Oxygenated bisabolane fucosides from Carthamus lanatus L.

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dc.identifier.uri http://dx.doi.org/10.15488/2458
dc.identifier.uri http://www.repo.uni-hannover.de/handle/123456789/2484
dc.contributor.author Mikhova, Bozhanka
dc.contributor.author Duddeck, Helmut
dc.contributor.author Taskova, Rilka M.
dc.contributor.author Mitova, Maya
dc.contributor.author Alipieva, Kalina
dc.date.accessioned 2017-11-24T11:46:29Z
dc.date.available 2017-11-24T11:46:29Z
dc.date.issued 2004
dc.identifier.citation Mikhova, B.; Duddeck, H.; Taskova, R.; Mitova, M.; Alipieva, K.: Oxygenated bisabolane fucosides from Carthamus lanatus L.. In: Zeitschrift für Naturforschung - Section C Journal of Biosciences 59 (2004), Nr. 3-4, S. 244-248. DOI: https://doi.org/10.1515/znc-2004-3-422
dc.description.abstract The aerial parts of Carthamus lanatus (Asteraceae) afforded four new oxygenated bisabolane fucosides, 10-hydroperoxy-bisabola-2,11-diene 7-O-β-D-fucopyranoside, 11-hydroperoxy-bisabola-2,9-diene 7-O-β-D-fucopyranoside, 10-hydroxy-bisabola-2,11-diene 7-O-β-D- fucopyranoside and 11-hydroxy-bisabola-2,9-diene 7-O-β-D-fucopyranoside together with the known compounds α-bisabolol β-D-fucopyranoside, asperuloside, sitosterol 3-O-β-D-glucoside and stigmasterol 3-O-β-D-glucoside. Asperuloside appears to be the second representative of the iridoid monoterpene group found in the plant family Asteraceae, which until recently was considered to lack iridoids. The main constituent α-bisabolol fucoside exhibited noticeable antibacterial and cytotoxic activities. eng
dc.language.iso eng
dc.publisher Berlin : De Gruyter
dc.relation.ispartofseries Zeitschrift für Naturforschung - Section C Journal of Biosciences 59 (2004), Nr. 3-4
dc.rights CC BY-NC-ND 3.0 Unported
dc.rights.uri https://creativecommons.org/licenses/by-nc-nd/3.0/
dc.subject Asperuloside eng
dc.subject Carthamus lanatus eng
dc.subject Sesquiterpene Fucosides eng
dc.subject antiinfective agent eng
dc.subject drug derivative eng
dc.subject fucose eng
dc.subject plant extract eng
dc.subject sesquiterpene eng
dc.subject article eng
dc.subject Candida eng
dc.subject Carthamus eng
dc.subject chemical structure eng
dc.subject chemistry eng
dc.subject conformation eng
dc.subject drug effect eng
dc.subject electrospray mass spectrometry eng
dc.subject Escherichia coli eng
dc.subject history eng
dc.subject isolation and purification eng
dc.subject microbiological examination eng
dc.subject nuclear magnetic resonance spectroscopy eng
dc.subject oxidation reduction reaction eng
dc.subject plant eng
dc.subject Staphylococcus aureus eng
dc.subject Anti-Infective Agents eng
dc.subject Candida eng
dc.subject Carthamus eng
dc.subject Escherichia coli eng
dc.subject Fucose eng
dc.subject History, 18th Century eng
dc.subject Magnetic Resonance Spectroscopy eng
dc.subject Microbial Sensitivity Tests eng
dc.subject Models, Molecular eng
dc.subject Molecular Conformation eng
dc.subject Molecular Structure eng
dc.subject Oxidation-Reduction eng
dc.subject Plant Components, Aerial eng
dc.subject Plant Extracts eng
dc.subject Sesquiterpenes eng
dc.subject Spectrometry, Mass, Electrospray Ionization eng
dc.subject Staphylococcus aureus eng
dc.subject Asteraceae eng
dc.subject Candida eng
dc.subject Carthamus eng
dc.subject Carthamus lanatus eng
dc.subject Escherichia coli eng
dc.subject Staphylococcus eng
dc.subject Staphylococcus aureus eng
dc.subject.ddc 570 | Biowissenschaften, Biologie ger
dc.title Oxygenated bisabolane fucosides from Carthamus lanatus L.
dc.type Article
dc.type Text
dc.relation.essn 1865-7125
dc.relation.issn 0939-5075
dc.relation.doi https://doi.org/10.1515/znc-2004-3-422
dc.bibliographicCitation.issue 3-4
dc.bibliographicCitation.volume 59
dc.bibliographicCitation.firstPage 244
dc.bibliographicCitation.lastPage 248
dc.description.version publishedVersion
tib.accessRights frei zug�nglich


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