New Epimeric Spirostanol and Furostanol-Type Steroidal Saponins from Cestrum laevigatum L.

Detalhes bibliográficos
Autor(a) principal: Ribeiro,Paulo R. V.
Data de Publicação: 2016
Outros Autores: Braz-Filho,Raimundo, Araújo,Ana J., Costa-Lotufo,Letícia V., Souza,Luciana G. S., Nobre Junior,Hélio V., Silva,Cecília R. da, Andrade Neto,João B. de, Silveira,Edilberto R., Lima,Mary Anne S.
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=S0103-50532016001202170
Resumo: Four new epimeric spirostanol and furostanol-type steroidal saponins, (25R,S)-5α-spirostan-2α,3β-diol 3-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranosyl-(1→4)-β-D-galactopyranoside, (25R,S)-5α-spirostan-2α,3β-diol 3-O-β-D-glucopyranosyl-(1→2)-α-L-rhamnopyranosyl-(1→4)-β-D-galactopyranoside, 26-O-β-D-glucopyranosyl-(25R,S)-5α-furost-20-ene,2α,3β-diol 3-O-β-D-galactopyranoside and 26-O-β-D-glucopyranosyl-(25R,S)-5α-furost-20-ene,2α,3β-diol 3-O-β-D-galactopyranosyl-(1→4)-β-D-galactopyranoside, in addition to the known (25R,S)-5α-spirostan-2α,3β-diol 3-O-β-D-galactopyranoside, were isolated from Cestrum laevigatum. Compounds were submitted to cytotoxic activity assays using colorectal adenocarcinoma (HCT-116), human promyelocytic leukemia (HL-60), ovarian carcinoma (OVCAR-8), glioma (SF-295) human cancer cell lines, and the antimicrobial activity was evaluated against Candida parapsilosis, C. albicans, C. krusei, Pseudomonas aeruginosa, Staphylococcus aureus and Bacillus subtilis.
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spelling New Epimeric Spirostanol and Furostanol-Type Steroidal Saponins from Cestrum laevigatum L.Cestrum laevigatumsaponinsspirostanolfurostanolcytotoxicantimicrobialFour new epimeric spirostanol and furostanol-type steroidal saponins, (25R,S)-5α-spirostan-2α,3β-diol 3-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranosyl-(1→4)-β-D-galactopyranoside, (25R,S)-5α-spirostan-2α,3β-diol 3-O-β-D-glucopyranosyl-(1→2)-α-L-rhamnopyranosyl-(1→4)-β-D-galactopyranoside, 26-O-β-D-glucopyranosyl-(25R,S)-5α-furost-20-ene,2α,3β-diol 3-O-β-D-galactopyranoside and 26-O-β-D-glucopyranosyl-(25R,S)-5α-furost-20-ene,2α,3β-diol 3-O-β-D-galactopyranosyl-(1→4)-β-D-galactopyranoside, in addition to the known (25R,S)-5α-spirostan-2α,3β-diol 3-O-β-D-galactopyranoside, were isolated from Cestrum laevigatum. Compounds were submitted to cytotoxic activity assays using colorectal adenocarcinoma (HCT-116), human promyelocytic leukemia (HL-60), ovarian carcinoma (OVCAR-8), glioma (SF-295) human cancer cell lines, and the antimicrobial activity was evaluated against Candida parapsilosis, C. albicans, C. krusei, Pseudomonas aeruginosa, Staphylococcus aureus and Bacillus subtilis.Sociedade Brasileira de Química2016-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532016001202170Journal of the Brazilian Chemical Society v.27 n.12 2016reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20160109info:eu-repo/semantics/openAccessRibeiro,Paulo R. V.Braz-Filho,RaimundoAraújo,Ana J.Costa-Lotufo,Letícia V.Souza,Luciana G. S.Nobre Junior,Hélio V.Silva,Cecília R. daAndrade Neto,João B. deSilveira,Edilberto R.Lima,Mary Anne S.eng2016-12-01T00:00:00Zoai:scielo:S0103-50532016001202170Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2016-12-01T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv New Epimeric Spirostanol and Furostanol-Type Steroidal Saponins from Cestrum laevigatum L.
title New Epimeric Spirostanol and Furostanol-Type Steroidal Saponins from Cestrum laevigatum L.
spellingShingle New Epimeric Spirostanol and Furostanol-Type Steroidal Saponins from Cestrum laevigatum L.
