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dc.contributor.authorBeynek, Nesrin
dc.contributor.authorUluçam, Gühergül
dc.contributor.authorBenkli, Kadriye
dc.contributor.authorKoparal, Ayşe Tansu
dc.date.accessioned2019-10-19T16:02:33Z
dc.date.available2019-10-19T16:02:33Z
dc.date.issued2008
dc.identifier.issn0018019X
dc.identifier.urihttps://dx.doi.org/10.1002/hlca.200890223
dc.identifier.urihttps://hdl.handle.net/11421/13790
dc.description.abstractIn the present work, we describe the synthesis and characterization of five new versatile acyclic or macrocyclic ligands containing binaphthyl-linked pyridine, bipyridine, or phenanthroline groups in their framework (see Schemes 1-4). The structures of the ligands were elucidated on the basis of elemental analyses, IR, 1H-NMR, 13C-NMR, and FAB mass spectra. The cytotoxicity of these compounds was tested in vitro by using the tetrazolium salt reduction (MTT) assay on A549 (human lung carcinoma epithelial like) cells. All of the tested compounds induced time- and concentration-dependent cytotoxic effecten_US
dc.language.isoengen_US
dc.relation.isversionof10.1002/hlca.200890223en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleSynthesis and characterization of new binaphthyl-linked phenanthroline-, bipyridine-, or pyridine-derived ligands, and the study of their cytotoxic activityen_US
dc.typearticleen_US
dc.relation.journalHelvetica Chimica Actaen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Farmasötik Kimya Anabilim Dalıen_US
dc.identifier.volume91en_US
dc.identifier.issue11en_US
dc.identifier.startpage2089en_US
dc.identifier.endpage2096en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US]
dc.contributor.institutionauthorBenkli, Kadriye
dc.contributor.institutionauthorKoparal, Ayşe Tansu


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