Evidence map›Paper›PMID 40056185›Full record

ArticleJournal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry2025

Bismuth(III) complexes of Schiff bases derived from aliphatic amines: interaction with biomolecules and antimicrobial activity.

Maxim Gvozdev, Iveta Turomsha, Nikolai Osipovich, Galina Ksendzova, Alina Khodosovskaya, Anton Siomchen, Janusz M Dąbrowski, Natalia Loginova

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Article in Journal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry, 2025. 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

8 authors.

Maxim GvozdevFaculty of Chemistry, Belarusian State University, 4 Independence Avenue, 220030, Minsk, Belarus.ORCID 0000-0002-4504-2090
Iveta TuromshaFaculty of Chemistry, Belarusian State University, 4 Independence Avenue, 220030, Minsk, Belarus.ORCID 0000-0003-0833-9271
Nikolai OsipovichResearch Institute for Physico-Chemical Problems of the Belarusian State University, Leningradskaya Str. 14, 220030, Minsk, Belarus.ORCID 0000-0001-6354-5292
Galina KsendzovaResearch Institute for Physico-Chemical Problems of the Belarusian State University, Leningradskaya Str. 14, 220030, Minsk, Belarus.ORCID 0000-0001-7121-0249
Alina KhodosovskayaFaculty of Biology, Belarusian State University, 4 Independence Avenue, 220030, Minsk, Belarus.ORCID 0000-0002-4987-7079
Anton SiomchenFaculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387, Kraków, Poland.ORCID 0009-0007-6598-2446
Janusz M DąbrowskiFaculty of Chemistry, Jagiellonian University, Gronostajowa 2, 30-387, Kraków, Poland.ORCID 0000-0002-8791-7035
Natalia LoginovaFaculty of Chemistry, Belarusian State University, 4 Independence Avenue, 220030, Minsk, Belarus. loginonv@gmail.com.ORCID 0000-0003-0531-3594

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schiff bases bearing a sterically hindered phenolic moiety and their Bi(III) complexes were synthesized and characterized by physicochemical, quantum chemical, and biological methods. The compounds were screened in vitro against bacterial and yeast strains. It was found that Bi(III) complexes demonstrate higher antimicrobial activity compared to the parent ligands as well as to the commonly used drug (De-Nol®). Moreover, the antibacterial activity of investigated compounds did not directly correlate with their hemolytic activity, indicating that the antimicrobial effect of Bi(III) complexes cannot be explained solely by their membranolytic properties. Spectrofluorometric studies of the interaction of the Bi(III) complexes with plasma proteins indicate their moderate to high affinity toward BSA and hemoglobin, which is crucial for the determination of their pharmacological profile as well as toxicity assessment. Additionally, molecular docking was performed to predict the possible interaction modes and binding energies of the tested compounds at the molecular level. The results obtained may provide the basis for the design and development of novel Bi(III)-based antimicrobial agents.

Indexed as

AminesAnti-Bacterial AgentsAntifungal AgentsAnti-Infective AgentsBismuthCoordination ComplexesAnimalsCattleHumansMicrobial Sensitivity TestsMolecular Docking SimulationMolecular StructureSchiff BasesSerum Albumin, BovineAminesAnti-Bacterial AgentsAntifungal AgentsAnti-Infective AgentsBismuthCoordination ComplexesSchiff BasesSerum Albumin, BovineBismuth complexesCyclic voltammetryDFT calculationsMolecular dockingProtein bindingSchiff bases

Identifiers

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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.