Miscellaneous Diterpenes from the Aerial Parts of Plectranthus ornatus Codd

Detalhes bibliográficos
Autor(a) principal: Ávila,Fábio N.
Data de Publicação: 2017
Outros Autores: Pinto,Francisco C. L., Sousa,Thiciana S., Torres,Maria Conceição M., Costa-Lotufo,Leticia V., Rocha,Danilo D., Vasconcelos,Mayron A. de, Cardoso-Sá,Nairley, Teixeira,Edson H., Albuquerque,Maria Rose Jane R., Silveira,Edilberto R., Pessoa,Otília D. L.
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=S0103-50532017000601014
Resumo: Five new diterpenes derivatives named as ornatin A, B, C, D and E, in addition to six known related diterpenes were isolated from the aerial parts of cultivated specimens of Plectranthus ornatus. The structures were elucidated using a combination of 1D/2D nuclear magnetic resonance (NMR) spectroscopy, high-resolution electrospray ionization mass spectrometry (HRESIMS) and comparison with published NMR data of analogous compounds. All isolated compounds were assayed against four human cancer cell lines, and Gram-positive and Gram-negative bacteria strains. None of them showed any cytotoxic activity, but ornatin C, D, E and three related diterpenes displayed marginal bactericidal or bacteriostatic effects against the Gram-positive strains.
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spelling Miscellaneous Diterpenes from the Aerial Parts of Plectranthus ornatus CoddPlectranthus ornatusditerpenesent-clerodanesbacteriostaticFive new diterpenes derivatives named as ornatin A, B, C, D and E, in addition to six known related diterpenes were isolated from the aerial parts of cultivated specimens of Plectranthus ornatus. The structures were elucidated using a combination of 1D/2D nuclear magnetic resonance (NMR) spectroscopy, high-resolution electrospray ionization mass spectrometry (HRESIMS) and comparison with published NMR data of analogous compounds. All isolated compounds were assayed against four human cancer cell lines, and Gram-positive and Gram-negative bacteria strains. None of them showed any cytotoxic activity, but ornatin C, D, E and three related diterpenes displayed marginal bactericidal or bacteriostatic effects against the Gram-positive strains.Sociedade Brasileira de Química2017-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017000601014Journal of the Brazilian Chemical Society v.28 n.6 2017reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20160255info:eu-repo/semantics/openAccessÁvila,Fábio N.Pinto,Francisco C. L.Sousa,Thiciana S.Torres,Maria Conceição M.Costa-Lotufo,Leticia V.Rocha,Danilo D.Vasconcelos,Mayron A. deCardoso-Sá,NairleyTeixeira,Edson H.Albuquerque,Maria Rose Jane R.Silveira,Edilberto R.Pessoa,Otília D. L.eng2017-05-11T00:00:00Zoai:scielo:S0103-50532017000601014Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2017-05-11T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Miscellaneous Diterpenes from the Aerial Parts of Plectranthus ornatus Codd
title Miscellaneous Diterpenes from the Aerial Parts of Plectranthus ornatus Codd
spellingShingle Miscellaneous Diterpenes from the Aerial Parts of Plectranthus ornatus Codd
Ávila,Fábio N.
Plectranthus ornatus
diterpenes
ent-clerodanes
bacteriostatic
title_short Miscellaneous Diterpenes from the Aerial Parts of Plectranthus ornatus Codd
title_full Miscellaneous Diterpenes from the Aerial Parts of Plectranthus ornatus Codd
title_fullStr Miscellaneous Diterpenes from the Aerial Parts of Plectranthus ornatus Codd
title_full_unstemmed Miscellaneous Diterpenes from the Aerial Parts of Plectranthus ornatus Codd
title_sort Miscellaneous Diterpenes from the Aerial Parts of Plectranthus ornatus Codd
author Ávila,Fábio N.
author_facet Ávila,Fábio N.
Pinto,Francisco C. L.
Sousa,Thiciana S.
Torres,Maria Conceição M.
Costa-Lotufo,Leticia V.
Rocha,Danilo D.
Vasconcelos,Mayron A. de
Cardoso-Sá,Nairley
Teixeira,Edson H.
Albuquerque,Maria Rose Jane R.
Silveira,Edilberto R.
Pessoa,Otília D. L.
author_role author
author2 Pinto,Francisco C. L.
Sousa,Thiciana S.
Torres,Maria Conceição M.
Costa-Lotufo,Leticia V.
Rocha,Danilo D.
Vasconcelos,Mayron A. de
Cardoso-Sá,Nairley
Teixeira,Edson H.
Albuquerque,Maria Rose Jane R.
Silveira,Edilberto R.
Pessoa,Otília D. L.
author2_role author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Ávila,Fábio N.
Pinto,Francisco C. L.
Sousa,Thiciana S.
Torres,Maria Conceição M.
Costa-Lotufo,Leticia V.
Rocha,Danilo D.
Vasconcelos,Mayron A. de
Cardoso-Sá,Nairley
Teixeira,Edson H.
Albuquerque,Maria Rose Jane R.
Silveira,Edilberto R.
Pessoa,Otília D. L.
dc.subject.por.fl_str_mv Plectranthus ornatus
diterpenes
ent-clerodanes
bacteriostatic
topic Plectranthus ornatus
diterpenes
ent-clerodanes
bacteriostatic
description Five new diterpenes derivatives named as ornatin A, B, C, D and E, in addition to six known related diterpenes were isolated from the aerial parts of cultivated specimens of Plectranthus ornatus. The structures were elucidated using a combination of 1D/2D nuclear magnetic resonance (NMR) spectroscopy, high-resolution electrospray ionization mass spectrometry (HRESIMS) and comparison with published NMR data of analogous compounds. All isolated compounds were assayed against four human cancer cell lines, and Gram-positive and Gram-negative bacteria strains. None of them showed any cytotoxic activity, but ornatin C, D, E and three related diterpenes displayed marginal bactericidal or bacteriostatic effects against the Gram-positive strains.
publishDate 2017
dc.date.none.fl_str_mv 2017-06-01
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=S0103-50532017000601014
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532017000601014
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.21577/0103-5053.20160255
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 Journal of the Brazilian Chemical Society v.28 n.6 2017
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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