Constituíntes fenólicos polares de Schinus terebinthifolius Raddi (Anacardiaceae)

Detalhes bibliográficos
Autor(a) principal: Ceruks,Melina
Data de Publicação: 2007
Outros Autores: Romoff,Paulete, Fávero,Oriana A., Lago,João Henrique G.
Tipo de documento: Artigo
Idioma: por
Título da fonte: Química Nova (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422007000300018
Resumo: The EtOH extract from the leaves of Schinus terebinthifolius showed anti-radicalar potential in the DPPH test. It was partitioned between n-BuOH:H2O (1:1) and these two phases were also evaluated for anti-radicalar activity. The active n-BuOH phase was partitioned between EtOAc:H2O (1:1) and the active EtOAc phase was submitted to chromatographic procedures to afford five active phenolic compounds: ethyl gallate, methyl gallate, quercitrin, myricetrin and myricetin. The structures of these compounds were established by NMR spectral data analysis.
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spelling Constituíntes fenólicos polares de Schinus terebinthifolius Raddi (Anacardiaceae)Schinus terebinthifoliusphenolic compoundsanti-radicalar potentialThe EtOH extract from the leaves of Schinus terebinthifolius showed anti-radicalar potential in the DPPH test. It was partitioned between n-BuOH:H2O (1:1) and these two phases were also evaluated for anti-radicalar activity. The active n-BuOH phase was partitioned between EtOAc:H2O (1:1) and the active EtOAc phase was submitted to chromatographic procedures to afford five active phenolic compounds: ethyl gallate, methyl gallate, quercitrin, myricetrin and myricetin. The structures of these compounds were established by NMR spectral data analysis.Sociedade Brasileira de Química2007-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422007000300018Química Nova v.30 n.3 2007reponame:Química Nova (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0100-40422007000300018info:eu-repo/semantics/openAccessCeruks,MelinaRomoff,PauleteFávero,Oriana A.Lago,João Henrique G.por2007-05-28T00:00:00Zoai:scielo:S0100-40422007000300018Revistahttps://www.scielo.br/j/qn/ONGhttps://old.scielo.br/oai/scielo-oai.phpquimicanova@sbq.org.br1678-70640100-4042opendoar:2007-05-28T00:00Química Nova (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Constituíntes fenólicos polares de Schinus terebinthifolius Raddi (Anacardiaceae)
title Constituíntes fenólicos polares de Schinus terebinthifolius Raddi (Anacardiaceae)
spellingShingle Constituíntes fenólicos polares de Schinus terebinthifolius Raddi (Anacardiaceae)
Ceruks,Melina
Schinus terebinthifolius
phenolic compounds
anti-radicalar potential
title_short Constituíntes fenólicos polares de Schinus terebinthifolius Raddi (Anacardiaceae)
title_full Constituíntes fenólicos polares de Schinus terebinthifolius Raddi (Anacardiaceae)
title_fullStr Constituíntes fenólicos polares de Schinus terebinthifolius Raddi (Anacardiaceae)
title_full_unstemmed Constituíntes fenólicos polares de Schinus terebinthifolius Raddi (Anacardiaceae)
title_sort Constituíntes fenólicos polares de Schinus terebinthifolius Raddi (Anacardiaceae)
author Ceruks,Melina
author_facet Ceruks,Melina
Romoff,Paulete
Fávero,Oriana A.
Lago,João Henrique G.
author_role author
author2 Romoff,Paulete
Fávero,Oriana A.
Lago,João Henrique G.
author2_role author
author
author
dc.contributor.author.fl_str_mv Ceruks,Melina
Romoff,Paulete
Fávero,Oriana A.
Lago,João Henrique G.
dc.subject.por.fl_str_mv Schinus terebinthifolius
phenolic compounds
anti-radicalar potential
topic Schinus terebinthifolius
phenolic compounds
anti-radicalar potential
description The EtOH extract from the leaves of Schinus terebinthifolius showed anti-radicalar potential in the DPPH test. It was partitioned between n-BuOH:H2O (1:1) and these two phases were also evaluated for anti-radicalar activity. The active n-BuOH phase was partitioned between EtOAc:H2O (1:1) and the active EtOAc phase was submitted to chromatographic procedures to afford five active phenolic compounds: ethyl gallate, methyl gallate, quercitrin, myricetrin and myricetin. The structures of these compounds were established by NMR spectral data analysis.
publishDate 2007
dc.date.none.fl_str_mv 2007-06-01
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=S0100-40422007000300018
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422007000300018
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv 10.1590/S0100-40422007000300018
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.30 n.3 2007
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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