Logotipo do repositório
 

Publicação:
Fast preparative separation of flavones from capitula of Eriocaulon ligulatum (Vell.) L.B.Smith (Eriocaulaceae) by High-speed countercurrent chromatography (HSCCC)

dc.contributor.authorSantos, Lourdes Campaner dos [UNESP]
dc.contributor.authorSilva, M. A. [UNESP]
dc.contributor.authorRodrigues, C. M. [UNESP]
dc.contributor.authorRodrigues, J. [UNESP]
dc.contributor.authorRinaldo, D. [UNESP]
dc.contributor.authorSannomiya, M. [UNESP]
dc.contributor.authorVilegas, Wagner [UNESP]
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:21:45Z
dc.date.available2014-05-27T11:21:45Z
dc.date.issued2005-12-01
dc.description.abstractHigh-speed countercurrent chromatography (HSCCC) is a leading method for the fast separation of natural products from plants. It was used for the preparative isolation of two flavone monoglucosides present in the capitula of Eriocaulon ligulatum (Veil.) L.B.Smith (Eriocaulaceae). This species, known locally as botão-dourado, is exported to Europe, Japan and North America as an ornamental species, constituting an important source of income for the local population of Minas Gerais State, Brazil. The solvent system, optimized in tests prior to the HSCCC run, consisted of the two phases of the mixture ethyl acetate: n-propanol: water (140:8:80, v/v/v), which led to the successful separation of 6-methoxyluteolin-7-O-β-D-allopyranoside and 6-methoxyapigenin-7-O-β-D-allopyranoside in only 3 hours. The two flavonoids were identified by NMR (1-D and 2-D) and ESI-MS, comparing their spectra with published data.en
dc.description.affiliationDepartamento de Química Orgânica Instituto de Química Universidade Estadual Paulista, Araraquara, SP
dc.description.affiliationDepartamento de Química Orgânica Instituto de Química UNESP, Rua Francisco Degni s/n, 14801-970, Araraquara, SP
dc.description.affiliationUnespDepartamento de Química Orgânica Instituto de Química Universidade Estadual Paulista, Araraquara, SP
dc.description.affiliationUnespDepartamento de Química Orgânica Instituto de Química UNESP, Rua Francisco Degni s/n, 14801-970, Araraquara, SP
dc.format.extent101-103
dc.identifierhttp://serv-bib.fcfar.unesp.br/seer/index.php/Cien_Farm/article/viewArticle/406
dc.identifier.citationRevista de Ciencias Farmaceuticas Basica e Aplicada, v. 26, n. 2, p. 101-103, 2005.
dc.identifier.file2-s2.0-33745675727.pdf
dc.identifier.issn1808-4532
dc.identifier.lattes3538253640602977
dc.identifier.orcid0000-0003-3032-2556
dc.identifier.scopus2-s2.0-33745675727
dc.identifier.urihttp://hdl.handle.net/11449/68639
dc.language.isoeng
dc.relation.ispartofRevista de Ciências Farmacêuticas Básica e Aplicada
dc.relation.ispartofsjr0,131
dc.rights.accessRightsAcesso aberto
dc.sourceScopus
dc.subjectE. ligulatum
dc.subjectEriocaulaceae
dc.subjectFlavone
dc.subjectHSCCC
dc.subject6 methoxyapigenin 7 o beta dextro allopyranoside
dc.subject6 methoxyluteolin 7 o beta dextro allopyranoside
dc.subjectacetic acid ethyl ester
dc.subjectflavanoid
dc.subjectpropanol
dc.subjectunclassified drug
dc.subjectwater
dc.subjectchemical structure
dc.subjectcounter current chromatography
dc.subjectelectrospray mass spectrometry
dc.subjectnuclear magnetic resonance
dc.titleFast preparative separation of flavones from capitula of Eriocaulon ligulatum (Vell.) L.B.Smith (Eriocaulaceae) by High-speed countercurrent chromatography (HSCCC)en
dc.typeArtigo
dcterms.licensehttp://serv-bib.fcfar.unesp.br/seer/index.php/Cien_Farm/about
dspace.entity.typePublication
unesp.author.lattes3538253640602977
unesp.author.orcid0000-0001-5363-6481[5]
unesp.author.orcid0000-0003-3032-2556[7]
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-s2.0-33745675727.pdf
Tamanho:
66.12 KB
Formato:
Adobe Portable Document Format