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dc.contributor.authorDelazar, A
dc.contributor.authorByres, M
dc.contributor.authorGibbons, S
dc.contributor.authorKumarasamy, Y
dc.contributor.authorModarresi, M
dc.contributor.authorNahar, L
dc.contributor.authorShoeb, M
dc.contributor.authorSarker, SD
dc.date.accessioned2018-08-26T06:34:22Z
dc.date.available2018-08-26T06:34:22Z
dc.date.issued2004
dc.identifier.urihttp://dspace.tbzmed.ac.ir:8080/xmlui/handle/123456789/43975
dc.description.abstractReversed-phase preparative HPLC of a methanol extract of the rhizomes of Eremostachys glabra yielded three new iridoid glycosides, namely, 6,9-epi-8-O-acetylshanziside methyl ester, 5,9-epi-penstemoside, and 5,9-epi-7,8-didehydropenstemoside. Their structures were elucidated on the basis of spectroscopic data interpretation. The free-radical scavenging activity of these compounds was assessed using the DPPH assay.
dc.language.isoEnglish
dc.relation.ispartofJournal of natural products
dc.subjectChromatography, High Pressure Liquid
dc.subjectFree Radical Scavengers
dc.subjectGlycosides
dc.subjectIran
dc.subjectIridoid Glycosides
dc.subjectIridoids
dc.subjectLamiaceae
dc.subjectMolecular Structure
dc.subjectNuclear Magnetic Resonance, Biomolecular
dc.subjectPlants, Medicinal
dc.subjectRhizome
dc.titleIridoid glycosides from Eremostachys glabra.
dc.typearticle
dc.citation.volume67
dc.citation.issue9
dc.citation.spage1584
dc.citation.epage7
dc.citation.indexPubmed
dc.identifier.DOIhttps://doi.org/10.1021/np040044b


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