New neo-clerodanes from Tinnea antiscorbutica Welv.

Detalhes bibliográficos
Autor(a) principal: Borges,Cristina M. P.
Data de Publicação: 2013
Outros Autores: Mendonça,Dina I. M. D. de, Pinheiro,Sandra C. S., Vieira,Liliana, Mendonça,António J. G., Gaspar,Jorge F., Martins,Célia, Diakanawma,Carlos, Rueff,José
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532013001200008
Resumo: Three new neo-clerodanes, antiscorbuticane A, antiscorbuticane B and antiscorbuticane C, and known compounds glutinol, friedelin, 5,7-dihydroxyflavanone (pinocembrin), 5-hydroxy-3,6,7,4'-tetramethoxyflavone, 5-hydroxy-3,6,7,3',4'-pentamethoxyflavone (artemetin), 5,4'-dihydroxy-3,6,7,3'-tetramethoxyflavone (penduletin) and 5,3',4'-trihydroxy-3,6,7-trimethoxyflavone (chrysosplenol D), were isolated from the methanol extract of Tinnea antiscorbutica. Antiscorbuticane B exhibited no mutagenic activity at doses of up to 250 µg per plate (Ames test) and did not induce micronucleus formation in the V79 cell line at doses of up to 100 µg mL-1.
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spelling New neo-clerodanes from Tinnea antiscorbutica Welv.Tinnea antiscorbuticaneo-clerodanesmutagenic activitycytotoxic activitygenotoxicityThree new neo-clerodanes, antiscorbuticane A, antiscorbuticane B and antiscorbuticane C, and known compounds glutinol, friedelin, 5,7-dihydroxyflavanone (pinocembrin), 5-hydroxy-3,6,7,4'-tetramethoxyflavone, 5-hydroxy-3,6,7,3',4'-pentamethoxyflavone (artemetin), 5,4'-dihydroxy-3,6,7,3'-tetramethoxyflavone (penduletin) and 5,3',4'-trihydroxy-3,6,7-trimethoxyflavone (chrysosplenol D), were isolated from the methanol extract of Tinnea antiscorbutica. Antiscorbuticane B exhibited no mutagenic activity at doses of up to 250 µg per plate (Ames test) and did not induce micronucleus formation in the V79 cell line at doses of up to 100 µg mL-1.Sociedade Brasileira de Química2013-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532013001200008Journal of the Brazilian Chemical Society v.24 n.12 2013reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20130244info:eu-repo/semantics/openAccessBorges,Cristina M. P.Mendonça,Dina I. M. D. dePinheiro,Sandra C. S.Vieira,LilianaMendonça,António J. G.Gaspar,Jorge F.Martins,CéliaDiakanawma,CarlosRueff,Joséeng2013-12-09T00:00:00Zoai:scielo:S0103-50532013001200008Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2013-12-09T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv New neo-clerodanes from Tinnea antiscorbutica Welv.
title New neo-clerodanes from Tinnea antiscorbutica Welv.
spellingShingle New neo-clerodanes from Tinnea antiscorbutica Welv.
Borges,Cristina M. P.
Tinnea antiscorbutica
neo-clerodanes
mutagenic activity
cytotoxic activity
genotoxicity
title_short New neo-clerodanes from Tinnea antiscorbutica Welv.
title_full New neo-clerodanes from Tinnea antiscorbutica Welv.
title_fullStr New neo-clerodanes from Tinnea antiscorbutica Welv.
title_full_unstemmed New neo-clerodanes from Tinnea antiscorbutica Welv.
title_sort New neo-clerodanes from Tinnea antiscorbutica Welv.
author Borges,Cristina M. P.
author_facet Borges,Cristina M. P.
Mendonça,Dina I. M. D. de
Pinheiro,Sandra C. S.
Vieira,Liliana
Mendonça,António J. G.
Gaspar,Jorge F.
Martins,Célia
Diakanawma,Carlos
Rueff,José
author_role author
author2 Mendonça,Dina I. M. D. de
Pinheiro,Sandra C. S.
Vieira,Liliana
Mendonça,António J. G.
Gaspar,Jorge F.
Martins,Célia
Diakanawma,Carlos
Rueff,José
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Borges,Cristina M. P.
Mendonça,Dina I. M. D. de
Pinheiro,Sandra C. S.
Vieira,Liliana
Mendonça,António J. G.
Gaspar,Jorge F.
Martins,Célia
Diakanawma,Carlos
Rueff,José
dc.subject.por.fl_str_mv Tinnea antiscorbutica
neo-clerodanes
mutagenic activity
cytotoxic activity
genotoxicity
topic Tinnea antiscorbutica
neo-clerodanes
mutagenic activity
cytotoxic activity
genotoxicity
description Three new neo-clerodanes, antiscorbuticane A, antiscorbuticane B and antiscorbuticane C, and known compounds glutinol, friedelin, 5,7-dihydroxyflavanone (pinocembrin), 5-hydroxy-3,6,7,4'-tetramethoxyflavone, 5-hydroxy-3,6,7,3',4'-pentamethoxyflavone (artemetin), 5,4'-dihydroxy-3,6,7,3'-tetramethoxyflavone (penduletin) and 5,3',4'-trihydroxy-3,6,7-trimethoxyflavone (chrysosplenol D), were isolated from the methanol extract of Tinnea antiscorbutica. Antiscorbuticane B exhibited no mutagenic activity at doses of up to 250 µg per plate (Ames test) and did not induce micronucleus formation in the V79 cell line at doses of up to 100 µg mL-1.
publishDate 2013
dc.date.none.fl_str_mv 2013-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532013001200008
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0103-5053.20130244
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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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 Journal of the Brazilian Chemical Society v.24 n.12 2013
reponame:Journal of the Brazilian Chemical Society (Online)
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collection Journal of the Brazilian Chemical Society (Online)
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