New biflavonoid and other flavonoids from the leaves of Chimarrhis turbinata and their antioxidant activities

Detalhes bibliográficos
Autor(a) principal: Cardoso,Carmem L.
Data de Publicação: 2005
Outros Autores: Silva,Dulce H. S., Castro-Gamboa,Ian, Bolzani,Vanderlan da S.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000800008
Resumo: A new biflavonol, named chimarrhoside (1), and eight known flavonol glycosides (2-9), were isolated from the leaves of Chimarrhis turbinata. Their structures were established on the basis of 1D and 2D NMR experiments as quercetin-3-O-rutinoside (2), kaempferol-3-O-rutinoside (3), kaempferol-3-O-alpha-L-rhamnopyranosyl-(1->6)- beta-D-galactopyranoside (4), quercetin-3-O-alpha-L-rhamnopyranosyl-(1->6)- beta-D-galactopyranoside (5), 6-hydroxy-rutin (6), kaempferol-3-O-D-galactopyranoside (7), kaempferol-3-O-D-glucopyranoside (8) and kaempferol-3-O-alpha-L-rhamnopyranosyl-(1->6)- alpha-L-rhamnopyranosyl-(1->4)-beta-D-glucopyranoside (9). In addition, catechin (10) and catechin-(4<FONT FACE=Symbol>a®</FONT>8)-catechin-procyanidin B-3) (11) were isolated. The crude extract, fractions and isolated compounds were evaluated for their antioxidative properties using an autographic assay based on beta-carotene bleaching on TLC plates, and spectrophotometric detection by reduction of the stable 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical. Flavonoids 2, 5, 6, 10 and 11 displayed strong free radical scavenging activity, when compared with the standards BHT and rutin.
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spelling New biflavonoid and other flavonoids from the leaves of Chimarrhis turbinata and their antioxidant activitiesRubiaceaechimarrhosideDPPHbeta-caroteneA new biflavonol, named chimarrhoside (1), and eight known flavonol glycosides (2-9), were isolated from the leaves of Chimarrhis turbinata. Their structures were established on the basis of 1D and 2D NMR experiments as quercetin-3-O-rutinoside (2), kaempferol-3-O-rutinoside (3), kaempferol-3-O-alpha-L-rhamnopyranosyl-(1->6)- beta-D-galactopyranoside (4), quercetin-3-O-alpha-L-rhamnopyranosyl-(1->6)- beta-D-galactopyranoside (5), 6-hydroxy-rutin (6), kaempferol-3-O-D-galactopyranoside (7), kaempferol-3-O-D-glucopyranoside (8) and kaempferol-3-O-alpha-L-rhamnopyranosyl-(1->6)- alpha-L-rhamnopyranosyl-(1->4)-beta-D-glucopyranoside (9). In addition, catechin (10) and catechin-(4<FONT FACE=Symbol>a®</FONT>8)-catechin-procyanidin B-3) (11) were isolated. The crude extract, fractions and isolated compounds were evaluated for their antioxidative properties using an autographic assay based on beta-carotene bleaching on TLC plates, and spectrophotometric detection by reduction of the stable 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical. Flavonoids 2, 5, 6, 10 and 11 displayed strong free radical scavenging activity, when compared with the standards BHT and rutin.Sociedade Brasileira de Química2005-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000800008Journal of the Brazilian Chemical Society v.16 n.6b 2005reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532005000800008info:eu-repo/semantics/openAccessCardoso,Carmem L.Silva,Dulce H. S.Castro-Gamboa,IanBolzani,Vanderlan da S.eng2006-01-20T00:00:00Zoai:scielo:S0103-50532005000800008Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2006-01-20T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv New biflavonoid and other flavonoids from the leaves of Chimarrhis turbinata and their antioxidant activities
title New biflavonoid and other flavonoids from the leaves of Chimarrhis turbinata and their antioxidant activities
spellingShingle New biflavonoid and other flavonoids from the leaves of Chimarrhis turbinata and their antioxidant activities
Cardoso,Carmem L.
Rubiaceae
chimarrhoside
DPPH
beta-carotene
title_short New biflavonoid and other flavonoids from the leaves of Chimarrhis turbinata and their antioxidant activities
title_full New biflavonoid and other flavonoids from the leaves of Chimarrhis turbinata and their antioxidant activities
title_fullStr New biflavonoid and other flavonoids from the leaves of Chimarrhis turbinata and their antioxidant activities
title_full_unstemmed New biflavonoid and other flavonoids from the leaves of Chimarrhis turbinata and their antioxidant activities
title_sort New biflavonoid and other flavonoids from the leaves of Chimarrhis turbinata and their antioxidant activities
author Cardoso,Carmem L.
author_facet Cardoso,Carmem L.
Silva,Dulce H. S.
Castro-Gamboa,Ian
Bolzani,Vanderlan da S.
author_role author
author2 Silva,Dulce H. S.
Castro-Gamboa,Ian
Bolzani,Vanderlan da S.
author2_role author
author
author
dc.contributor.author.fl_str_mv Cardoso,Carmem L.
Silva,Dulce H. S.
Castro-Gamboa,Ian
Bolzani,Vanderlan da S.
dc.subject.por.fl_str_mv Rubiaceae
chimarrhoside
DPPH
beta-carotene
topic Rubiaceae
chimarrhoside
DPPH
beta-carotene
description A new biflavonol, named chimarrhoside (1), and eight known flavonol glycosides (2-9), were isolated from the leaves of Chimarrhis turbinata. Their structures were established on the basis of 1D and 2D NMR experiments as quercetin-3-O-rutinoside (2), kaempferol-3-O-rutinoside (3), kaempferol-3-O-alpha-L-rhamnopyranosyl-(1->6)- beta-D-galactopyranoside (4), quercetin-3-O-alpha-L-rhamnopyranosyl-(1->6)- beta-D-galactopyranoside (5), 6-hydroxy-rutin (6), kaempferol-3-O-D-galactopyranoside (7), kaempferol-3-O-D-glucopyranoside (8) and kaempferol-3-O-alpha-L-rhamnopyranosyl-(1->6)- alpha-L-rhamnopyranosyl-(1->4)-beta-D-glucopyranoside (9). In addition, catechin (10) and catechin-(4<FONT FACE=Symbol>a®</FONT>8)-catechin-procyanidin B-3) (11) were isolated. The crude extract, fractions and isolated compounds were evaluated for their antioxidative properties using an autographic assay based on beta-carotene bleaching on TLC plates, and spectrophotometric detection by reduction of the stable 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical. Flavonoids 2, 5, 6, 10 and 11 displayed strong free radical scavenging activity, when compared with the standards BHT and rutin.
publishDate 2005
dc.date.none.fl_str_mv 2005-11-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000800008
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000800008
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532005000800008
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.16 n.6b 2005
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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