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

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-i...

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Main Authors: Elsa M. Rodríguez Pérez, Francisco J. Toledo Marante, Josefa Caballero Hernández, Jaime Bermejo Barrera, Francisco J. Estevez Rosas
Format: Article
Language:English
Published: Sociedade Brasileira de Química 2016-05-01
Series:Química Nova
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422016000400456&lng=en&tlng=en
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spelling doaj-d22e1ad5145f47adbf5f0c5677f693ae2020-11-25T01:31:29ZengSociedade Brasileira de QuímicaQuímica Nova1678-70642016-05-0139445646110.5935/0100-4042.20160053S0100-40422016000400456Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMESElsa M. Rodríguez PérezFrancisco J. Toledo MaranteJosefa Caballero HernándezJaime Bermejo BarreraFrancisco J. Estevez RosasLichen 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.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422016000400456&lng=en&tlng=enHypogymniatavaresiilichendepsidesdepsidonesscavengers
collection DOAJ
language English
format Article
sources DOAJ
author Elsa M. Rodríguez Pérez
Francisco J. Toledo Marante
Josefa Caballero Hernández
Jaime Bermejo Barrera
Francisco J. Estevez Rosas
spellingShingle Elsa M. Rodríguez Pérez
Francisco J. Toledo Marante
Josefa Caballero Hernández
Jaime Bermejo Barrera
Francisco J. Estevez Rosas
Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMES
Química Nova
Hypogymnia
tavaresii
lichen
depsides
depsidones
scavengers
author_facet Elsa M. Rodríguez Pérez
Francisco J. Toledo Marante
Josefa Caballero Hernández
Jaime Bermejo Barrera
Francisco J. Estevez Rosas
author_sort Elsa M. Rodríguez Pérez
title Actividad antioxidante de los polifenoles de HYPOGYMNIA TAVARESII D. HAWKSW. & P. JAMES
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
publisher Sociedade Brasileira de Química
series Química Nova
issn 1678-7064
publishDate 2016-05-01
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.
topic Hypogymnia
tavaresii
lichen
depsides
depsidones
scavengers
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422016000400456&lng=en&tlng=en
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