Prenylated flavonoids from roots of Dahlstedtia glaziovii (Fabaceae)

Detalhes bibliográficos
Autor(a) principal: Canzi,Edione F.
Data de Publicação: 2014
Outros Autores: Marques,Francisco A., Teixeira,Sirlei D., Tozzi,Ana Maria G. A., Silva,Marcos J., Duarte,Renata Maria T., Duarte,Marta Cristina T., Ruiz,Ana Lúcia T. G., Monteiro,Paula A., Carvalho,João E. de, Maia,Beatriz Helena L. N. Sales
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=S0103-50532014000600002
Resumo: A phytochemical study of roots of Dahlstedtia glaziovii (Fabaceae) furnished a new dibenzoylmethane (glaziovione), along with eighteen known compounds. Their structures were determined through 1D and 2D nuclear magnetic resonance (NMR) (heteronuclear single quantum coherence, HSQC, and heteronuclear multiple bond correlation, HMBC) and high-resolution mass spectrometry (HRMS) spectral analyses. The antiproliferative activity was investigated for the crude extracts, the dibenzoylmethanes 2'-methoxy-8-(α-α-dimethylallyl)-furano-[4",5":3',4']-dibenzoylmethane, 3,4-methylenedioxy-2'-methoxy-8-(α-α-dimethylallyl)-furano-[4",5":3',4']-dibenzoylmethane and pongamol, and the flavones lanceolatin B, karanjin, pongapin and 3',4'-methylenedioxy-2",2"-dimethylpyrano-[5",6":8,7]-flavone. The dibenzoylmethanes were more active than the flavones.The extracts were evaluated for their antimicrobial effects, but none was shown to be active.
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spelling Prenylated flavonoids from roots of Dahlstedtia glaziovii (Fabaceae)Lonchocarpusprenylated flavonoidsdibenzoylmethaneDahlstedtia glazioviiantiproliferative activityA phytochemical study of roots of Dahlstedtia glaziovii (Fabaceae) furnished a new dibenzoylmethane (glaziovione), along with eighteen known compounds. Their structures were determined through 1D and 2D nuclear magnetic resonance (NMR) (heteronuclear single quantum coherence, HSQC, and heteronuclear multiple bond correlation, HMBC) and high-resolution mass spectrometry (HRMS) spectral analyses. The antiproliferative activity was investigated for the crude extracts, the dibenzoylmethanes 2'-methoxy-8-(α-α-dimethylallyl)-furano-[4",5":3',4']-dibenzoylmethane, 3,4-methylenedioxy-2'-methoxy-8-(α-α-dimethylallyl)-furano-[4",5":3',4']-dibenzoylmethane and pongamol, and the flavones lanceolatin B, karanjin, pongapin and 3',4'-methylenedioxy-2",2"-dimethylpyrano-[5",6":8,7]-flavone. The dibenzoylmethanes were more active than the flavones.The extracts were evaluated for their antimicrobial effects, but none was shown to be active.Sociedade Brasileira de Química2014-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000600002Journal of the Brazilian Chemical Society v.25 n.6 2014reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20140071info:eu-repo/semantics/openAccessCanzi,Edione F.Marques,Francisco A.Teixeira,Sirlei D.Tozzi,Ana Maria G. A.Silva,Marcos J.Duarte,Renata Maria T.Duarte,Marta Cristina T.Ruiz,Ana Lúcia T. G.Monteiro,Paula A.Carvalho,João E. deMaia,Beatriz Helena L. N. Saleseng2014-07-01T00:00:00Zoai:scielo:S0103-50532014000600002Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2014-07-01T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Prenylated flavonoids from roots of Dahlstedtia glaziovii (Fabaceae)
title Prenylated flavonoids from roots of Dahlstedtia glaziovii (Fabaceae)
spellingShingle Prenylated flavonoids from roots of Dahlstedtia glaziovii (Fabaceae)
Canzi,Edione F.
Lonchocarpus
prenylated flavonoids
dibenzoylmethane
Dahlstedtia glaziovii
antiproliferative activity
title_short Prenylated flavonoids from roots of Dahlstedtia glaziovii (Fabaceae)
title_full Prenylated flavonoids from roots of Dahlstedtia glaziovii (Fabaceae)
title_fullStr Prenylated flavonoids from roots of Dahlstedtia glaziovii (Fabaceae)
title_full_unstemmed Prenylated flavonoids from roots of Dahlstedtia glaziovii (Fabaceae)
title_sort Prenylated flavonoids from roots of Dahlstedtia glaziovii (Fabaceae)
author Canzi,Edione F.
author_facet Canzi,Edione F.
Marques,Francisco A.
Teixeira,Sirlei D.
Tozzi,Ana Maria G. A.
Silva,Marcos J.
Duarte,Renata Maria T.
Duarte,Marta Cristina T.
Ruiz,Ana Lúcia T. G.
Monteiro,Paula A.
Carvalho,João E. de
Maia,Beatriz Helena L. N. Sales
author_role author
author2 Marques,Francisco A.
Teixeira,Sirlei D.
Tozzi,Ana Maria G. A.
Silva,Marcos J.
Duarte,Renata Maria T.
Duarte,Marta Cristina T.
Ruiz,Ana Lúcia T. G.
Monteiro,Paula A.
Carvalho,João E. de
Maia,Beatriz Helena L. N. Sales
author2_role author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Canzi,Edione F.
Marques,Francisco A.
Teixeira,Sirlei D.
Tozzi,Ana Maria G. A.
Silva,Marcos J.
Duarte,Renata Maria T.
Duarte,Marta Cristina T.
Ruiz,Ana Lúcia T. G.
Monteiro,Paula A.
Carvalho,João E. de
Maia,Beatriz Helena L. N. Sales
dc.subject.por.fl_str_mv Lonchocarpus
prenylated flavonoids
dibenzoylmethane
Dahlstedtia glaziovii
antiproliferative activity
topic Lonchocarpus
prenylated flavonoids
dibenzoylmethane
Dahlstedtia glaziovii
antiproliferative activity
description A phytochemical study of roots of Dahlstedtia glaziovii (Fabaceae) furnished a new dibenzoylmethane (glaziovione), along with eighteen known compounds. Their structures were determined through 1D and 2D nuclear magnetic resonance (NMR) (heteronuclear single quantum coherence, HSQC, and heteronuclear multiple bond correlation, HMBC) and high-resolution mass spectrometry (HRMS) spectral analyses. The antiproliferative activity was investigated for the crude extracts, the dibenzoylmethanes 2'-methoxy-8-(α-α-dimethylallyl)-furano-[4",5":3',4']-dibenzoylmethane, 3,4-methylenedioxy-2'-methoxy-8-(α-α-dimethylallyl)-furano-[4",5":3',4']-dibenzoylmethane and pongamol, and the flavones lanceolatin B, karanjin, pongapin and 3',4'-methylenedioxy-2",2"-dimethylpyrano-[5",6":8,7]-flavone. The dibenzoylmethanes were more active than the flavones.The extracts were evaluated for their antimicrobial effects, but none was shown to be active.
publishDate 2014
dc.date.none.fl_str_mv 2014-06-01
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=S0103-50532014000600002
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000600002
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0103-5053.20140071
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.25 n.6 2014
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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