Evaluation of antimicrobial activity and toxic potential of extracts and triterpenes isolated from Maytenus imbricata.
Autor(a) principal: | |
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Data de Publicação: | 2012 |
Outros Autores: | , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UFOP |
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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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/S0100-40422012000700017A 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:UFOP2019-05-09T17:55:22Zoai:repositorio.ufop.br:123456789/3856Repositório InstitucionalPUBhttp://www.repositorio.ufop.br/oai/requestrepositorio@ufop.edu.bropendoar:32332019-05-09T17:55:22Repositório 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 |
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 |
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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1813002796354502656 |