Antioxidant activities of isolated compounds from stems of Mimosa invisa Mart. ex Colla

Detalhes bibliográficos
Autor(a) principal: Aguiar,Rosane M.
Data de Publicação: 2012
Outros Autores: Alves,Clayton Q., David,Jorge M., Rezende,Larissa C. de, Lima,Luciano S., David,Juceni P., Queiróz,Luciano P. de
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Química Nova (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422012000300024
Resumo: This work describes the phytochemical study of stems of Mimosa invisa (Mimosaceae) and the evaluation of the antioxidant potential of isolated compounds. Cromatografic techniques were employed to isolate salicifoliol, pinoresinol, quercetin, quercetin-3-O-rhamnopyranosyl, quercetin-3-O-arabinofuranosyl lupeol, β-amyrin, sitosterol, p-hydroxy coumaric acid, 4-hydroxy-3-methoxy benzaldehyde (vanillin), 4-hydroxy-3,5-dimethoxy benzaldehyde, 4-hydroxy-3-methoxy benzoic acid and 4',6,7- trimethoxy flavonol. The latter had been previously described but the spectrometric data shown indicated the structure required review. The antioxidant activity of the compounds was evaluated by the DPPH test and capability of NBT reduction by superoxide radicals. Quercetin glycosides showed lower antioxidant potential than quercetin and, salicifoliol was found to be more active than pinoresinol.
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spelling Antioxidant activities of isolated compounds from stems of Mimosa invisa Mart. ex CollaMimosa invisalignans4',6,7-trimethoxyflavonolThis work describes the phytochemical study of stems of Mimosa invisa (Mimosaceae) and the evaluation of the antioxidant potential of isolated compounds. Cromatografic techniques were employed to isolate salicifoliol, pinoresinol, quercetin, quercetin-3-O-rhamnopyranosyl, quercetin-3-O-arabinofuranosyl lupeol, β-amyrin, sitosterol, p-hydroxy coumaric acid, 4-hydroxy-3-methoxy benzaldehyde (vanillin), 4-hydroxy-3,5-dimethoxy benzaldehyde, 4-hydroxy-3-methoxy benzoic acid and 4',6,7- trimethoxy flavonol. The latter had been previously described but the spectrometric data shown indicated the structure required review. The antioxidant activity of the compounds was evaluated by the DPPH test and capability of NBT reduction by superoxide radicals. Quercetin glycosides showed lower antioxidant potential than quercetin and, salicifoliol was found to be more active than pinoresinol.Sociedade Brasileira de Química2012-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422012000300024Química Nova v.35 n.3 2012reponame:Química Nova (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0100-40422012000300024info:eu-repo/semantics/openAccessAguiar,Rosane M.Alves,Clayton Q.David,Jorge M.Rezende,Larissa C. deLima,Luciano S.David,Juceni P.Queiróz,Luciano P. deeng2012-04-24T00:00:00Zoai:scielo:S0100-40422012000300024Revistahttps://www.scielo.br/j/qn/ONGhttps://old.scielo.br/oai/scielo-oai.phpquimicanova@sbq.org.br1678-70640100-4042opendoar:2012-04-24T00:00Química Nova (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Antioxidant activities of isolated compounds from stems of Mimosa invisa Mart. ex Colla
title Antioxidant activities of isolated compounds from stems of Mimosa invisa Mart. ex Colla
spellingShingle Antioxidant activities of isolated compounds from stems of Mimosa invisa Mart. ex Colla
Aguiar,Rosane M.
Mimosa invisa
lignans
4',6,7-trimethoxyflavonol
title_short Antioxidant activities of isolated compounds from stems of Mimosa invisa Mart. ex Colla
title_full Antioxidant activities of isolated compounds from stems of Mimosa invisa Mart. ex Colla
title_fullStr Antioxidant activities of isolated compounds from stems of Mimosa invisa Mart. ex Colla
title_full_unstemmed Antioxidant activities of isolated compounds from stems of Mimosa invisa Mart. ex Colla
title_sort Antioxidant activities of isolated compounds from stems of Mimosa invisa Mart. ex Colla
author Aguiar,Rosane M.
author_facet Aguiar,Rosane M.
Alves,Clayton Q.
David,Jorge M.
Rezende,Larissa C. de
Lima,Luciano S.
David,Juceni P.
Queiróz,Luciano P. de
author_role author
author2 Alves,Clayton Q.
David,Jorge M.
Rezende,Larissa C. de
Lima,Luciano S.
David,Juceni P.
Queiróz,Luciano P. de
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Aguiar,Rosane M.
Alves,Clayton Q.
David,Jorge M.
Rezende,Larissa C. de
Lima,Luciano S.
David,Juceni P.
Queiróz,Luciano P. de
dc.subject.por.fl_str_mv Mimosa invisa
lignans
4',6,7-trimethoxyflavonol
topic Mimosa invisa
lignans
4',6,7-trimethoxyflavonol
description This work describes the phytochemical study of stems of Mimosa invisa (Mimosaceae) and the evaluation of the antioxidant potential of isolated compounds. Cromatografic techniques were employed to isolate salicifoliol, pinoresinol, quercetin, quercetin-3-O-rhamnopyranosyl, quercetin-3-O-arabinofuranosyl lupeol, β-amyrin, sitosterol, p-hydroxy coumaric acid, 4-hydroxy-3-methoxy benzaldehyde (vanillin), 4-hydroxy-3,5-dimethoxy benzaldehyde, 4-hydroxy-3-methoxy benzoic acid and 4',6,7- trimethoxy flavonol. The latter had been previously described but the spectrometric data shown indicated the structure required review. The antioxidant activity of the compounds was evaluated by the DPPH test and capability of NBT reduction by superoxide radicals. Quercetin glycosides showed lower antioxidant potential than quercetin and, salicifoliol was found to be more active than pinoresinol.
publishDate 2012
dc.date.none.fl_str_mv 2012-01-01
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=S0100-40422012000300024
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422012000300024
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0100-40422012000300024
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 Química Nova v.35 n.3 2012
reponame:Química Nova (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Química Nova (Online)
collection Química Nova (Online)
repository.name.fl_str_mv Química Nova (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv quimicanova@sbq.org.br
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