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dc.contributor.authorYapici, Ismail
dc.contributor.authorAltay, Ahmet
dc.contributor.authorOzturk Sarikaya, Beyza
dc.contributor.authorKorkmaz, Mustafa
dc.contributor.authorAtila, Alptug
dc.contributor.authorGulcin, Ilhami
dc.contributor.authorKoksal, Ekrem
dc.date.accessioned2021-11-09T19:49:17Z
dc.date.available2021-11-09T19:49:17Z
dc.date.issued2021
dc.identifier.issn1612-1872
dc.identifier.issn1612-1880
dc.identifier.urihttps://doi.org/10.1002/cbdv.202000812
dc.identifier.urihttps://hdl.handle.net/20.500.12440/3998
dc.description.abstractIn this study, phenolic composition, and in vitro biological activities of ethyl acetate (EAE) and methanol (ME) extracts obtained from the aerial parts of endemic Tanacetum erzincanense were investigated. Total phenolic and flavonoid content of the extracts were determined by Folin-Ciocalteu and aluminum chloride colorimetric methods, respectively. Antioxidant capacity of the extracts was evaluated over radical scavenging (DPPH and ABTS) and metal ion reducing power (FRAP and CUPRAC) tests. Individual phenolic compounds in ME was analyzed by high-performance liquid chromatography coupled to electrospray ionization quadrupole time-of-flight mass spectrometry (LC-ESI-QTOF/MS). Cell inhibitory potential of the extracts was tested against colorectal adenocarcinoma (HT-29), breast adenocarcinoma (MCF-7), and hepatocarcinoma (HepG2) cells by 2,3-bis(2-methoxy-4-nitro-5-sulfophenyl)-2H-tetrazolium-5-carboxanilide (XTT) assay. The results showed that ME contains higher TPC (64.4 mg GAE/g) and TFC (62.2 mg QE/g) than those of EAE (41.5 mg GAE/g and 40.0 mg QE/g). LC-ESI-QTOF/MS analysis revealed that ME is rich in phenolic compounds, namely, chlorogenic acid, apigenin, quercetin, luteolin, and diosmetin. Antioxidant assay results indicated that ME possess stronger activity than EAE and a power that competes with synthetic antioxidants. XTT assay results demonstrated that although both extracts displayed a considerable cytotoxicity against the tested cancer cell lines in a time and dose-dependent manner, ME expressed its selective inhibitory action towards MCF-7 cells with an IC50 value of 20.4 mu g/mL for 72 h. These results may serve as a basis for further in vivo studies to examine the potential applications of T. erzincanense in food and pharmaceutical industries.en_US
dc.description.sponsorshipErzincan University Scientific Research Projects Coordination Commission (EU-BAP)Erzincan Binali Yildirim University [FBA-2016-381]en_US
dc.description.sponsorshipThis work was financially supported by grants from Erzincan University Scientific Research Projects Coordination Commission (EU-BAP) (Project No. FBA-2016-381).en_US
dc.language.isoengen_US
dc.publisherWiley-V C H Verlag Gmbhen_US
dc.relation.ispartofChemistry & Biodiversityen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectTanacetum erzincanenseen_US
dc.subjectAsteraceaeen_US
dc.subjectantioxidant activityen_US
dc.subjectcytotoxicityen_US
dc.subjectpolyphenolsen_US
dc.subjectLC-ESI-QTOFen_US
dc.subjectMSen_US
dc.titleIn vitro Antioxidant and Cytotoxic Activities of Extracts of Endemic Tanacetum erzincanense Together with Phenolic Content by LC-ESI-QTOF-MSen_US
dc.typearticleen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.description.wospublicationidWOS:000615937400001en_US
dc.description.scopuspublicationid2-s2.0-85100612332en_US
dc.departmentGümüşhane Üniversitesien_US
dc.authoridAltay, Ahmet / 0000-0001-8120-8900
dc.identifier.volume18en_US
dc.identifier.issue3en_US
dc.identifier.doi10.1002/cbdv.202000812
dc.authorscopusid57221930179
dc.authorscopusid57163218500
dc.authorscopusid39262128900
dc.authorscopusid48861473900
dc.authorscopusid22133807600
dc.authorscopusid35509141500
dc.authorscopusid23972789200
dc.description.pubmedpublicationidPubMed: 33464702en_US


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