Novel tetracyclic spermine derivatives of cyclotriphosphazene: Design, synthesis and biological activity

dc.contributor.authorCiftci, Gonul Yenilmez
dc.contributor.authorKilic, Sumeyra Yoldas
dc.contributor.authorYüksel, Fatma
dc.contributor.authorTurhal, Gulseren
dc.contributor.authorDemiroğlu-Zergeroğlu, Asuman
dc.date.accessioned2025-10-29T11:24:12Z
dc.date.issued2022
dc.departmentFakülteler, Temel Bilimler Fakültesi, Moleküler Biyoloji ve Genetik Bölümü
dc.departmentFakülteler, Temel Bilimler Fakültesi, Kimya Bölümü
dc.description.abstractLung cancer is amongst the deadliest form of cancer that categorized in two main groups as small cell lung cancer (SCLC) and non-small cell lung cancer (NSCLC), which arises more often and typically grows at a slower rate than SCLC. Treatment limitations due to the side effects and resistance to the current therapeutics' mandates development of alternative agents. In this study, novel tetracyclic spermine derivatives of cyclotriphosphazene (6-8) were designed and synthesized and their effects were investigated in NSCLC cell lines and non-tumoral counterparts. First, the reactions of dispiroansa (tetracyclic) spermine substituted cyclotriphosphazene derivative (2) with pyrrolidine (3), piperidine (4) and cyclopropylmethanamine (5) were performed, respectively and synthesised products (6-8) were characterized by FT-IR, MALDI-TOF MS, H-1, P-31 NMR spectroscopies and single crystal X-ray (for compound 7) crystallography. Then, the anti-carcinogenic properties of compounds have been determined by viability and cell death assays. Our results indicated that compared to others, compound 8 that is formed by the substitution reaction of compounds 2 and 5 has a potential anti-cancerogenic effect on lung cancer cells. (C) 2022 Elsevier B.V. All rights reserved.
dc.description.sponsorshipGebze Institute of Technology Research Fund
dc.description.sponsorshipThe authors would like to thank the Gebze Institute of Technology Research Fund for partial support.
dc.identifier.doi10.1016/j.molstruc.2022.132371
dc.identifier.issn0022-2860
dc.identifier.issn1872-8014
dc.identifier.orcid0009-0000-6970-723X
dc.identifier.scopus2-s2.0-85122923938
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1016/j.molstruc.2022.132371
dc.identifier.urihttps://hdl.handle.net/20.500.14854/9829
dc.identifier.volume1254
dc.identifier.wosWOS:000798687100003
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherElsevier
dc.relation.ispartofJournal of Molecular Structure
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20251020
dc.subjectCyclotriphosphazene
dc.subjectNMR
dc.subjectCytotoxicity
dc.subjectNSCLC
dc.subjectCancer
dc.titleNovel tetracyclic spermine derivatives of cyclotriphosphazene: Design, synthesis and biological activity
dc.typeArticle

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