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dc.contributor.authorCosta, Jessica O.
dc.contributor.authorBarboza, Rodolfo S.
dc.contributor.authorValente, Ligia M. M.
dc.contributor.authorWolff, Thiago
dc.contributor.authorGomes, Mário
dc.contributor.authorGallo Hermosa, Blanca ORCID
dc.contributor.authorBerrueta Simal, Luis Angel
dc.contributor.authorGuimaraes Andrade, Iris P.
dc.contributor.authorGavino Leopoldino, Daniel
dc.contributor.authorAssuncao Miranda, Iranaia
dc.date.accessioned2021-02-17T09:50:47Z
dc.date.available2021-02-17T09:50:47Z
dc.date.issued2020-10
dc.identifier.citationJournal Of The Brazilian Chemical Society 31(10) : 2104-2113 (2020)es_ES
dc.identifier.issn0103-5053
dc.identifier.issn1678-4790
dc.identifier.urihttp://hdl.handle.net/10810/50199
dc.description.abstractThe leaf MeOH extract of Psychotria leiocarpa (Rubiaceae) showed in vitro non-cytotoxic and anti-dengue virus serotype 2 (DENV2) activity in human hepatocarcinoma cell lineage (HepG2). A one-step and cost-effective reversed-phase solid-phase extraction method based on high-performance liquid chromatography (HPLC) parameters allowed the isolation, directly from this bioactive extract, of the monoterpene indole alkaloids: N-glucopyranosyl vincosamide (1), vincosamide (2) and strictosidinic acid (3). The chemical structures were characterized based on 1D and 2D nuclear magnetic resonance (NMR), UV and high-resolution mass spectra (HRMS). The methodology has also allowed yielding a polyphenolic-rich fraction that was analyzed by high-performance liquid chromatography coupled to diode array detection and electrospray ionization tandem mass spectrometry (HPLC-DAD-ESI-MS/MS) revealing two fiavonol triglycosides (4, 5) and three caffeoylquinic acid isomers (6-8). Compound 3 is reported for the first time in P leiocarpa and all the phenolic compounds (4-8) are described for the first time in the genus Psychotria. Compounds 1-3 showed to be non-cytotoxic and anti-dengue active towards DENV2, highlighting vincosamide (2).es_ES
dc.description.sponsorshipThis work was supported by Fundacao Carlos Chagas Filho de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ), processes No. E-26/111.373/2014 and E-26/203.225/2017. DGL and JOC thank Coordenacao de Aperfeicoamento de Pessoal de Nivel Superior (CAPES), finance code 001, for their fellowships. TW thanks both CAPES and FAPERJ for his fellowships. The authors thank the NMR Lab of the Instituto de Pesquisas em Produtos Naturais, Universidade Federal do Rio de Janeiro for the NMR spectra and MSc Matheus Oliveira, Dr Marcelo M. Pereira and Dr Denise Freire for their support. Technical and staff support provided by SGIker (UPV/EHU, MICINN, GV/EJ, ESF) is also gratefully acknowledged.es_ES
dc.language.isoenges_ES
dc.publisherSociedade Brasileira de Químicaes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectPsychotria leiocarpaes_ES
dc.subjectRubiaceaees_ES
dc.subjectmonoterpene indole alkaloidses_ES
dc.subjectphenolic compoundses_ES
dc.subjectsolid-phase extractiones_ES
dc.subjectanti-dengue activityes_ES
dc.subjectN,Beta-d-Glucopyranosyl vincosamidees_ES
dc.subjectphenolic-compoundses_ES
dc.subjectUncaria-tomentosaes_ES
dc.subjectconstituentses_ES
dc.titleOne-Step Isolation of Monoterpene Indole Alkaloids from Psychotria Leiocarpa Leaves and Their Antiviral Activity on Dengue Virus Type-2es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderThis is an open-access article distributed under the terms of the Creative Commons Attribution License. (CC BY 4.0)es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttp://static.sites.sbq.org.br/jbcs.sbq.org.br/pdf/2019-0602AR.pdfes_ES
dc.identifier.doi10.21577/0103-5053.20200111
dc.departamentoesQuímica analíticaes_ES
dc.departamentoeuKimika analitikoaes_ES


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This is an open-access article distributed under the terms of the Creative Commons Attribution License. (CC BY 4.0)
Except where otherwise noted, this item's license is described as This is an open-access article distributed under the terms of the Creative Commons Attribution License. (CC BY 4.0)