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dc.contributor.authorTallini, Luciana Ruschelpt_BR
dc.contributor.authorTorras-Claveria, Laurapt_BR
dc.contributor.authorBorges, Warley de Souzapt_BR
dc.contributor.authorKaiser, Marcelpt_BR
dc.contributor.authorViladomat, Francescpt_BR
dc.contributor.authorZuanazzi, Jose Angelo Silveirapt_BR
dc.contributor.authorBastida, Jaumept_BR
dc.date.accessioned2018-12-18T04:04:02Zpt_BR
dc.date.issued2018pt_BR
dc.identifier.issn1420-3049pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/186260pt_BR
dc.description.abstractNatural products play an important role in the development of new drugs. In this context, the Amaryllidaceae alkaloids have attracted considerable attention in view of their unique structural features and various biological activities. In this study, twenty-three alkaloids were identified from Crinum amabile by GC-MS and two new structures (augustine N-oxide and buphanisine N-oxide) were structurally elucidated by NMR. Anti-parasitic and cholinesterase (AChE and BuChE) inhibitory activities of six alkaloids isolated from this species, including the two new compounds, are described herein. None of the alkaloids isolated from C. amabile gave better results than the reference drugs, so it was possible to conclude that the N-oxide group does not increase their therapeutic potential.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofMolecules. Basel. Vol. 23, no. 6 (2018), artigo 1277pt_BR
dc.rightsOpen Accessen
dc.subjectCrinum amabileen
dc.subjectFarmáciapt_BR
dc.subjectAugustine N-oxideen
dc.subjectBuphanisine N-oxideen
dc.subjectBiological activitiesen
dc.titleN-oxide alkaloids from Crinum amabile (Amaryllidaceae)pt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb001083487pt_BR
dc.type.originEstrangeiropt_BR


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