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dc.contributor.authorGecibesler, I.H. and Demirtas, I. and Koldas, S. and Behcet, L. and Gul, F. and Altun, M.
dc.date.accessioned2021-04-08T12:07:04Z
dc.date.available2021-04-08T12:07:04Z
dc.date.issued2019
dc.identifier10.23751/pn.v21i1-S.5672
dc.identifier.issn11298723
dc.identifier.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85074920826&doi=10.23751%2fpn.v21i1-S.5672&partnerID=40&md5=80271a4a94f3beb23160afefc107d4a3
dc.identifier.urihttp://acikerisim.bingol.edu.tr/handle/20.500.12898/4204
dc.description.abstractPurpose: To reach active compounds from aerial parts of Teucrium chamaedrys L. subsp. sinuatum (TCS) under the guidance of anticancer assay. Methods: The active compounds of T. chamaedrys were isolated using chromatographic techniques including column and preparative thin layer chromatography. Isolated compounds were characterized using 1D and 2D NMR techniques and high-resolution HPLC-TOF/MS. In the present study, we evaluated in vitro antiproliferative activities of isolated compounds from TCS using xCEL-Ligence Real Time Cell Analysis system (RTCA). Findings: Three phenolic compounds, namely luteolin-7-Oglucoside (cinaroside, compound 1), 5, 6, 3'-trihydroxy-7, 4' dimethoxyflavone (nuchensin, compound 2), and (E)-p-coumaroyl-O-β-D-glucoside (compound 3) were isolated for the first time from Teucrium chamaedrys subsp. sinuatum (TCS). The phenolic compounds have antiproliferative effect against the HeLa (Human uterine cancer), C6 (Rat brain tumor) and PC3 (human prostate carcinoma) cells. Conclusions: The results demonstrated that T. chamaedrys subsp. sinuatum and its active components may be suggested as a promising natural antiproliferative agent against HeLa, C6 and PC3 cells. © Mattioli 1885.
dc.language.isoEnglish
dc.sourceProgress in Nutrition
dc.titleBioactivity-guided isolation of compounds with antiproliferative activity from Teucrium chamaedrys L. subsp. sinuatum (Celak.) Rech. f.


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