Acanthoic acid and other constituents from the stem of Annona amazonica (Annonaceae)
Autor(a) principal: | |
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Data de Publicação: | 2009 |
Outros Autores: | , , , , , , , , , , |
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=S0103-50532009000600015 |
Resumo: | The present work reports the isolation of acanthoic acid, a promising pimaradiene-type diterpene with several important biological activities described in the literature, from the stems of Annona amazonica. We found that acanthoic acid has significant trypanocidal activity against the epimastigote forms of Trypanosoma cruzi. This diterpene is the major constituent of the plant, comprising at least 65% of the hexane extract, demonstrating that A. amazonica is a new renewable natural source for this compound. The chemical investigation also resulted in the isolation of the alkaloids liriodenine and cassythicine, and other compounds including terpenes, sterols, and fatty acids. Additionally, the complete and unequivocal ¹H and 13C NMR chemical shift assignments for cassythicine are provided. |
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Acanthoic acid and other constituents from the stem of Annona amazonica (Annonaceae)Annona amazonicaAnnonaceaeacanthoic acidcassythicinetrypanocidal activityThe present work reports the isolation of acanthoic acid, a promising pimaradiene-type diterpene with several important biological activities described in the literature, from the stems of Annona amazonica. We found that acanthoic acid has significant trypanocidal activity against the epimastigote forms of Trypanosoma cruzi. This diterpene is the major constituent of the plant, comprising at least 65% of the hexane extract, demonstrating that A. amazonica is a new renewable natural source for this compound. The chemical investigation also resulted in the isolation of the alkaloids liriodenine and cassythicine, and other compounds including terpenes, sterols, and fatty acids. Additionally, the complete and unequivocal ¹H and 13C NMR chemical shift assignments for cassythicine are provided.Sociedade Brasileira de Química2009-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000600015Journal of the Brazilian Chemical Society v.20 n.6 2009reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532009000600015info:eu-repo/semantics/openAccessPinheiro,Maria Lúcia B.Xavier,Clahildek M.Souza,Afonso D. L. deRabelo,Diego de MouraBatista,Cristiane L.Batista,Regiane L.Costa,Emmanoel V.Campos,Francinete R.Barison,AnderssonValdez,Rodrigo H.Ueda-Nakamura,TâniaNakamura,Celso V.eng2009-08-04T00:00:00Zoai:scielo:S0103-50532009000600015Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2009-08-04T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Acanthoic acid and other constituents from the stem of Annona amazonica (Annonaceae) |
title |
Acanthoic acid and other constituents from the stem of Annona amazonica (Annonaceae) |
spellingShingle |
Acanthoic acid and other constituents from the stem of Annona amazonica (Annonaceae) Pinheiro,Maria Lúcia B. Annona amazonica Annonaceae acanthoic acid cassythicine trypanocidal activity |
title_short |
Acanthoic acid and other constituents from the stem of Annona amazonica (Annonaceae) |
title_full |
Acanthoic acid and other constituents from the stem of Annona amazonica (Annonaceae) |
title_fullStr |
Acanthoic acid and other constituents from the stem of Annona amazonica (Annonaceae) |
title_full_unstemmed |
Acanthoic acid and other constituents from the stem of Annona amazonica (Annonaceae) |
title_sort |
Acanthoic acid and other constituents from the stem of Annona amazonica (Annonaceae) |
author |
Pinheiro,Maria Lúcia B. |
author_facet |
Pinheiro,Maria Lúcia B. Xavier,Clahildek M. Souza,Afonso D. L. de Rabelo,Diego de Moura Batista,Cristiane L. Batista,Regiane L. Costa,Emmanoel V. Campos,Francinete R. Barison,Andersson Valdez,Rodrigo H. Ueda-Nakamura,Tânia Nakamura,Celso V. |
author_role |
author |
author2 |
Xavier,Clahildek M. Souza,Afonso D. L. de Rabelo,Diego de Moura Batista,Cristiane L. Batista,Regiane L. Costa,Emmanoel V. Campos,Francinete R. Barison,Andersson Valdez,Rodrigo H. Ueda-Nakamura,Tânia Nakamura,Celso V. |
author2_role |
author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Pinheiro,Maria Lúcia B. Xavier,Clahildek M. Souza,Afonso D. L. de Rabelo,Diego de Moura Batista,Cristiane L. Batista,Regiane L. Costa,Emmanoel V. Campos,Francinete R. Barison,Andersson Valdez,Rodrigo H. Ueda-Nakamura,Tânia Nakamura,Celso V. |
dc.subject.por.fl_str_mv |
Annona amazonica Annonaceae acanthoic acid cassythicine trypanocidal activity |
topic |
Annona amazonica Annonaceae acanthoic acid cassythicine trypanocidal activity |
description |
The present work reports the isolation of acanthoic acid, a promising pimaradiene-type diterpene with several important biological activities described in the literature, from the stems of Annona amazonica. We found that acanthoic acid has significant trypanocidal activity against the epimastigote forms of Trypanosoma cruzi. This diterpene is the major constituent of the plant, comprising at least 65% of the hexane extract, demonstrating that A. amazonica is a new renewable natural source for this compound. The chemical investigation also resulted in the isolation of the alkaloids liriodenine and cassythicine, and other compounds including terpenes, sterols, and fatty acids. Additionally, the complete and unequivocal ¹H and 13C NMR chemical shift assignments for cassythicine are provided. |
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=S0103-50532009000600015 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532009000600015 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S0103-50532009000600015 |
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.6 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_ |
1750318169901236224 |