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dc.contributor.authorTurkmen, Z
dc.contributor.authorKingston, DGI
dc.contributor.authorKokdil, G
dc.contributor.authorVoelter, W
dc.contributor.authorAdou, E
dc.contributor.authorTopcu, G
dc.date.accessioned2021-03-04T19:12:38Z
dc.date.available2021-03-04T19:12:38Z
dc.date.issued2004
dc.identifier.citationTopcu G., Kokdil G., Turkmen Z., Voelter W., Adou E., Kingston D., "A new clerodane diterpene and other constituents from Ajuga chamaepitys ssp laevigata", ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES, cilt.59, ss.584-588, 2004
dc.identifier.issn0932-0776
dc.identifier.otherav_8e95cba7-9a31-4a94-be1d-de03dda55c02
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/96350
dc.identifier.urihttps://doi.org/10.1515/znb-2004-0518
dc.description.abstractFrom Ajuga chamepitys ssp. laevigata, a new clerodane diterpene, ajugalaevigatic acid, has been isolated besides five known compounds, a diterpene, (13S)-15-hydroxylabd-8(17)-en-19-oic acid, a steroidal glucoside, 3-O-beta-D-glucopyranosyl-stigmasta-5,25-diene, and triterpenes, alpha- and beta-amyrin and ursolic acid. Their structural elucidation is based on NMR and MS spectroscopic analyses. For the new compound 2D NMR experiments were carried out. Ajugalaevigatic acid was tested against a panel of cytotoxic cell lines, and only found to be active against the A2780 human ovarian cancer cell line.
dc.language.isoeng
dc.subjectBiyokimya
dc.subjectTemel Bilimler
dc.subjectBiyoinorganik Kimya
dc.subjectİnorganik Kimya
dc.subjectKİMYA, ORGANİK
dc.subjectTemel Bilimler (SCI)
dc.subjectKimya
dc.subjectKİMYA, İNORGANİK VE NÜKLEER
dc.titleA new clerodane diterpene and other constituents from Ajuga chamaepitys ssp laevigata
dc.typeMakale
dc.relation.journalZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES
dc.contributor.department, ,
dc.identifier.volume59
dc.identifier.issue5
dc.identifier.startpage584
dc.identifier.endpage588
dc.contributor.firstauthorID171621


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