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Publicação:
NF-κB and Angiogenesis Inhibitors from the Aerial Parts of Chresta martii

dc.contributor.authorQueiroz, Marcos Marçal Ferreira
dc.contributor.authorMonteillier, Aymeric
dc.contributor.authorBerndt, Sarah
dc.contributor.authorMarcourt, Laurence
dc.contributor.authorFranco, Eryvelton De Souza
dc.contributor.authorCarpentier, Gilles
dc.contributor.authorNejad Ebrahimi, Samad
dc.contributor.authorCuendet, Muriel
dc.contributor.authorBolzani, Vanderlan Da Silva [UNESP]
dc.contributor.authorMaia, Maria Bernadete Souza
dc.contributor.authorQueiroz, Emerson Ferreira
dc.contributor.authorWolfender, Jean-Luc
dc.contributor.institutionUniversity of Lausanne
dc.contributor.institutionUniversidade Federal de Pernambuco (UFPE)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.contributor.institutionUniversité Paris Est Créteil
dc.contributor.institutionEvin
dc.date.accessioned2018-12-11T17:38:19Z
dc.date.available2018-12-11T17:38:19Z
dc.date.issued2018-08-24
dc.description.abstractThe ethyl acetate extract of the aerial parts of Chresta martii showed significant in vitro NF-κB inhibition. Bioactivity-guided isolation was undertaken using HPLC microfractionation to localize the active compounds. Different zones of the HPLC chromatogram were linked to NF-κB inhibition. In parallel to this HPLC-based activity profiling, HPLC-PDA-ESI-MS and UHPLC-TOF-HRMS were used for the early identification of some of the compounds present in the extract and to get a complete phytochemical overview. The isolation of the compounds was performed by high-speed counter-current chromatography and further semipreparative HPLC. Using this approach, 14 compounds were isolated, two of them being new sesquiterpene lactones. The structures of the isolated compounds were elucidated by spectroscopic methods including UV, ECD, NMR, and HRMS. All isolated compounds were evaluated for their inhibitory activity of NF-κB and angiogenesis, and compound 2 showed promising NF-κB inhibition activity with an IC50 of 0.7 μM. The isolated compounds 1, 2, 5, 7, and 8 caused a significant reduction in angiogenesis when evaluated by an original 3D in vitro angiogenesis assay.en
dc.description.affiliationSchool of Pharmaceutical Sciences University of Geneva University of Lausanne, Rue Michel-Servet 1
dc.description.affiliationPharmacology of Bioactive Products Federal University of Pernambuco UFPE, Postal code 50670-901
dc.description.affiliationNúcleo de Bioensaios Biossíntese e Ecofisiologia de Produtos Naturais NuBBE Instituto de Química UNESP
dc.description.affiliationLaboratoire CRRET Faculté des Sciences et Technologie Université Paris Est Créteil
dc.description.affiliationDepartment of Phytochemistry Medicinal Plants and Drugs Research Institute Shahid Beheshti University G. C. Evin
dc.description.affiliationUnespNúcleo de Bioensaios Biossíntese e Ecofisiologia de Produtos Naturais NuBBE Instituto de Química UNESP
dc.format.extent1769-1776
dc.identifierhttp://dx.doi.org/10.1021/acs.jnatprod.8b00161
dc.identifier.citationJournal of Natural Products, v. 81, n. 8, p. 1769-1776, 2018.
dc.identifier.doi10.1021/acs.jnatprod.8b00161
dc.identifier.issn1520-6025
dc.identifier.issn0163-3864
dc.identifier.scopus2-s2.0-85052550154
dc.identifier.urihttp://hdl.handle.net/11449/180137
dc.language.isoeng
dc.relation.ispartofJournal of Natural Products
dc.relation.ispartofsjr1,368
dc.relation.ispartofsjr1,368
dc.rights.accessRightsAcesso restrito
dc.sourceScopus
dc.titleNF-κB and Angiogenesis Inhibitors from the Aerial Parts of Chresta martiien
dc.typeArtigo
dspace.entity.typePublication
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Química, Araraquarapt
unesp.departmentQuímica Orgânica - IQARpt

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