Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMES

Detalhes bibliográficos
Autor(a) principal: Pérez,Elsa M. Rodríguez
Data de Publicação: 2016
Outros Autores: Marante,Francisco J. Toledo, Hernández,Josefa Caballero, Barrera,Jaime Bermejo, Rosas,Francisco J. Estevez
Tipo de documento: Artigo
Idioma: spa
Título da fonte: Química Nova (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422016000400456
Resumo: Lichen substances have more than one phenolic hydroxyl group attached to one or more benzene rings, thus qualifying them as polyphenols. The secondary metabolites isolated from the lichen H. tavaresii have been studied in a bid to find compounds protective against oxidative stress and free radical-induced damage. The compounds were identified based on their MS and 1H-NMR spectra as well as retention factors of TLC analysis. In addition to the previously described metabolites (atranorin, chloroatranorin, physodic and physodalic acids) of H. tavaresii, a further three were identified in its thalli: 2´-O-methylphysodone, isophysodic and ursolic acids. The newly identified compounds of H. tavaresii thalli may be useful in the chemotaxonomic classification of this species. Antioxidant effectiveness of the acetone extract's fractions was measured. The compounds of the active fractions were purified and exhibited 180-800 fold less radical scavenging activity than the reference substance α-(+)-tocopherol in a DPPH• model expressed by IC50 values.
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spelling Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMESHypogymniatavaresiilichendepsidesdepsidonesscavengersLichen substances have more than one phenolic hydroxyl group attached to one or more benzene rings, thus qualifying them as polyphenols. The secondary metabolites isolated from the lichen H. tavaresii have been studied in a bid to find compounds protective against oxidative stress and free radical-induced damage. The compounds were identified based on their MS and 1H-NMR spectra as well as retention factors of TLC analysis. In addition to the previously described metabolites (atranorin, chloroatranorin, physodic and physodalic acids) of H. tavaresii, a further three were identified in its thalli: 2´-O-methylphysodone, isophysodic and ursolic acids. The newly identified compounds of H. tavaresii thalli may be useful in the chemotaxonomic classification of this species. Antioxidant effectiveness of the acetone extract's fractions was measured. The compounds of the active fractions were purified and exhibited 180-800 fold less radical scavenging activity than the reference substance α-(+)-tocopherol in a DPPH• model expressed by IC50 values.Sociedade Brasileira de Química2016-05-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422016000400456Química Nova v.39 n.4 2016reponame:Química Nova (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0100-4042.20160053info:eu-repo/semantics/openAccessPérez,Elsa M. RodríguezMarante,Francisco J. ToledoHernández,Josefa CaballeroBarrera,Jaime BermejoRosas,Francisco J. Estevezspa2016-05-25T00:00:00Zoai:scielo:S0100-40422016000400456Revistahttps://www.scielo.br/j/qn/ONGhttps://old.scielo.br/oai/scielo-oai.phpquimicanova@sbq.org.br1678-70640100-4042opendoar:2016-05-25T00:00Química Nova (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMES
title Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMES
spellingShingle Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMES
Pérez,Elsa M. Rodríguez
Hypogymnia
tavaresii
lichen
depsides
depsidones
scavengers
title_short Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMES
title_full Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMES
title_fullStr Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMES
title_full_unstemmed Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMES
title_sort Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMES
author Pérez,Elsa M. Rodríguez
author_facet Pérez,Elsa M. Rodríguez
Marante,Francisco J. Toledo
Hernández,Josefa Caballero
Barrera,Jaime Bermejo
Rosas,Francisco J. Estevez
author_role author
author2 Marante,Francisco J. Toledo
Hernández,Josefa Caballero
Barrera,Jaime Bermejo
Rosas,Francisco J. Estevez
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Pérez,Elsa M. Rodríguez
Marante,Francisco J. Toledo
Hernández,Josefa Caballero
Barrera,Jaime Bermejo
Rosas,Francisco J. Estevez
dc.subject.por.fl_str_mv Hypogymnia
tavaresii
lichen
depsides
depsidones
scavengers
topic Hypogymnia
tavaresii
lichen
depsides
depsidones
scavengers
description Lichen substances have more than one phenolic hydroxyl group attached to one or more benzene rings, thus qualifying them as polyphenols. The secondary metabolites isolated from the lichen H. tavaresii have been studied in a bid to find compounds protective against oxidative stress and free radical-induced damage. The compounds were identified based on their MS and 1H-NMR spectra as well as retention factors of TLC analysis. In addition to the previously described metabolites (atranorin, chloroatranorin, physodic and physodalic acids) of H. tavaresii, a further three were identified in its thalli: 2´-O-methylphysodone, isophysodic and ursolic acids. The newly identified compounds of H. tavaresii thalli may be useful in the chemotaxonomic classification of this species. Antioxidant effectiveness of the acetone extract's fractions was measured. The compounds of the active fractions were purified and exhibited 180-800 fold less radical scavenging activity than the reference substance α-(+)-tocopherol in a DPPH• model expressed by IC50 values.
publishDate 2016
dc.date.none.fl_str_mv 2016-05-01
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=S0100-40422016000400456
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422016000400456
dc.language.iso.fl_str_mv spa
language spa
dc.relation.none.fl_str_mv 10.5935/0100-4042.20160053
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.4 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
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