CONSTITUINTES QUÍMICOS E ATIVIDADE ANTIOXIDANTE IN VIVO DE FLAVONOIDES ISOLADOS DE Clusia lanceolata (Clusiaceae)
Autor(a) principal: | |
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Data de Publicação: | 2016 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Química Nova (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422016000901093 |
Resumo: | The phytochemical investigation of Clusia lanceolata leaves yielded fourteen compounds including six flavones, vitexin, isovitexin, isovitexin-2"-O-α-L-rhamnopyranoside, vitexin-2"-O-α-L-rhamnopyranoside, orientin and isoorientin, two phaeophytins [132-hydroxy-(132-S-)-phaeophytin a and 132-hydroxy-(132-R)-phaeophytin a], two triterpenes, α- and β-amyrin, and four steroids, β-sitosterol, stigmasterol, sitosterone and stigmasterone. Their structures were assigned based on spectroscopic analysis, including two-dimensional NMR techniques and comparison with literature data. The antioxidant capacity in vivo of vitexin and mixing isovitexin-2"-O-α-L-rhamnopyranoside and vitexin-2"-O-α-L-rhamnopyranoside was evaluated using the yeast Saccharomyces cerevisiae as the biological system model and hydrogen peroxide as a stressor agent. The results showed that the tested flavonoids were able to protect the yeast cell against the oxidative damage caused by H2O2. |
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CONSTITUINTES QUÍMICOS E ATIVIDADE ANTIOXIDANTE IN VIVO DE FLAVONOIDES ISOLADOS DE Clusia lanceolata (Clusiaceae)ClusiaceaeClusia lanceolataflavonoidsantioxidantsSaccharomyces cerevisiaeThe phytochemical investigation of Clusia lanceolata leaves yielded fourteen compounds including six flavones, vitexin, isovitexin, isovitexin-2"-O-α-L-rhamnopyranoside, vitexin-2"-O-α-L-rhamnopyranoside, orientin and isoorientin, two phaeophytins [132-hydroxy-(132-S-)-phaeophytin a and 132-hydroxy-(132-R)-phaeophytin a], two triterpenes, α- and β-amyrin, and four steroids, β-sitosterol, stigmasterol, sitosterone and stigmasterone. Their structures were assigned based on spectroscopic analysis, including two-dimensional NMR techniques and comparison with literature data. The antioxidant capacity in vivo of vitexin and mixing isovitexin-2"-O-α-L-rhamnopyranoside and vitexin-2"-O-α-L-rhamnopyranoside was evaluated using the yeast Saccharomyces cerevisiae as the biological system model and hydrogen peroxide as a stressor agent. The results showed that the tested flavonoids were able to protect the yeast cell against the oxidative damage caused by H2O2.Sociedade Brasileira de Química2016-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422016000901093Química Nova v.39 n.9 2016reponame:Química Nova (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0100-4042.20160131info:eu-repo/semantics/openAccessFerreira,Rafaela O.Carvalho Junior,Almir R. deRiger,Cristiano J.Castro,Rosane N.Silva,Tania M. S. daCarvalho,Mário G. depor2016-11-23T00:00:00Zoai:scielo:S0100-40422016000901093Revistahttps://www.scielo.br/j/qn/ONGhttps://old.scielo.br/oai/scielo-oai.phpquimicanova@sbq.org.br1678-70640100-4042opendoar:2016-11-23T00:00Química Nova (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
CONSTITUINTES QUÍMICOS E ATIVIDADE ANTIOXIDANTE IN VIVO DE FLAVONOIDES ISOLADOS DE Clusia lanceolata (Clusiaceae) |
title |
CONSTITUINTES QUÍMICOS E ATIVIDADE ANTIOXIDANTE IN VIVO DE FLAVONOIDES ISOLADOS DE Clusia lanceolata (Clusiaceae) |
spellingShingle |
CONSTITUINTES QUÍMICOS E ATIVIDADE ANTIOXIDANTE IN VIVO DE FLAVONOIDES ISOLADOS DE Clusia lanceolata (Clusiaceae) Ferreira,Rafaela O. Clusiaceae Clusia lanceolata flavonoids antioxidants Saccharomyces cerevisiae |
title_short |
CONSTITUINTES QUÍMICOS E ATIVIDADE ANTIOXIDANTE IN VIVO DE FLAVONOIDES ISOLADOS DE Clusia lanceolata (Clusiaceae) |
title_full |
CONSTITUINTES QUÍMICOS E ATIVIDADE ANTIOXIDANTE IN VIVO DE FLAVONOIDES ISOLADOS DE Clusia lanceolata (Clusiaceae) |
title_fullStr |
CONSTITUINTES QUÍMICOS E ATIVIDADE ANTIOXIDANTE IN VIVO DE FLAVONOIDES ISOLADOS DE Clusia lanceolata (Clusiaceae) |
title_full_unstemmed |
CONSTITUINTES QUÍMICOS E ATIVIDADE ANTIOXIDANTE IN VIVO DE FLAVONOIDES ISOLADOS DE Clusia lanceolata (Clusiaceae) |
title_sort |
CONSTITUINTES QUÍMICOS E ATIVIDADE ANTIOXIDANTE IN VIVO DE FLAVONOIDES ISOLADOS DE Clusia lanceolata (Clusiaceae) |
author |
Ferreira,Rafaela O. |
author_facet |
Ferreira,Rafaela O. Carvalho Junior,Almir R. de Riger,Cristiano J. Castro,Rosane N. Silva,Tania M. S. da Carvalho,Mário G. de |
author_role |
author |
author2 |
Carvalho Junior,Almir R. de Riger,Cristiano J. Castro,Rosane N. Silva,Tania M. S. da Carvalho,Mário G. de |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Ferreira,Rafaela O. Carvalho Junior,Almir R. de Riger,Cristiano J. Castro,Rosane N. Silva,Tania M. S. da Carvalho,Mário G. de |
dc.subject.por.fl_str_mv |
Clusiaceae Clusia lanceolata flavonoids antioxidants Saccharomyces cerevisiae |
topic |
Clusiaceae Clusia lanceolata flavonoids antioxidants Saccharomyces cerevisiae |
description |
The phytochemical investigation of Clusia lanceolata leaves yielded fourteen compounds including six flavones, vitexin, isovitexin, isovitexin-2"-O-α-L-rhamnopyranoside, vitexin-2"-O-α-L-rhamnopyranoside, orientin and isoorientin, two phaeophytins [132-hydroxy-(132-S-)-phaeophytin a and 132-hydroxy-(132-R)-phaeophytin a], two triterpenes, α- and β-amyrin, and four steroids, β-sitosterol, stigmasterol, sitosterone and stigmasterone. Their structures were assigned based on spectroscopic analysis, including two-dimensional NMR techniques and comparison with literature data. The antioxidant capacity in vivo of vitexin and mixing isovitexin-2"-O-α-L-rhamnopyranoside and vitexin-2"-O-α-L-rhamnopyranoside was evaluated using the yeast Saccharomyces cerevisiae as the biological system model and hydrogen peroxide as a stressor agent. The results showed that the tested flavonoids were able to protect the yeast cell against the oxidative damage caused by H2O2. |
publishDate |
2016 |
dc.date.none.fl_str_mv |
2016-11-01 |
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=S0100-40422016000901093 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422016000901093 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
10.21577/0100-4042.20160131 |
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.39 n.9 2016 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_ |
1750318117908643840 |