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dc.contributor.authorYildirim, Tuba
dc.contributor.authorBilgin, Kemal
dc.contributor.authorCiftci, Gonul Yenilmez
dc.contributor.authorEcik, Esra Tanriverdi
dc.contributor.authorSenkuytu, Elif
dc.contributor.authorUludag, Yildiz
dc.contributor.authorTomak, Leman
dc.contributor.authorKilic, Adem
dc.date.accessioned2019-09-01T13:06:50Z
dc.date.available2019-09-01T13:06:50Z
dc.date.issued2012
dc.identifier.issn0223-5234
dc.identifier.urihttps://dx.doi.org/10.1016/j.ejmech.2012.03.018
dc.identifier.urihttps://hdl.handle.net/20.500.12450/1550
dc.descriptionWOS: 000304291600020en_US
dc.descriptionPubMed ID: 22483088en_US
dc.description.abstractIn the present study, a number of new dispirobino and dispiroansa spermine derivatives of cyclotriphosphazene (8-10, 13) were synthesized and characterized by elemental analysis, mass spectrometry, H-1 and P-31 NMR spectroscopy. At first, in vitro cytotoxic activity of cyclotriphosphazene compounds (1-14) against HT-29 (human colon adenocarcinoma), Hep2 (Human epidermoid larynx carcinoma), and Vero (African green monkey kidney) cell lines was investigated. Our study showed that most of these compounds stimulate apoptosis and they have cytotoxic effects for HT-29 and Hep2 cells. Additionally, these compounds (1-14) were investigated for their antibacterial activity against gram-positive (Staphylococcus aureus), gram-negative (Escherichia coli, Pseudomonas aeruginosa) bacteria and for their antifungal activity against Candida albicans, and were shown to be inactive. (C) 2012 Elsevier Masson SAS. All rights reserved.en_US
dc.description.sponsorshipScientific and Technical Research Council of Turkey TUBITAK [108T355]en_US
dc.description.sponsorshipThe authors thank the Scientific and Technical Research Council of Turkey for financial support TUBITAK (Grant 108T355). We are grateful to Dilek USTA for technical assistance for use of the flow cytometer at the Department of Hematology, Ondokuz Mayis University Hospital, Samsun.en_US
dc.language.isoengen_US
dc.publisherELSEVIER FRANCE-EDITIONS SCIENTIFIQUES MEDICALES ELSEVIERen_US
dc.relation.isversionof10.1016/j.ejmech.2012.03.018en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCyclotriphosphazeneen_US
dc.subjectSpermine derivativesen_US
dc.subjectBiological activityen_US
dc.subjectCytotoxic activityen_US
dc.subjectApoptosisen_US
dc.titleSynthesis, cytotoxicity and apoptosis of cyclotriphosphazene compounds as anti-cancer agentsen_US
dc.typearticleen_US
dc.relation.journalEUROPEAN JOURNAL OF MEDICINAL CHEMISTRYen_US
dc.authoridSenkuytu, Elif -- 0000-0002-3579-8062en_US
dc.identifier.volume52en_US
dc.identifier.startpage213en_US
dc.identifier.endpage220en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.contributor.department-temp[Yildirim, Tuba] Amasya Univ, Dept Biol, Fac Art & Sci, TR-05100 Amasya, Turkey -- [Bilgin, Kemal] Ondokuz Mayis Univ, Dept Med Microbiol, Fac Med, TR-55139 Samsun, Turkey -- [Ciftci, Gonul Yenilmez -- Ecik, Esra Tanriverdi -- Senkuytu, Elif -- Kilic, Adem] Gebze Inst Technol, Dept Chem, TR-41400 Gebze, Turkey -- [Uludag, Yildiz] UEKAE Sci & Technol Res Council Turkey TUBITAK, TR-41470 Gebze, Turkey -- [Tomak, Leman] Ondokuz Mayis Univ, Dept Biostat, Fac Med, TR-55139 Samsun, Turkeyen_US


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