Evidence map›Paper›PMID 42353691›Full record

ArticleAntibiotics (Basel, Switzerland)2026

Integrated In Vitro and In Silico Evaluation of Benzimidazolium Salts: Antioxidant Activity, Anti-MRSA/MSSA Effects, and Antibacterial Gene Expression Analysis.

Başak Bedir, Hakan Ünver, Mehmet Çimentepe, Özge Öztürk Çimentepe, Akın Yiğin, Metin Yildirim

Abstract read
In one paragraph

Article in Antibiotics (Basel, Switzerland), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Başak BedirDepartment of Nutrition and Dietetics, Faculty of Health Sciences, Hakkari University, Hakkâri 30000, Türkiye.ORCID 0000-0003-2207-6631
Hakan ÜnverDepartment of Chemistry, Faculty of Science, Eskisehir Technical University, Eskisehir 26555, Türkiye.
Mehmet ÇimentepeDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy, Harran University, Sanliurfa 63300, Türkiye.
Özge Öztürk ÇimentepeDepartment of Pharmacology, Faculty of Pharmacy, Harran University, Sanliurfa 63300, Türkiye.
Akın YiğinDepartment of Genetics, Faculty of Veterinary Medicine, Harran University, Sanliurfa 63200, Türkiye.
Metin YildirimDepartment of Biochemistry, Faculty of Pharmacy, Cukurova University, Adana 01330, Türkiye.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesThe emergence of methicillin-resistant

methodsFive benzimidazolium salts bearing different substituents were synthesized and characterized by NMR and FTIR analyses. Their antibacterial activities against MRSA and MSSA were investigated using the resazurin-based minimum inhibitory concentration (MIC) assay and agar diffusion method. Antibiofilm activity was evaluated using crystal violet staining, while scanning electron microscopy (SEM) was employed to examine bacterial morphological changes. Gene expression analysis was performed to assess the effects of the most active compound on virulence- and resistance-related genes. In addition, molecular docking studies were conducted against four target proteins (1MWT, 3ZG5, 1JIJ, and 2Y2M).

resultsAmong the synthesized compounds, compound 1c exhibited the strongest antibacterial activity, with MIC values of 0.25 µg/mL against MRSA and 0.5 µg/mL against MSSA. It also produced the largest inhibition zone diameter (31.0 ± 0.5 mm). SEM analysis revealed significant morphological alterations in treated bacterial cells, indicating disruption of cellular integrity. Gene expression studies demonstrated that compound 1c downregulated several virulence- and resistance-associated genes, including

conclusionsThe findings demonstrate that benzimidazolium derivatives, particularly compound 1c, possess potent antibacterial and antibiofilm activities against

Indexed as

antibacterial activitybenzimidazolium derivativesgene expressionmolecular dockingMRSA

Identifiers

PMID42353691
PMCPMC13296230

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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.