New cyclometalated iridium(III) complexes bearing substituted 2-(1H-benzimidazol-2-yl)quinoline: Synthesis, characterization, electrochemical and anticancer studies

dc.authorid0000-0001-6982-9536
dc.authorid0000-0003-3259-5822
dc.contributor.authorSahin, Cigdem
dc.contributor.authorMutlu, Dogukan
dc.contributor.authorErdem, Ahmet
dc.contributor.authorKilincarslan, Rafet
dc.contributor.authorArslan, Sevki
dc.date.accessioned2025-05-10T19:48:45Z
dc.date.issued2024
dc.departmentİstanbul Medeniyet Üniversitesi
dc.description.abstractNew iridium(III) compounds (C1-C3) bearing 2-(1H-benzimidazol-2-yl)quinoline ligands with different side groups (benzyl, 2,3,4,5,6-pentamethylbenzyl and 2,3,4,5,6-pentafluorobenzyl) were synthesized and characterized by using spectroscopic analyses. The effects of different side groups of iridium compounds on the photophysical and electrochemical properties have been investigated. The cytotoxicity and apoptosis of the compounds have been evaluated on breast cancer cell lines using various methods including MTT assay, flow cytometry, qRT-PCR, and colony formation. The cytotoxicity of C1, expressed as IC50 values, was found to be 11.76 mu M for MDA-MB-231 and 5.35 mu M for MCF-7 cells. For C3, the IC50 value was 16.22 mu M for MDA-MB-231 and 8.85 mu M for MCF-7 cells. In both cell lines, increased levels of Bax and caspase 3, along with downregulation of BCL-2 and positive annexin V staining, were observed, confirming apoptosis. Moreover, the colony-forming abilities in both cell lines decreased after C1 and C3 complex treatment. All these results suggest that the compounds C1 and C3 may have potential in the treatment of breast cancer, though further research is needed to confirm their efficacy.
dc.description.sponsorshipResearch Fund of Istanbul Medeniyet University [GAP-2022-1813]; Pamukkale University Scientific Research Projects Commission [2014FEBE035, 2016FEBE013, 2017FEBE042]
dc.description.sponsorshipThe synthesis and anticancer studies of the iridium complexes bearing 2-(1H-benzimidazol-2-yl) quinoline have been supported by Research Fund of Istanbul Medeniyet University (Project Number: GAP-2022-1813). The synthesis of 2-(1H-benzimidazol-2-yl) quinoline ligands part of this paper has been supported by Pamukkale University Scientific Research Projects Commission (Project No: 2014FEBE035, 2016FEBE013 and 2017FEBE042).
dc.identifier.doi10.1016/j.bioorg.2024.107706
dc.identifier.issn0045-2068
dc.identifier.issn1090-2120
dc.identifier.pmid39128244
dc.identifier.scopus2-s2.0-85200848281
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1016/j.bioorg.2024.107706
dc.identifier.urihttps://hdl.handle.net/20.500.14730/11786
dc.identifier.volume151
dc.identifier.wosWOS:001294449300001
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoen
dc.publisherAcademic Press Inc Elsevier Science
dc.relation.ispartofBioorganic Chemistry
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250302
dc.subjectIridium complex
dc.subject2-(1H-benzimidazol-2-yl)quinoline
dc.subjectCytotoxicity
dc.subjectApoptosis
dc.titleNew cyclometalated iridium(III) complexes bearing substituted 2-(1H-benzimidazol-2-yl)quinoline: Synthesis, characterization, electrochemical and anticancer studies
dc.typeArticle

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