Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata

Detalhes bibliográficos
Autor(a) principal: Rodrigues,Vanessa G.
Data de Publicação: 2012
Outros Autores: Duarte,Lucienir P., Silva,Grácia D. F., Silva,Fernando C., Góes,Jefferson V., Takahashi,Jacqueline A., Pimenta,Lúcia P. S., Vieira Filho,Sidney A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Química Nova (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422012000700017
Resumo: The phytochemical study of hexane/ethyl ether (1:1) extract of the roots of M. imbricata, Celastraceae, resulted in the isolation and characterization of six known triterpenes: 11α-hydroxylup-20(29)-en-3-one, previously isolated from this species besides, 3β,11α-di-hydroxylup-20(29)-ene, 3,7-dioxofriedelane, 3-oxo-29-hydroxyfriedelane, tingenone and 6-oxo-tingenol. The chemical structures of these triterpenes were established by spectrometric data (IR, ¹H and 13C NMR) and through comparison with literature data. The hexane/ethyl ether (1:1), ethyl acetate and methanol extracts, and 11α-hydroxylup-20(29)-en-3-one, tingenone and 6-oxo-tingenol, showed antimicrobial properties on in vitro assays. All extracts and triterpenes, except 3β,11α-di-hydroxylup-20(29)-ene, presented toxicity demonstrated by the larvicidal effect test using Artemia salina.
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spelling Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricataMaytenus imbricataCelastraceaepentacyclic triterpenesThe phytochemical study of hexane/ethyl ether (1:1) extract of the roots of M. imbricata, Celastraceae, resulted in the isolation and characterization of six known triterpenes: 11α-hydroxylup-20(29)-en-3-one, previously isolated from this species besides, 3β,11α-di-hydroxylup-20(29)-ene, 3,7-dioxofriedelane, 3-oxo-29-hydroxyfriedelane, tingenone and 6-oxo-tingenol. The chemical structures of these triterpenes were established by spectrometric data (IR, ¹H and 13C NMR) and through comparison with literature data. The hexane/ethyl ether (1:1), ethyl acetate and methanol extracts, and 11α-hydroxylup-20(29)-en-3-one, tingenone and 6-oxo-tingenol, showed antimicrobial properties on in vitro assays. All extracts and triterpenes, except 3β,11α-di-hydroxylup-20(29)-ene, presented toxicity demonstrated by the larvicidal effect test using Artemia salina.Sociedade Brasileira de Química2012-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422012000700017Química Nova v.35 n.7 2012reponame:Química Nova (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0100-40422012000700017info:eu-repo/semantics/openAccessRodrigues,Vanessa G.Duarte,Lucienir P.Silva,Grácia D. F.Silva,Fernando C.Góes,Jefferson V.Takahashi,Jacqueline A.Pimenta,Lúcia P. S.Vieira Filho,Sidney A.eng2012-08-16T00:00:00Zoai:scielo:S0100-40422012000700017Revistahttps://www.scielo.br/j/qn/ONGhttps://old.scielo.br/oai/scielo-oai.phpquimicanova@sbq.org.br1678-70640100-4042opendoar:2012-08-16T00:00Química Nova (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata
title Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata
spellingShingle Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata
Rodrigues,Vanessa G.
Maytenus imbricata
Celastraceae
pentacyclic triterpenes
title_short Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata
title_full Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata
title_fullStr Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata
title_full_unstemmed Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata
title_sort Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata
author Rodrigues,Vanessa G.
author_facet Rodrigues,Vanessa G.
Duarte,Lucienir P.
Silva,Grácia D. F.
Silva,Fernando C.
Góes,Jefferson V.
Takahashi,Jacqueline A.
Pimenta,Lúcia P. S.
Vieira Filho,Sidney A.
author_role author
author2 Duarte,Lucienir P.
Silva,Grácia D. F.
Silva,Fernando C.
Góes,Jefferson V.
Takahashi,Jacqueline A.
Pimenta,Lúcia P. S.
Vieira Filho,Sidney A.
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Rodrigues,Vanessa G.
Duarte,Lucienir P.
Silva,Grácia D. F.
Silva,Fernando C.
Góes,Jefferson V.
Takahashi,Jacqueline A.
Pimenta,Lúcia P. S.
Vieira Filho,Sidney A.
dc.subject.por.fl_str_mv Maytenus imbricata
Celastraceae
pentacyclic triterpenes
topic Maytenus imbricata
Celastraceae
pentacyclic triterpenes
description The phytochemical study of hexane/ethyl ether (1:1) extract of the roots of M. imbricata, Celastraceae, resulted in the isolation and characterization of six known triterpenes: 11α-hydroxylup-20(29)-en-3-one, previously isolated from this species besides, 3β,11α-di-hydroxylup-20(29)-ene, 3,7-dioxofriedelane, 3-oxo-29-hydroxyfriedelane, tingenone and 6-oxo-tingenol. The chemical structures of these triterpenes were established by spectrometric data (IR, ¹H and 13C NMR) and through comparison with literature data. The hexane/ethyl ether (1:1), ethyl acetate and methanol extracts, and 11α-hydroxylup-20(29)-en-3-one, tingenone and 6-oxo-tingenol, showed antimicrobial properties on in vitro assays. All extracts and triterpenes, except 3β,11α-di-hydroxylup-20(29)-ene, presented toxicity demonstrated by the larvicidal effect test using Artemia salina.
publishDate 2012
dc.date.none.fl_str_mv 2012-01-01
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=S0100-40422012000700017
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422012000700017
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0100-40422012000700017
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.35 n.7 2012
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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