Antioxidants, quinone reductase inducers and acetylcholinesterase inhibitors from Spondias tuberosa fruits

dc.contributor.authorZeraik, Maria Luiza [UNESP]
dc.contributor.authorQueiroz, Emerson Ferreira
dc.contributor.authorMarcourt, Laurence
dc.contributor.authorCiclet, Olivier
dc.contributor.authorCastro-Gamboa, Ian [UNESP]
dc.contributor.authorSilva, Dulce Helena Siqueira [UNESP]
dc.contributor.authorCuendet, Muriel
dc.contributor.authorda Silva Bolzani, Vanderlan [UNESP]
dc.contributor.authorWolfender, Jean-Luc
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversity of Lausanne
dc.date.accessioned2018-12-11T17:00:46Z
dc.date.available2018-12-11T17:00:46Z
dc.date.issued2016-03-01
dc.description.abstractThe methanolic extract of umbu (Spondias tuberosa) presented high antioxidant activities in the DPPH, ABTS and ORAC assays, as well as acetylcholinesterase (AChE) inhibition activity. The dichloromethane extract exhibited cancer chemopreventive activity, with a quinone reductase induction in Hepa1c1c7 cells. The localization of the active compounds was performed by HPLC activity-based profiling, and preliminary structural information was obtained by HPLC-PAD-ESI-MS and UHPLC-TOF-HRMS. The main constituents from the methanolic extract were efficiently isolated in a single step by preparative MPLC-UV. Two new natural products were identified, together with five known compounds. The structures of the compounds were elucidated by 2D NMR and ESI-HRMS. The dichloromethane extract was fractionated by SPE and by semi-preparative HPLC-UV-ELSD. Using this approach, one anacardic acid derivative was isolated. However, this compound was not responsible for QR induction. This study highlights the potential of umbu as an active ingredient for functional food formulations.en
dc.description.affiliationNucleus of Bioassays Biosynthesis and Ecophysiology of Natural Products (NuBBE) Department of Organic Chemistry Institute of Chemistry São Paulo State University (UNESP), P. O. Box 355
dc.description.affiliationSchool of Pharmaceutical Sciences University of Geneva University of Lausanne
dc.description.affiliationUnespNucleus of Bioassays Biosynthesis and Ecophysiology of Natural Products (NuBBE) Department of Organic Chemistry Institute of Chemistry São Paulo State University (UNESP), P. O. Box 355
dc.format.extent396-405
dc.identifierhttp://dx.doi.org/10.1016/j.jff.2015.12.009
dc.identifier.citationJournal of Functional Foods, v. 21, p. 396-405.
dc.identifier.doi10.1016/j.jff.2015.12.009
dc.identifier.file2-s2.0-84957878267.pdf
dc.identifier.issn1756-4646
dc.identifier.lattes4702004904231248
dc.identifier.orcid0000-0002-1516-7765
dc.identifier.scopus2-s2.0-84957878267
dc.identifier.urihttp://hdl.handle.net/11449/172518
dc.language.isoeng
dc.relation.ispartofJournal of Functional Foods
dc.relation.ispartofsjr1,245
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectAcetylcholinesterase inhibition
dc.subjectAntioxidant activity
dc.subjectCancer chemopreventive activity
dc.subjectQuinone reductase induction
dc.subjectSpondias tuberosa fruits
dc.subjectUHPLC/TOF/MS
dc.titleAntioxidants, quinone reductase inducers and acetylcholinesterase inhibitors from Spondias tuberosa fruitsen
dc.typeArtigo
unesp.author.lattes4702004904231248[5]
unesp.author.orcid0000-0002-1516-7765[5]
unesp.campusUniversidade Estadual Paulista (Unesp), Instituto de Química, Araraquarapt
unesp.departmentQuímica Orgânica - IQARpt

Arquivos

Pacote Original

Agora exibindo 1 - 1 de 1
Carregando...
Imagem de Miniatura
Nome:
2-s2.0-84957878267.pdf
Tamanho:
774.1 KB
Formato:
Adobe Portable Document Format
Descrição: