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Publicação:
Dereplication by HPLC-DAD-ESI-MS/MS and Screening for Biological Activities of Byrsonima Species (Malpighiaceae)

dc.contributor.authorFraige, Karina [UNESP]
dc.contributor.authorDametto, Alessandra Cristina [UNESP]
dc.contributor.authorZeraik, Maria Luiza [UNESP]
dc.contributor.authorde Freitas, Larissa [UNESP]
dc.contributor.authorSaraiva, Amanda Correia [UNESP]
dc.contributor.authorMedeiros, Alexandra Ivo [UNESP]
dc.contributor.authorCastro-Gamboa, Ian [UNESP]
dc.contributor.authorCavalheiro, Alberto José [UNESP]
dc.contributor.authorSilva, Dulce Helena S. [UNESP]
dc.contributor.authorLopes, Norberto Peporine
dc.contributor.authorBolzani, Vanderlan S. [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)
dc.contributor.institutionUniversidade de São Paulo (USP)
dc.date.accessioned2018-12-11T17:17:41Z
dc.date.available2018-12-11T17:17:41Z
dc.date.issued2018-03-01
dc.description.abstractIntroduction: Byrsonima species have been used in the treatment of gastrointestinal and gynecological inflammations, skin infections and snakebites. Based on their biological activities, it is important to study other organisms from this genus and to identify their metabolites. Objectives: To determine the metabolic fingerprinting of methanol and ethyl acetate extracts of four Byrsonima species (B. intermedia, B. coccolobifolia, B. verbascifolia and B. sericea) by HPLC-DAD-ESI-MS/MS and evaluate their in vitro antioxidant, anti-glycation, anti-inflammatory and cytotoxic activities. Materials and methods: Antioxidant activity was determined by DPPH˙, ABTS˙+ and ROO˙ scavenging assays. Anti-glycation activity was evaluated by the ability to inhibit the formation of advanced glycation endproducts (AGEs). Anti-inflammatory activity was evaluated using a murine macrophage cell line (RAW 264–7) in the presence of lipopolysaccharide (LPS). Tumour necrosis factor alpha (TNF-α) and nitrite (NO2 −) production were measured by ELISA and the Griess reaction, respectively. The compounds present in the extracts were tentatively identified by HPLC-DAD-ESI-MS/MS. Results: The evaluation of the biological activities showed the potential of the extracts. The activities were assigned to the presence of glycoside flavonoids mainly derived from quercetin, quinic acid derivatives, gallic acid derivatives, galloylquinic acids and proanthocyanidins. Two isomers of sinapic acid-O-hexoside were described for the first time in a Byrsonima species. Conclusion: This research contributes to the study of the genus, it is the first report of the chemical composition of B. sericea and demonstrates the importance of the dereplication process, allowing the identification of known compounds without time-consuming procedures. Copyright © 2017 John Wiley & Sons, Ltd.en
dc.description.affiliationDepartamento de Química Orgânica Instituto de Química de Araraquara Núcleo de Bioensaios Biossíntese e Ecofisiologia de Produtos Naturais (NUBBE) Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP)
dc.description.affiliationDepartamento de Química Universidade Estadual de Londrina (UEL)
dc.description.affiliationDepartamento de Ciências Biológicas Universidade Estadual Paulista (UNESP) Faculdade de Ciências Farmacêuticas Araraquara
dc.description.affiliationDepartamento de Física e Química Faculdade de Ciências Farmacêuticas de Ribeirão Preto Núcleo de Pesquisa em Produtos Naturais e Sintéticos (NPPNS) Universidade de São Paulo (USP)
dc.description.affiliationUnespDepartamento de Química Orgânica Instituto de Química de Araraquara Núcleo de Bioensaios Biossíntese e Ecofisiologia de Produtos Naturais (NUBBE) Universidade Estadual Paulista Júlio de Mesquita Filho (UNESP)
dc.description.affiliationUnespDepartamento de Ciências Biológicas Universidade Estadual Paulista (UNESP) Faculdade de Ciências Farmacêuticas Araraquara
dc.description.sponsorshipFundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)
dc.description.sponsorshipIdFAPESP: 2013/07600-3
dc.description.sponsorshipIdFAPESP: 2013/15086-8
dc.format.extent196-204
dc.identifierhttp://dx.doi.org/10.1002/pca.2734
dc.identifier.citationPhytochemical Analysis, v. 29, n. 2, p. 196-204, 2018.
dc.identifier.doi10.1002/pca.2734
dc.identifier.issn1099-1565
dc.identifier.issn0958-0344
dc.identifier.lattes4702004904231248
dc.identifier.orcid0000-0002-1516-7765
dc.identifier.scopus2-s2.0-85041387400
dc.identifier.urihttp://hdl.handle.net/11449/175816
dc.language.isoeng
dc.relation.ispartofPhytochemical Analysis
dc.relation.ispartofsjr0,841
dc.relation.ispartofsjr0,841
dc.rights.accessRightsAcesso restritopt
dc.sourceScopus
dc.subjectanti-glycation activity
dc.subjectanti-inflammatory activity
dc.subjectByrsonima
dc.subjectdereplication
dc.subjectHPLC-DAD-ESI-MS/MS
dc.titleDereplication by HPLC-DAD-ESI-MS/MS and Screening for Biological Activities of Byrsonima Species (Malpighiaceae)en
dc.typeArtigopt
dspace.entity.typePublication
relation.isDepartmentOfPublication5004bcab-94af-4939-b980-091ae9d0a19e
relation.isDepartmentOfPublication.latestForDiscovery5004bcab-94af-4939-b980-091ae9d0a19e
unesp.author.lattes4702004904231248[9]
unesp.author.lattes2518006820764120[8]
unesp.author.lattes8756770929017974[6]
unesp.author.orcid0000-0002-8298-6568[1]
unesp.author.orcid0000-0003-0615-8776[11]
unesp.author.orcid0000-0002-1516-7765[9]
unesp.author.orcid0000-0001-8214-9957[8]
unesp.author.orcid0000-0001-6048-3647[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentCiências Biológicas - FCFpt
unesp.departmentQuímica Orgânica - IQARpt

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