Synthesis and characterization of 2,3-diaminophenazine@CuhNFs and 2,3-diaminopyridine@CuhNFs: a new strategy to enhance anticancer activity

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In this study, synthesis and characterization of 2,3-diaminophenazine@CuhNFs and 2,3-diaminopyridine@CuhNFs were carried out. The morphologies of the synthesized CuhNFs were investigated using Fourier Transform Infrared spectrometry, scanning electron microscopy and energy dispersive X-ray, elemental mapping, and XRD spectroscopy. Organic compounds and synthesized nanoflowers were screened against human lung (A549) and breast (MCF-7) cancer cell lines. The results show that the tested compounds had cytotoxic activity in both cell lines. To support the in vitro part of the study, the MTT results were also examined by in silico approaches. The binding parameter values of compounds interacting via in silico with 1M17 and 3ERT crystal structures in molecular docking and important amino acids in the binding site were determined. The pharmacokinetic properties and toxicity of compounds were evaluated using ADMET analysis. © 2026 Taylor & Francis Group, LLC.

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dc.contributor.authorSomturk-Yilmaz, Burcu
dc.contributor.authorTurkmenoglu, Burçin
dc.contributor.authorAkkoc, Senem
dc.date.accessioned2026-10-18T20:25:41.241998106Z
dc.date.available2026-10-18T20:25:41.241998106Z
dc.date.issued2026
dc.description.abstractIn this study, synthesis and characterization of 2,3-diaminophenazine@CuhNFs and 2,3-diaminopyridine@CuhNFs were carried out. The morphologies of the synthesized CuhNFs were investigated using Fourier Transform Infrared spectrometry, scanning electron microscopy and energy dispersive X-ray, elemental mapping, and XRD spectroscopy. Organic compounds and synthesized nanoflowers were screened against human lung (A549) and breast (MCF-7) cancer cell lines. The results show that the tested compounds had cytotoxic activity in both cell lines. To support the in vitro part of the study, the MTT results were also examined by in silico approaches. The binding parameter values of compounds interacting via in silico with 1M17 and 3ERT crystal structures in molecular docking and important amino acids in the binding site were determined. The pharmacokinetic properties and toxicity of compounds were evaluated using ADMET analysis. © 2026 Taylor & Francis Group, LLC.
dc.description.sponsorshipThe authors thank Erzincan Binali Y\u0131ld\u0131r\u0131m University, Basic Sciences Application and Research Center (EBYU-EUTAM) for the usage of the Schr\u00F6dinger Maestro 2021-2 program. S. Akkoc thanks the Suleyman Demirel University Research Fund (TSG-2024-9516) for financial support.
dc.identifier.doi10.1080/24701556.2026.2667229
dc.identifier.eissn2470-1564
dc.identifier.endpage573
dc.identifier.issn2470-1556
dc.identifier.issue6
dc.identifier.scopus2-s2.0-105038700966
dc.identifier.startpage561
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/10473
dc.identifier.volume56
dc.identifier.wosWOS:001764382500001
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofInorganic and Nano-Metal Chemistry
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAnticancer
dc.subjecthybrid
dc.subjectmolecular docking
dc.subjectnanoflower
dc.subjectphenazine
dc.subjectpyridine
dc.titleSynthesis and characterization of 2,3-diaminophenazine@CuhNFs and 2,3-diaminopyridine@CuhNFs: a new strategy to enhance anticancer activity
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus0
rdl.citation.wos0
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)