Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/175967
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dc.contributor.authorLianza, Mariacaterina-
dc.contributor.authorVerdan, Maria Helena-
dc.contributor.authorAndrade, Jean Paulo de-
dc.contributor.authorPoli, Ferruccio-
dc.contributor.authorAlmeida, Larissa C. de-
dc.contributor.authorCosta-Lotufo, Leticia V.-
dc.contributor.authorCunha Neto, Álvaro-
dc.contributor.authorOliveira, Sarah C. C.-
dc.contributor.authorBastida Armengol, Jaume-
dc.contributor.authorBatista, Andrea N. L.-
dc.contributor.authorBatista Jr, João M.-
dc.contributor.authorBorges, Warley S.-
dc.date.accessioned2021-04-01T11:33:42Z-
dc.date.available2021-04-01T11:33:42Z-
dc.date.issued2020-06-01-
dc.identifier.issn0103-5053-
dc.identifier.urihttp://hdl.handle.net/2445/175967-
dc.description.abstractThe phytochemical study of Hippeastrum goianum led to the identification of 13 compounds by means of gas chromatography-mass spectrometry (GC-MS) and nuclear magnetic resonance (NMR). Compounds 7-demethoxy-9-O-methylhostasine (1) and 7-deoxi-trans-dihydronarciclasine (2) had their absolute configurations determined by vibrational circular dichroism (VCD). This is the first time that compound 1 is described in the Amaryllidaceae family. The cytotoxicity of all isolated compounds was tested against colorectal carcinoma (HCT 116), breast carcinoma (MCF-7), and non-tumor human retinal pigment epithelium (RPE) cell lines. The half-maximum inhibitory concentration (IC50) of compound 2 against each cell line was equivalent to the positive control (doxorubicin), indicating a considerable cytotoxic activity. Keywords: narciclasine; galasine; cytotoxic activity; absolute configuration; vibrational circular dichroism-
dc.format.extent11 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSociedade Brasileira de Química-
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.21577/0103-5053.20200116-
dc.relation.ispartofJournal of the Brazilian Chemical Society, 2020, vol. 31, p. 2135-2145-
dc.relation.urihttps://doi.org/10.21577/0103-5053.20200116-
dc.rightscc-by (c) Sociedade Brasileira de Química, 2020-
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es-
dc.sourceArticles publicats en revistes (Biologia, Sanitat i Medi Ambient)-
dc.subject.classificationAlcaloides-
dc.subject.classificationCitotoxicitat per mediació cel·lular-
dc.subject.classificationDicroisme circular-
dc.subject.classificationTumors-
dc.subject.otherAlkaloids-
dc.subject.otherCell-mediated cytotoxicity-
dc.subject.otherCircular dichroism-
dc.subject.otherTumors-
dc.titleIsolation, absolute configuration and cytotoxic activities of alkaloids from Hippeastrum goianum (Ravenna) Meerow (Amaryllidaceae)-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec710167-
dc.date.updated2021-04-01T11:33:42Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Biologia, Sanitat i Medi Ambient)

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