Abietane Diterpenes from Hyptis crassifolia Mart. ex Benth. (Lamiaceae)

Detalhes bibliográficos
Autor(a) principal: Lima,Karísia S. B.
Data de Publicação: 2015
Outros Autores: Guedes,Maria L. S., Silveira,Edilberto R.
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=S0103-50532015000100032
Resumo: The phytochemical study of the ethanol extract from roots of Hyptis crassifolia Mart. ex Benth. (Lamiaceae) led to the isolation and structure elucidation of nine diterpenes identified as 11,12,15-trihydroxy-8,11,13-abietatrien-7-one, 6α,11,12,15-tetrahydroxy-8,11,13-abietatrien-7-one, 11,12,16-trihydroxy-17(15→16)-abeo-abieta-8,11,13-trien-7-one, (16S)-12,16-epoxy-11,14-dihydroxy-17(15→16)-abeo-abieta-8,11,13-trien-7-one, incanone, ferruginol, sugiol, 11-oxomanoyl oxide and 11β-hydroxymanoyl oxide. Compounds 11,12,16-trihydroxy-17(15→16)-abeo-abieta-8,11,13-trien-7-one and 6α,11,12,15-tetrahydroxy-8,11,13-abietatrien-7-one are new, 11,12,15-trihydroxy-8,11,13-abietatrien-7-one is being reported for the first time as a new natural abietane diterpene, while for (16S)-12,16-epoxy-11,14-dihydroxy-17(15→16)-abeo-abieta- 8,11,13‑trien-7-one, previously isolated from Teucrium divaricatum Subsp. villosum, a revision of the 1H and 13C nuclear magnetic resonance (NMR) data previously reported is proposed. Structure determination of all constituents was performed by mean of spectroscopic techniques such as high resolution mass spectrometry (HRMS), infrared (IR), 1H and 13C 1D and 2D NMR and comparison with literature data.
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spelling Abietane Diterpenes from Hyptis crassifolia Mart. ex Benth. (Lamiaceae)Hyptis crassifoliaLamiaceaeabietane diterpenesrearranged abietane diterpeneslabdane diterpenesThe phytochemical study of the ethanol extract from roots of Hyptis crassifolia Mart. ex Benth. (Lamiaceae) led to the isolation and structure elucidation of nine diterpenes identified as 11,12,15-trihydroxy-8,11,13-abietatrien-7-one, 6α,11,12,15-tetrahydroxy-8,11,13-abietatrien-7-one, 11,12,16-trihydroxy-17(15→16)-abeo-abieta-8,11,13-trien-7-one, (16S)-12,16-epoxy-11,14-dihydroxy-17(15→16)-abeo-abieta-8,11,13-trien-7-one, incanone, ferruginol, sugiol, 11-oxomanoyl oxide and 11β-hydroxymanoyl oxide. Compounds 11,12,16-trihydroxy-17(15→16)-abeo-abieta-8,11,13-trien-7-one and 6α,11,12,15-tetrahydroxy-8,11,13-abietatrien-7-one are new, 11,12,15-trihydroxy-8,11,13-abietatrien-7-one is being reported for the first time as a new natural abietane diterpene, while for (16S)-12,16-epoxy-11,14-dihydroxy-17(15→16)-abeo-abieta- 8,11,13‑trien-7-one, previously isolated from Teucrium divaricatum Subsp. villosum, a revision of the 1H and 13C nuclear magnetic resonance (NMR) data previously reported is proposed. Structure determination of all constituents was performed by mean of spectroscopic techniques such as high resolution mass spectrometry (HRMS), infrared (IR), 1H and 13C 1D and 2D NMR and comparison with literature data.Sociedade Brasileira de Química2015-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015000100032Journal of the Brazilian Chemical Society v.26 n.1 2015reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20140210info:eu-repo/semantics/openAccessLima,Karísia S. B.Guedes,Maria L. S.Silveira,Edilberto R.eng2015-02-03T00:00:00Zoai:scielo:S0103-50532015000100032Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2015-02-03T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Abietane Diterpenes from Hyptis crassifolia Mart. ex Benth. (Lamiaceae)
title Abietane Diterpenes from Hyptis crassifolia Mart. ex Benth. (Lamiaceae)
spellingShingle Abietane Diterpenes from Hyptis crassifolia Mart. ex Benth. (Lamiaceae)
Lima,Karísia S. B.
Hyptis crassifolia
Lamiaceae
abietane diterpenes
rearranged abietane diterpenes
labdane diterpenes
title_short Abietane Diterpenes from Hyptis crassifolia Mart. ex Benth. (Lamiaceae)
title_full Abietane Diterpenes from Hyptis crassifolia Mart. ex Benth. (Lamiaceae)
title_fullStr Abietane Diterpenes from Hyptis crassifolia Mart. ex Benth. (Lamiaceae)
title_full_unstemmed Abietane Diterpenes from Hyptis crassifolia Mart. ex Benth. (Lamiaceae)
title_sort Abietane Diterpenes from Hyptis crassifolia Mart. ex Benth. (Lamiaceae)
author Lima,Karísia S. B.
author_facet Lima,Karísia S. B.
Guedes,Maria L. S.
Silveira,Edilberto R.
author_role author
author2 Guedes,Maria L. S.
Silveira,Edilberto R.
author2_role author
author
dc.contributor.author.fl_str_mv Lima,Karísia S. B.
Guedes,Maria L. S.
Silveira,Edilberto R.
dc.subject.por.fl_str_mv Hyptis crassifolia
Lamiaceae
abietane diterpenes
rearranged abietane diterpenes
labdane diterpenes
topic Hyptis crassifolia
Lamiaceae
abietane diterpenes
rearranged abietane diterpenes
labdane diterpenes
description The phytochemical study of the ethanol extract from roots of Hyptis crassifolia Mart. ex Benth. (Lamiaceae) led to the isolation and structure elucidation of nine diterpenes identified as 11,12,15-trihydroxy-8,11,13-abietatrien-7-one, 6α,11,12,15-tetrahydroxy-8,11,13-abietatrien-7-one, 11,12,16-trihydroxy-17(15→16)-abeo-abieta-8,11,13-trien-7-one, (16S)-12,16-epoxy-11,14-dihydroxy-17(15→16)-abeo-abieta-8,11,13-trien-7-one, incanone, ferruginol, sugiol, 11-oxomanoyl oxide and 11β-hydroxymanoyl oxide. Compounds 11,12,16-trihydroxy-17(15→16)-abeo-abieta-8,11,13-trien-7-one and 6α,11,12,15-tetrahydroxy-8,11,13-abietatrien-7-one are new, 11,12,15-trihydroxy-8,11,13-abietatrien-7-one is being reported for the first time as a new natural abietane diterpene, while for (16S)-12,16-epoxy-11,14-dihydroxy-17(15→16)-abeo-abieta- 8,11,13‑trien-7-one, previously isolated from Teucrium divaricatum Subsp. villosum, a revision of the 1H and 13C nuclear magnetic resonance (NMR) data previously reported is proposed. Structure determination of all constituents was performed by mean of spectroscopic techniques such as high resolution mass spectrometry (HRMS), infrared (IR), 1H and 13C 1D and 2D NMR and comparison with literature data.
publishDate 2015
dc.date.none.fl_str_mv 2015-01-01
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=S0103-50532015000100032
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015000100032
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0103-5053.20140210
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.26 n.1 2015
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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