Evidence map›Paper›PMID 42127270›Full record

ArticleChemistry & biodiversity2026

Antibacterial and Antibiofilm Efficacy of 2-Phenyl Ethyl Methyl Ether Against Multidrug-Resistant Klebsiella pneumoniae.

Monika Mishra, Subhaswaraj Pattnaik, Pratyush Pragyandipta, Eeshara Naik, Dibyadarshini Sahu, Aparajita Priyadarshini, Pradeep Kumar Naik

Abstract read
In one paragraph

Article in Chemistry & biodiversity, 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

7 authors.

Monika MishraCentre of Excellence in Natural Products and Therapeutics, Department of Biotechnology and Bioinformatics, Sambalpur University, Sambalpur, Odisha, India.
Subhaswaraj PattnaikCentre of Excellence in Natural Products and Therapeutics, Department of Biotechnology and Bioinformatics, Sambalpur University, Sambalpur, Odisha, India.
Pratyush PragyandiptaCentre of Excellence in Natural Products and Therapeutics, Department of Biotechnology and Bioinformatics, Sambalpur University, Sambalpur, Odisha, India.
Eeshara NaikCentre of Excellence in Natural Products and Therapeutics, Department of Biotechnology and Bioinformatics, Sambalpur University, Sambalpur, Odisha, India.
Dibyadarshini SahuCentre of Excellence in Natural Products and Therapeutics, Department of Biotechnology and Bioinformatics, Sambalpur University, Sambalpur, Odisha, India.
Aparajita PriyadarshiniDepartment of Food Science Technology and Nutrition, Sambalpur University, Sambalpur, Odisha, India.
Pradeep Kumar NaikCentre of Excellence in Natural Products and Therapeutics, Department of Biotechnology and Bioinformatics, Sambalpur University, Sambalpur, Odisha, India.ORCID https://orcid.org/0000-0001-7044-2427

Funding

CSIR, IndiaDBT-BUILDER BT/INF/22/SP45357/2022
6 · The paper itself

Abstract

The rise of Klebsiella pneumoniae (Kp) as an MDR pathogen has become a pressing global health challenge, contributing to UTIs and Pneumonia. A major factor underlying its persistence and antibiotic resistance is its inherent ability to form protective biofilm matrices. This study explores a natural approach to combat Kp biofilms by leveraging the antibacterial potential of plant-derived essential oils. Among bioactive compounds, 2-Phenyl ethyl methyl ether, a constituent of kewda oil, appears as a viable option. Our investigation revealed that 2-PEME exhibits significant antibacterial activity against Kp with a MIC of 50 mM, and the clinical isolate was further confirmed by morphological and molecular characterization. Notably, at a sub-MIC concentration of 25 mM, 2-PEME disrupted biofilm formation, reducing biofilm biomass by 61.17% ± 3.75% and 59.30% ± 6.24% in Kp and MTCC-109, respectively. These findings were further corroborated through microscopic analysis, providing strong evidence of 2-PEME's biofilm-inhibiting potential. To elucidate the mechanism of action, molecular docking studies were performed, which predicted strong binding affinities between 2-PEME and key biofilm-associated and drug-resistant proteins in Kp. Cell viability assays conducted on HEK-293, 3T3L1, and L929 cell lines demonstrated no cytotoxic effects, confirming their viability as a safe alternative. Computational pharmacokinetic analysis further supported its drug-like properties.

Indexed as

Anti-Bacterial AgentsBiofilmsDrug Resistance, Multiple, BacterialKlebsiella pneumoniaePhenyl EthersAnimalsCell SurvivalDose-Response Relationship, DrugHumansMiceMicrobial Sensitivity TestsMolecular Docking SimulationStructure-Activity RelationshipAnti-Bacterial AgentsPhenyl Ethers2‐Phenyl ethyl methyl etherantibacterialbiofilmKlebsiella pneumoniaeMICmolecular dockingMTT

Identifiers

PMID42127270
PMCPMC13381008

What OpenQuestion holds

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Registered trials

None linked

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.