Ribeiro,Paulo R. V.
Cestrum laevigatum
saponins
spirostanol
furostanol
cytotoxic
antimicrobial
title_short New Epimeric Spirostanol and Furostanol-Type Steroidal Saponins from Cestrum laevigatum L.
title_full New Epimeric Spirostanol and Furostanol-Type Steroidal Saponins from Cestrum laevigatum L.
title_fullStr New Epimeric Spirostanol and Furostanol-Type Steroidal Saponins from Cestrum laevigatum L.
title_full_unstemmed New Epimeric Spirostanol and Furostanol-Type Steroidal Saponins from Cestrum laevigatum L.
title_sort New Epimeric Spirostanol and Furostanol-Type Steroidal Saponins from Cestrum laevigatum L.
author Ribeiro,Paulo R. V.
author_facet Ribeiro,Paulo R. V.
Braz-Filho,Raimundo
Araújo,Ana J.
Costa-Lotufo,Letícia V.
Souza,Luciana G. S.
Nobre Junior,Hélio V.
Silva,Cecília R. da
Andrade Neto,João B. de
Silveira,Edilberto R.
Lima,Mary Anne S.
author_role author
author2 Braz-Filho,Raimundo
Araújo,Ana J.
Costa-Lotufo,Letícia V.
Souza,Luciana G. S.
Nobre Junior,Hélio V.
Silva,Cecília R. da
Andrade Neto,João B. de
Silveira,Edilberto R.
Lima,Mary Anne S.
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Ribeiro,Paulo R. V.
Braz-Filho,Raimundo
Araújo,Ana J.
Costa-Lotufo,Letícia V.
Souza,Luciana G. S.
Nobre Junior,Hélio V.
Silva,Cecília R. da
Andrade Neto,João B. de
Silveira,Edilberto R.
Lima,Mary Anne S.
dc.subject.por.fl_str_mv Cestrum laevigatum
saponins
spirostanol
furostanol
cytotoxic
antimicrobial
topic Cestrum laevigatum
saponins
spirostanol
furostanol
cytotoxic
antimicrobial
description Four new epimeric spirostanol and furostanol-type steroidal saponins, (25R,S)-5α-spirostan-2α,3β-diol 3-O-β-D-glucopyranosyl-(1→4)-β-D-galactopyranosyl-(1→4)-β-D-galactopyranoside, (25R,S)-5α-spirostan-2α,3β-diol 3-O-β-D-glucopyranosyl-(1→2)-α-L-rhamnopyranosyl-(1→4)-β-D-galactopyranoside, 26-O-β-D-glucopyranosyl-(25R,S)-5α-furost-20-ene,2α,3β-diol 3-O-β-D-galactopyranoside and 26-O-β-D-glucopyranosyl-(25R,S)-5α-furost-20-ene,2α,3β-diol 3-O-β-D-galactopyranosyl-(1→4)-β-D-galactopyranoside, in addition to the known (25R,S)-5α-spirostan-2α,3β-diol 3-O-β-D-galactopyranoside, were isolated from Cestrum laevigatum. Compounds were submitted to cytotoxic activity assays using colorectal adenocarcinoma (HCT-116), human promyelocytic leukemia (HL-60), ovarian carcinoma (OVCAR-8), glioma (SF-295) human cancer cell lines, and the antimicrobial activity was evaluated against Candida parapsilosis, C. albicans, C. krusei, Pseudomonas aeruginosa, Staphylococcus aureus and Bacillus subtilis.
publishDate 2016
dc.date.none.fl_str_mv 2016-12-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532016001202170
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532016001202170
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0103-5053.20160109
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.27 n.12 2016
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
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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)
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