Evidence map›Paper›PMID 40325815›Full record

ArticleCurrent drug discovery technologies2026

Bioactive Compounds as a Potential Inhibitor of Biofilm Production: An

Jai Gupta, Avi Gupta, Debasmita Bhattacharya, Moupriya Nag, Dibyajit Lahiri, Debanjan Mitra

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Article in Current drug discovery technologies, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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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.

Jai GuptaDepartment of Biotechnology, Institute of Engineering and Management, Kolkata University of Engineering and Management, Kolkata, West Bengal, India.
Avi GuptaDepartment of Biotechnology, Institute of Engineering and Management, Kolkata University of Engineering and Management, Kolkata, West Bengal, India.
Debasmita BhattacharyaDepartment of Basic Science and Humanities, Institute of Engineering and Management, Kolkata University of Engineering and Management, Kolkata, West Bengal, India.
Moupriya NagDepartment of Biotechnology, Institute of Engineering and Management, Kolkata University of Engineering and Management, Kolkata, West Bengal, India.
Dibyajit LahiriDepartment of Biotechnology, Institute of Engineering and Management, Kolkata University of Engineering and Management, Kolkata, West Bengal, India.
Debanjan MitraDepartment of Microbiology, Raiganj University, Raiganj, West Bengal, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionBiofilm formation by microorganisms, specifically bacteria, threatens various fields, including biomedicine and the environment. The development of biofilms has associations with increased resistance to antimicrobial agents and immune responses; it poses a significant threat to human health. ESKAPE pathogens, a group of bacteria known for their multidrug resistance, are particularly adept at biofilm formation. This research explores strategies to combat biofilm-associated infections, with a focus on natural compounds as potential anti-biofilm agents.

methodsThe study investigates 23 natural compounds for their druglike properties in fighting against antibiotic-resistant biofilms. These compounds include flavonoids, terpenes, and alkaloids, and exhibit promising bioavailability and usage potential as ligands. Molecular docking analysis employing AutoDock Vina was used to evaluate the binding affinities of these ligands to key biofilmforming genes and membrane proteins in ESKAPE pathogens. RESULTS AND DISCUSSION: Despite a few violations of a variety of established criteria, the overall safety and efficiency of oral drug reception are maintained, emphasizing their potential for further drug development. The results show specific ligands, such as Baicalin, Apigenin, Azadirachtin, Curcumin, Hyperforin, etc., demonstrating high binding energies against biofilm-associated proteins. This approach aligns with the pursuit of sustainable alternatives to combat biofilm-related infections.

conclusionNatural compounds like Baicalin, Apigenin, Azadirachtin, Curcumin, Hyperforin not only exhibit broad-spectrum coverage but also show reduced risks of resistance development compared to synthetic antibiotics. The integration of natural compounds into multifaceted strategies considers the complexities of the biofilm matrix, bacterial diversity, and pathogen characteristics, offering a sustainable approach to address biofilm-associated infections.

Indexed as

Anti-Bacterial AgentsBiofilmsBiological ProductsAlkaloidsBacteriaComputer SimulationFlavonoidsHumansLigandsMolecular Docking SimulationTerpenesAlkaloidsAnti-Bacterial AgentsBiological ProductsFlavonoidsLigandsTerpenesantimicrobial agentsBiofilmESKAPE pathogengenetic driftsmolecular dockingsustainable alternatives

Identifiers

PMID40325815

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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.