Antioxidant activities of isolated compounds from stems of Mimosa invisa Mart. ex Colla
Autor(a) principal: | |
---|---|
Data de Publicação: | 2012 |
Outros Autores: | , , , , , |
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. |
id |
SBQ-3_0a2a9fc152c66c4602c1cd61cb2d0c59 |
---|---|
oai_identifier_str |
oai:scielo:S0100-40422012000300024 |
network_acronym_str |
SBQ-3 |
network_name_str |
Química Nova (Online) |
repository_id_str |
|
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 |
_version_ |
1750318113155448832 |