Please use this identifier to cite or link to this item: http://hdl.handle.net/10884/1324
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dc.contributor.authorMansoor, T.A.-
dc.contributor.authorRamalhete, Cátia-
dc.contributor.authorMulhovo, Silva-
dc.contributor.authorMolnar, Joseph-
dc.contributor.authorFerreira, Maria José-
dc.date.accessioned2018-08-28T11:38:09Z-
dc.date.available2018-08-28T11:38:09Z-
dc.date.issued2009-06-
dc.identifier.urihttp://hdl.handle.net/10884/1324-
dc.description.abstractThree novel beta-carboline indole alkaloids (1-3) have been isolated from a MeOH extract of the leaves of Tabernaemontana elegans. The structures were established by means of spectroscopic techniques including 2D NMR experiments. Compounds 1 and 2 contain a two-carbon unit, attached to a structurally related beta-carboline skeleton, as part of an additional six-membered ring in 1 and a seven-membered ring in 2. To the best of our knowledge, this is the first report of beta-carboline indole alkaloids from the genus Tabernaemontana. Compounds 1-3 were evaluated for their ability to modulate multidrug resistance in mouse lymphoma cell lines. Compounds 1 and 3 exhibited a weak activity.pt_PT
dc.languageeng-
dc.publisherJournal of Natural Productspt_PT
dc.rightsopenAccess-
dc.titleTabernines A-C, beta-carbolines from the leaves of Tabernaemontana elegans.pt_PT
dc.typearticlept_PT
dc.rparessimpt_PT
dc.fimpacto3.885pt_PT
Appears in Collections:A CS/CN - Artigos

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