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dc.contributor.authorYurttaş, Leyla
dc.contributor.authorErtaş, Merve
dc.contributor.authorÇiftçi, Gülsen Akalın
dc.contributor.authorTemel, Halide Edip
dc.contributor.authorDemirayak, Şeref
dc.date.accessioned2019-10-19T16:02:34Z
dc.date.available2019-10-19T16:02:34Z
dc.date.issued2017
dc.identifier.issn1307-2080
dc.identifier.urihttps://dx.doi.org/10.23893/1307-2080.APS.0553
dc.identifier.urihttps://hdl.handle.net/11421/13805
dc.description.abstractIn this work, some novel N-(6-substituted-benzothiazol-2-yl)-2-[[4,5-dimethyl-1-((p-tolyl/4-nitrophenyl)amino)-1H-imidazol-2-yl]thio]acetamide derivatives were synthesized and searched for their cytotoxic activities against C6 and HepG2 tumor cells. Among all compounds, the most active compound was determined as compound 7. It was calculated IC50 value about 15.67 µg/mL through C6 tumor cell lines and also compound 2, 4, 5, 6 were observed as good cytotoxic agents against HepG2 tumor cells. Findings about antiproliferative activity studies have encouraged the acquirement of new similar compounds in undergoing studiesen_US
dc.language.isoengen_US
dc.publisherUniversity of Istanbulen_US
dc.relation.isversionof10.23893/1307-2080.APS.0553en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectAntiproliferative Activityen_US
dc.subjectBenzothiazoleen_US
dc.subjectCytotoxicityen_US
dc.subjectImidazoleen_US
dc.titleNovel benzothiazole based imidazole derivatives as new cytotoxic agents against glioma (C6) and liver (HepG2) cancer cell linesen_US
dc.typearticleen_US
dc.relation.journalActa Pharmaceutica Scienciaen_US
dc.contributor.departmentAnadolu Üniversitesi, Eczacılık Fakültesi, Farmasötik Kimya Anabilim Dalıen_US
dc.identifier.volume55en_US
dc.identifier.issue1en_US
dc.identifier.startpage39en_US
dc.identifier.endpage47en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US]
dc.contributor.institutionauthorYurttaş, Leyla
dc.contributor.institutionauthorÇiftçi, Gülsen Akalın
dc.contributor.institutionauthorTemel, Halide Edip
dc.contributor.institutionauthorDemirayak, Şeref


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