In vitro Antiplasmodial Activities of Alkaloids Isolated from Roots of Worsleya procera (Lem.) Traub (Amaryllidaceae)

dc.contributor.authorGonring-Salarini, Karla L.
dc.contributor.authorConti, Raphael
dc.contributor.authorAndrade, Jean Paulo de
dc.contributor.authorBorges, Bárbara Juliana P.
dc.contributor.authorAguiar, Anna Caroline C.
dc.contributor.authorSouza, Juliana O.
dc.contributor.authorZanini, Camila L.
dc.contributor.authorOliva, Glaucius
dc.contributor.authorTenorio, Juan Carlos
dc.contributor.authorEllena, Javier
dc.contributor.authorBastida Armengol, Jaume
dc.contributor.authorGuido, Rafael V. C.
dc.contributor.authorBorges, Warley S.
dc.date.accessioned2020-07-02T05:49:10Z
dc.date.available2020-07-02T05:49:10Z
dc.date.issued2019-04-11
dc.date.updated2020-07-02T05:49:10Z
dc.description.abstractA combined phytochemical, crystallographic and biological study of Worsleya procera roots was performed. Fifteen alkaloids were identified by gas chromatography mass spectrometry (GC-MS) and seven of them were isolated. The structures of the alkaloids were elucidated by spectroscopic methods, and a detailed crystallographic study of tazettine was carried out. The isolated alkaloids and the obtained extracts were tested in vitro against Plasmodium falciparum (3D7 and K1 strains) and human hepatocarcinoma cells (HepG2) to assess their antiplasmodial and cytotoxic effects, respectively. One of the isolated alkaloid derivatives, lycorine, exhibited antiplasmodial activity against both sensitive (3D7) and resistant (K1) parasite strains in the low micromolar range (half-maximal sample inhibitory concentration (IC50) values of 2.5 and 3.1 µM, respectively) and displayed a low cytotoxicity profile, with a selectivity index greater than 100. Our findings indicate that lycorine is a hit for antimalarial drug discovery. Keywords: isoquinolinic alkaloids; Amaryllidaceae; Plasmodium falciparum; lycorine; tazettine
dc.format.extent10 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec701812
dc.identifier.issn0103-5053
dc.identifier.urihttps://hdl.handle.net/2445/167237
dc.language.isoeng
dc.publisherSociedade Brasileira de Química
dc.relation.isformatofReproducció del document publicat a: https://doi.org/10.21577/0103-5053.20190061
dc.relation.ispartofJournal of the Brazilian Chemical Society, 2019, vol. 30, num. 8, p. 1624-1633
dc.relation.urihttps://doi.org/10.21577/0103-5053.20190061
dc.rightscc-by (c) Sociedade Brasileira de Química, 2019
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
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.classificationAmaril·lidàcies
dc.subject.classificationIsoquinolina
dc.subject.otherAlkaloids
dc.subject.otherAmaryllidaceae
dc.subject.otherIsoquinoline
dc.titleIn vitro Antiplasmodial Activities of Alkaloids Isolated from Roots of Worsleya procera (Lem.) Traub (Amaryllidaceae)
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion

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