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

Detalhes bibliográficos
Autor(a) principal: Cardoso, Carmem L. [UNESP]
Data de Publicação: 2005
Outros Autores: Silva, Dulce Helena Siqueira [UNESP], Castro-Gamboa, Ian [UNESP], Bolzani, Vanderlan da Silva [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S0103-50532005000800008
http://hdl.handle.net/11449/68467
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-α-L-rhamnopyranosyl-(1→6)-β-D-galactopyranoside (4), quercetin-3-O-α-L-rhamnopyranosyl-(1→6)-β-D- galactopyranoside (5), 6-hydroxy-rutin (6), kaempferol-3-O-D-galactopyranoside (7), kaempferol-3-O-D-glucopyranoside (8) and kaempferol-3-O-α- Lrhamnopyranosyl-(1→6)-α-L-rhamnopyranosyl-(1→4) -β-D-glucopyranoside (9). In addition, catechin (10) and catechin-(4α→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 β-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. ©2005 Sociedade Brasileira de Química.
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spelling New biflavonoid and other flavonoids from the leaves of Chimarrhis turbinata and their antioxidant activitiesβ-caroteneChimarrhosideDPPHRubiaceaeA 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-α-L-rhamnopyranosyl-(1→6)-β-D-galactopyranoside (4), quercetin-3-O-α-L-rhamnopyranosyl-(1→6)-β-D- galactopyranoside (5), 6-hydroxy-rutin (6), kaempferol-3-O-D-galactopyranoside (7), kaempferol-3-O-D-glucopyranoside (8) and kaempferol-3-O-α- Lrhamnopyranosyl-(1→6)-α-L-rhamnopyranosyl-(1→4) -β-D-glucopyranoside (9). In addition, catechin (10) and catechin-(4α→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 β-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. ©2005 Sociedade Brasileira de Química.Instituto de Química Universidade Estadual Paulista, CP 355, 14800-900 Araraquara-SPInstituto de Química Universidade Estadual Paulista, CP 355, 14800-900 Araraquara-SPUniversidade Estadual Paulista (Unesp)Cardoso, Carmem L. [UNESP]Silva, Dulce Helena Siqueira [UNESP]Castro-Gamboa, Ian [UNESP]Bolzani, Vanderlan da Silva [UNESP]2014-05-27T11:21:39Z2014-05-27T11:21:39Z2005-11-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article1353-1359application/pdfhttp://dx.doi.org/10.1590/S0103-50532005000800008Journal of the Brazilian Chemical Society, v. 16, n. 6 B, p. 1353-1359, 2005.0103-5053http://hdl.handle.net/11449/6846710.1590/S0103-50532005000800008S0103-50532005000800008WOS:0002340787000082-s2.0-308444664282-s2.0-30844466428.pdf470200490423124844840836852516730000-0002-1516-7765Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of the Brazilian Chemical Society1.4440,357info:eu-repo/semantics/openAccess2023-12-20T06:23:03Zoai:repositorio.unesp.br:11449/68467Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-12-20T06:23:03Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)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. [UNESP]
β-carotene
Chimarrhoside
DPPH
Rubiaceae
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. [UNESP]
author_facet Cardoso, Carmem L. [UNESP]
Silva, Dulce Helena Siqueira [UNESP]
Castro-Gamboa, Ian [UNESP]
Bolzani, Vanderlan da Silva [UNESP]
author_role author
author2 Silva, Dulce Helena Siqueira [UNESP]
Castro-Gamboa, Ian [UNESP]
Bolzani, Vanderlan da Silva [UNESP]
author2_role author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Cardoso, Carmem L. [UNESP]
Silva, Dulce Helena Siqueira [UNESP]
Castro-Gamboa, Ian [UNESP]
Bolzani, Vanderlan da Silva [UNESP]
dc.subject.por.fl_str_mv β-carotene
Chimarrhoside
DPPH
Rubiaceae
topic β-carotene
Chimarrhoside
DPPH
Rubiaceae
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-α-L-rhamnopyranosyl-(1→6)-β-D-galactopyranoside (4), quercetin-3-O-α-L-rhamnopyranosyl-(1→6)-β-D- galactopyranoside (5), 6-hydroxy-rutin (6), kaempferol-3-O-D-galactopyranoside (7), kaempferol-3-O-D-glucopyranoside (8) and kaempferol-3-O-α- Lrhamnopyranosyl-(1→6)-α-L-rhamnopyranosyl-(1→4) -β-D-glucopyranoside (9). In addition, catechin (10) and catechin-(4α→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 β-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. ©2005 Sociedade Brasileira de Química.
publishDate 2005
dc.date.none.fl_str_mv 2005-11-01
2014-05-27T11:21:39Z
2014-05-27T11:21:39Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0103-50532005000800008
Journal of the Brazilian Chemical Society, v. 16, n. 6 B, p. 1353-1359, 2005.
0103-5053
http://hdl.handle.net/11449/68467
10.1590/S0103-50532005000800008
S0103-50532005000800008
WOS:000234078700008
2-s2.0-30844466428
2-s2.0-30844466428.pdf
4702004904231248
4484083685251673
0000-0002-1516-7765
url http://dx.doi.org/10.1590/S0103-50532005000800008
http://hdl.handle.net/11449/68467
identifier_str_mv Journal of the Brazilian Chemical Society, v. 16, n. 6 B, p. 1353-1359, 2005.
0103-5053
10.1590/S0103-50532005000800008
S0103-50532005000800008
WOS:000234078700008
2-s2.0-30844466428
2-s2.0-30844466428.pdf
4702004904231248
4484083685251673
0000-0002-1516-7765
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Journal of the Brazilian Chemical Society
1.444
0,357
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 1353-1359
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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