dc.contributor.author
Gonring-Salarini, Karla L.
dc.contributor.author
Conti, Raphael
dc.contributor.author
Andrade, Jean Paulo de
dc.contributor.author
Borges, Bárbara Juliana P.
dc.contributor.author
Aguiar, Anna Caroline C.
dc.contributor.author
Souza, Juliana O.
dc.contributor.author
Zanini, Camila L.
dc.contributor.author
Oliva, Glaucius
dc.contributor.author
Tenorio, Juan Carlos
dc.contributor.author
Ellena, Javier
dc.contributor.author
Bastida Armengol, Jaume
dc.contributor.author
Guido, Rafael V. C.
dc.contributor.author
Borges, Warley S.
dc.date.issued
2020-07-02T05:49:10Z
dc.date.issued
2020-07-02T05:49:10Z
dc.date.issued
2019-04-11
dc.date.issued
2020-07-02T05:49:10Z
dc.identifier
https://hdl.handle.net/2445/167237
dc.description.abstract
A 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
application/pdf
dc.format
application/pdf
dc.publisher
Sociedade Brasileira de Química
dc.relation
Reproducció del document publicat a: https://doi.org/10.21577/0103-5053.20190061
dc.relation
Journal of the Brazilian Chemical Society, 2019, vol. 30, num. 8, p. 1624-1633
dc.relation
https://doi.org/10.21577/0103-5053.20190061
dc.rights
cc-by (c) Sociedade Brasileira de Química, 2019
dc.rights
http://creativecommons.org/licenses/by/3.0/es
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Biologia, Sanitat i Medi Ambient)
dc.subject
Amaril·lidàcies
dc.subject
Amaryllidaceae
dc.title
In vitro Antiplasmodial Activities of Alkaloids Isolated from Roots of Worsleya procera (Lem.) Traub (Amaryllidaceae)
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion