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

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Vanessa Gregório
Data de Publicação: 2012
Outros Autores: Duarte, Lucienir Pains, Silva, Grácia Divina de Fátima, Silva, Fernando César, Góes, Jefferson Vieira de, Takahashi, Jacqueline Aparecida, Pimenta, Lúcia Pinheiro Santos, Vieira Filho, Sidney Augusto
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFOP
dARK ID: ark:/61566/0013000000195
Texto Completo: http://www.repositorio.ufop.br/handle/123456789/3856
http://dx.doi.org/10.1590/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 imbricata.Maytenus 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.2014-11-14T18:21:58Z2014-11-14T18:21:58Z2012info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfRODRIGUES, V. G. et al. Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata. Química Nova, v. 35, p. 1375-1380, 2012. Disponível em: <http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422012000700017>. Acesso em: 20 ago. 2014.1678-7064http://www.repositorio.ufop.br/handle/123456789/3856http://dx.doi.org/10.1590/S0100-40422012000700017ark:/61566/0013000000195A Sociedade Brasileira de Química dá permissão à UFOP para reproduzir no RI/UFOP, uma cópia em formato eletrônico dos artigos completos, sem nenhuma edição e/ou modificação, publicados na revista Química Nova, que tenham como autores seus alunos e/ou professores. Fonte: Email do editor de 17 set. 2013.info:eu-repo/semantics/openAccessRodrigues, Vanessa GregórioDuarte, Lucienir PainsSilva, Grácia Divina de FátimaSilva, Fernando CésarGóes, Jefferson Vieira deTakahashi, Jacqueline AparecidaPimenta, Lúcia Pinheiro SantosVieira Filho, Sidney Augustoengreponame:Repositório Institucional da UFOPinstname:Universidade Federal de Ouro Preto (UFOP)instacron:UFOP2024-11-10T13:56:46Zoai:repositorio.ufop.br:123456789/3856Repositório InstitucionalPUBhttp://www.repositorio.ufop.br/oai/requestrepositorio@ufop.edu.bropendoar:32332024-11-10T13:56:46Repositório Institucional da UFOP - Universidade Federal de Ouro Preto (UFOP)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 Gregório
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 Gregório
author_facet Rodrigues, Vanessa Gregório
Duarte, Lucienir Pains
Silva, Grácia Divina de Fátima
Silva, Fernando César
Góes, Jefferson Vieira de
Takahashi, Jacqueline Aparecida
Pimenta, Lúcia Pinheiro Santos
Vieira Filho, Sidney Augusto
author_role author
author2 Duarte, Lucienir Pains
Silva, Grácia Divina de Fátima
Silva, Fernando César
Góes, Jefferson Vieira de
Takahashi, Jacqueline Aparecida
Pimenta, Lúcia Pinheiro Santos
Vieira Filho, Sidney Augusto
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Rodrigues, Vanessa Gregório
Duarte, Lucienir Pains
Silva, Grácia Divina de Fátima
Silva, Fernando César
Góes, Jefferson Vieira de
Takahashi, Jacqueline Aparecida
Pimenta, Lúcia Pinheiro Santos
Vieira Filho, Sidney Augusto
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
2014-11-14T18:21:58Z
2014-11-14T18:21:58Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv RODRIGUES, V. G. et al. Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata. Química Nova, v. 35, p. 1375-1380, 2012. Disponível em: <http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422012000700017>. Acesso em: 20 ago. 2014.
1678-7064
http://www.repositorio.ufop.br/handle/123456789/3856
http://dx.doi.org/10.1590/S0100-40422012000700017
dc.identifier.dark.fl_str_mv ark:/61566/0013000000195
identifier_str_mv RODRIGUES, V. G. et al. Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata. Química Nova, v. 35, p. 1375-1380, 2012. Disponível em: <http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-40422012000700017>. Acesso em: 20 ago. 2014.
1678-7064
ark:/61566/0013000000195
url http://www.repositorio.ufop.br/handle/123456789/3856
http://dx.doi.org/10.1590/S0100-40422012000700017
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:Repositório Institucional da UFOP
instname:Universidade Federal de Ouro Preto (UFOP)
instacron:UFOP
instname_str Universidade Federal de Ouro Preto (UFOP)
instacron_str UFOP
institution UFOP
reponame_str Repositório Institucional da UFOP
collection Repositório Institucional da UFOP
repository.name.fl_str_mv Repositório Institucional da UFOP - Universidade Federal de Ouro Preto (UFOP)
repository.mail.fl_str_mv repositorio@ufop.edu.br
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