic Sensitivity TestsStructure-Activity RelationshipTrypanosoma brucei bruceiTrypanosoma brucei rhodesienseTrypanosoma cruziAminopyridinesAntineoplastic AgentsTrypanocidal Agents2,4‐diaminopyridineantiparasiticantiproliferativeantituberculosiscytotoxicityGaMF1trypanosomes

Identifiers

PMID41712543
PMCPMC12919900

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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.