Evidence map›Paper›PMID 42673313›Full record

ArticleChembiochem : a European journal of chemical biology2026

Benzylamine-Based Organoselenium Compounds as Glutathione Peroxidase Mimics: Antioxidant and Antibacterial Agents.

Nikhil Sodhi, Rajni Kadian, Aboobacker P A, Thiyagarajan Sanjeevi, Vijay P Singh

Abstract read
In one paragraph

Article in Chembiochem : a European journal of chemical biology, 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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0citing papers 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

The trial behind it

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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

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5 · Who and what money

Authors and funding

5 authors.

Nikhil SodhiDepartment of Chemistry & Centre of Advanced Studies in Chemistry, Panjab University, Chandigarh, India.ORCID https://orcid.org/0000-0002-9611-1375
Rajni KadianDepartment of Chemistry & Centre of Advanced Studies in Chemistry, Panjab University, Chandigarh, India.
Aboobacker P ADepartment of Microbiology, Aarupadai Veedu Medical College and Hospital, Vinayaka Mission's Research Foundation (DU), Puducherry, India.ORCID https://orcid.org/0000-0002-2066-597X
Thiyagarajan SanjeeviDepartment of Medical Biotechnology, Aarupadai Veedu Medical College and Hospital, Vinayaka Mission's Research Foundation (DU), Puducherry, India.ORCID https://orcid.org/0000-0002-4006-7184
Vijay P SinghDepartment of Chemistry & Centre of Advanced Studies in Chemistry, Panjab University, Chandigarh, India.ORCID https://orcid.org/0000-0002-5584-2067

Funding

Anusandhan National Research Foundation SUR/2022/002214
6 · The paper itself

Abstract

Benzylamine-based organoselenium compounds were designed and synthesized to explore their antioxidant and antibacterial properties. The synthetic strategy involves nucleophilic substitution of benzyl bromides with in situ generated sodium selenolate, obtained from sodium borohydride reduction of the corresponding diselenides, affording the desired products. The multifunctional antioxidant properties, including radical-trapping and glutathione peroxidase-like antioxidant activities were evaluated using 2,2-diphenyl-1-picrylhydrazyl and thiophenol assay, respectively. These antioxidants exhibited good cell viability at 2 µM and displayed in vitro antibacterial activity against gram-negative Escherichia coli and gram-positive Staphylococcus aureus. These were further supported by in silico study.

Indexed as

Anti-Bacterial AgentsAntioxidantsBenzylaminesBiomimetic MaterialsGlutathione PeroxidaseOrganoselenium CompoundsEscherichia coliMicrobial Sensitivity TestsStaphylococcus aureusAnti-Bacterial AgentsAntioxidantsbenzylamineBenzylaminesGlutathione PeroxidaseOrganoselenium CompoundsantibacterialantioxidantbenzylamineGPx mimicsradicalselenium

Identifiers

PMID42673313
PMCPMC13529230

What OpenQuestion holds

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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.