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dc.contributor.authorOzgen, Ufuk
dc.contributor.authorSevindik, Handan
dc.contributor.authorKazaz, Cavit
dc.contributor.authorYigit, Demet
dc.contributor.authorKandemir, Ali
dc.contributor.authorSecen, Hasan
dc.contributor.authorCalis, Ihsan
dc.date.accessioned2019-12-16T07:56:36Z
dc.date.available2019-12-16T07:56:36Z
dc.date.issued2010
dc.identifier.issn1420-3049
dc.identifier.urihttps://doi.org/10.3390/molecules15042593
dc.identifier.urihttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257313/
dc.identifier.urihttp://hdl.handle.net/11655/19261
dc.description.abstractSonchus erzincanicus (Asteraceae) is an endemic species in Turkey, where six Sonchus species grow. In this study, a phytochemical study was performed on the aerial parts of the plant. The study describes the isolation and structure elucidation of five flavonoids and two α-ionone glycosides from S. erzincanicus. The compounds were isolated using several and repeated chromatographic techniques from ethyl acetate and aqueous phases that were partitioned from a methanol extract obtained from the plant. 5,7,3′,4′-Tetrahydroxy-3-methoxyflavone (1) and quercetin 3-O-β-D-glucoside (2) were isolated from the ethyl acetate phase, while corchoionoside C 6’-O-sulfate (3), corchoionoside C (4), luteolin 7-O-glucuronide (5) and luteolin 7-O-β-D-glucoside (6), apigenin 7-O-glucuronide (7) were isolated from the aqueous phase. Corchoionoside C 6’-O-sulfate (3), isolated for the first time from a natural source, was a new compound. The structures of the compounds were elucidated by means of 1H-NMR, 13C-NMR, 2D-NMR (COSY, HMQC, HMBC) and ESI-MS.
dc.relation.isversionof10.3390/molecules15042593
dc.rightsinfo:eu-repo/semantics/openAccess
dc.titleA New Sulfated Α-Ionone Glycoside from Sonchus Erzincanicus Matthews
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.relation.journalMolecules
dc.contributor.departmentBiyoloji
dc.identifier.volume15
dc.identifier.issue4
dc.identifier.startpage2593
dc.identifier.endpage2599
dc.description.indexPubMed
dc.description.indexWoS
dc.description.indexScopus


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