Megastimanes and ergostane type steroid from leaves Cratylia mollis (Leguminosae)

Detalhes bibliográficos
Autor(a) principal: Lima,Luciano S.
Data de Publicação: 2009
Outros Autores: Lima,Marcos V. B., David,Juceni P., Giulietti,Ana M., Queiroz,Luciano P. de, David,Jorge M.
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=S0103-50532009001000022
Resumo: From the methanolic extract of the leaves of Cratylia mollis were obtained by chromatographic techniques (3S,5S,6S,9R)-3,6-dihydroxy-5,6-dihydro- β-ionol (1), and a new bis-norisoprenoid named (4S*, 6S*)-4-but-1E-enyl-4,6-dihydroxy-3,5,5-trimethyl-cyclohex-2-enone (2) as well as 5a,8a-epidioxyergosta-6,22-dien-3-β-ol. The structures of the pure compounds were elucidated based on MS, ¹H and 13C NMR spectroscopic data analyses.
id SBQ-2_4c72eb8d2d1833713680abad7acaf505
oai_identifier_str oai:scielo:S0103-50532009001000022
network_acronym_str SBQ-2
network_name_str Journal of the Brazilian Chemical Society (Online)
repository_id_str
spelling Megastimanes and ergostane type steroid from leaves Cratylia mollis (Leguminosae)megastimanesLeguminosaeCratylia mollisFrom the methanolic extract of the leaves of Cratylia mollis were obtained by chromatographic techniques (3S,5S,6S,9R)-3,6-dihydroxy-5,6-dihydro- β-ionol (1), and a new bis-norisoprenoid named (4S*, 6S*)-4-but-1E-enyl-4,6-dihydroxy-3,5,5-trimethyl-cyclohex-2-enone (2) as well as 5a,8a-epidioxyergosta-6,22-dien-3-β-ol. The structures of the pure compounds were elucidated based on MS, ¹H and 13C NMR spectroscopic data analyses.Sociedade Brasileira de Química2009-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009001000022Journal of the Brazilian Chemical Society v.20 n.10 2009reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532009001000022info:eu-repo/semantics/openAccessLima,Luciano S.Lima,Marcos V. B.David,Juceni P.Giulietti,Ana M.Queiroz,Luciano P. deDavid,Jorge M.eng2011-10-14T00:00:00Zoai:scielo:S0103-50532009001000022Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2011-10-14T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Megastimanes and ergostane type steroid from leaves Cratylia mollis (Leguminosae)
title Megastimanes and ergostane type steroid from leaves Cratylia mollis (Leguminosae)
spellingShingle Megastimanes and ergostane type steroid from leaves Cratylia mollis (Leguminosae)
Lima,Luciano S.
megastimanes
Leguminosae
Cratylia mollis
title_short Megastimanes and ergostane type steroid from leaves Cratylia mollis (Leguminosae)
title_full Megastimanes and ergostane type steroid from leaves Cratylia mollis (Leguminosae)
title_fullStr Megastimanes and ergostane type steroid from leaves Cratylia mollis (Leguminosae)
title_full_unstemmed Megastimanes and ergostane type steroid from leaves Cratylia mollis (Leguminosae)
title_sort Megastimanes and ergostane type steroid from leaves Cratylia mollis (Leguminosae)
author Lima,Luciano S.
author_facet Lima,Luciano S.
Lima,Marcos V. B.
David,Juceni P.
Giulietti,Ana M.
Queiroz,Luciano P. de
David,Jorge M.
author_role author
author2 Lima,Marcos V. B.
David,Juceni P.
Giulietti,Ana M.
Queiroz,Luciano P. de
David,Jorge M.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Lima,Luciano S.
Lima,Marcos V. B.
David,Juceni P.
Giulietti,Ana M.
Queiroz,Luciano P. de
David,Jorge M.
dc.subject.por.fl_str_mv megastimanes
Leguminosae
Cratylia mollis
topic megastimanes
Leguminosae
Cratylia mollis
description From the methanolic extract of the leaves of Cratylia mollis were obtained by chromatographic techniques (3S,5S,6S,9R)-3,6-dihydroxy-5,6-dihydro- β-ionol (1), and a new bis-norisoprenoid named (4S*, 6S*)-4-but-1E-enyl-4,6-dihydroxy-3,5,5-trimethyl-cyclohex-2-enone (2) as well as 5a,8a-epidioxyergosta-6,22-dien-3-β-ol. The structures of the pure compounds were elucidated based on MS, ¹H and 13C NMR spectroscopic data analyses.
publishDate 2009
dc.date.none.fl_str_mv 2009-01-01
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=S0103-50532009001000022
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009001000022
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532009001000022
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.20 n.10 2009
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
_version_ 1750318170316472320

Registros relacionados