Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. Br

Detalhes bibliográficos
Autor(a) principal: Mata,Rosalina C. S.
Data de Publicação: 2011
Outros Autores: Mendonça,Dina I. M. D. de, Vieira,Liliana, Santos,Aldenir F. dos, Silva,Luciana A. da, Gaspar,Jorge F., Martins,Célia, Rueff,José, Sant'Ana,Antônio E. G.
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=S0103-50532011001000008
Resumo: Euphorbia conspicua latex was fractionated into triterpenic and irritant fractions I and II. The triterpenic fraction afforded 15 known compounds and a new triterpene, 3β-(E)-cinnamoyleuphorbol. 20-O-Acetyl-3-O-angeloylingenol was isolated from irritant fraction II. The compounds euphol, 3β-acetoxyeupha-8,24-diene, 3β-(E)-cinnamoyleuphorbol and 20-O-Acetyl-3-O-angeloylingenol were evaluated for molluscicidal activity. 20-O-Acetyl-3-O-angeloylingenol presented LC100 value of 1 mg mL-1, equivalent to that of the standard molluscicide niclosamide. Compounds euphol, 3β-acetoxyeupha-8,24-diene and 3β-(E)-cinnamoyleuphorbol showed low molluscicidal activity. Mutagenic assays (Ames test with strains TA 98, 100 and 102) were performed with 3β-(E)-cinnamoyleuphorbol in the presence and absence of metabolic activation (S9 mix). In V79 cells, the cytotoxicity of 3β-(E)-cinnamoyleuphorbol was evaluated using the MTT assay and the genotoxicity was assessed using the cytokinesis-block micronucleus assay (CBMN) with or without S9 mix. Mutagenic or genotoxic activity was not detected, and no significant cytotoxicity was observed for 3β-(E)-cinnamoyleuphorbol at lower doses.
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spelling Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. BrEuphorbia conspicuamolluscicidal activitymutagenic activitycytotoxic activitygenotoxicity3β-(E)-cinnamoyleuphorbol20-O-acetyl-3-O-angeloylingenolEuphorbia conspicua latex was fractionated into triterpenic and irritant fractions I and II. The triterpenic fraction afforded 15 known compounds and a new triterpene, 3β-(E)-cinnamoyleuphorbol. 20-O-Acetyl-3-O-angeloylingenol was isolated from irritant fraction II. The compounds euphol, 3β-acetoxyeupha-8,24-diene, 3β-(E)-cinnamoyleuphorbol and 20-O-Acetyl-3-O-angeloylingenol were evaluated for molluscicidal activity. 20-O-Acetyl-3-O-angeloylingenol presented LC100 value of 1 mg mL-1, equivalent to that of the standard molluscicide niclosamide. Compounds euphol, 3β-acetoxyeupha-8,24-diene and 3β-(E)-cinnamoyleuphorbol showed low molluscicidal activity. Mutagenic assays (Ames test with strains TA 98, 100 and 102) were performed with 3β-(E)-cinnamoyleuphorbol in the presence and absence of metabolic activation (S9 mix). In V79 cells, the cytotoxicity of 3β-(E)-cinnamoyleuphorbol was evaluated using the MTT assay and the genotoxicity was assessed using the cytokinesis-block micronucleus assay (CBMN) with or without S9 mix. Mutagenic or genotoxic activity was not detected, and no significant cytotoxicity was observed for 3β-(E)-cinnamoyleuphorbol at lower doses.Sociedade Brasileira de Química2011-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011001000008Journal of the Brazilian Chemical Society v.22 n.10 2011reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532011001000008info:eu-repo/semantics/openAccessMata,Rosalina C. S.Mendonça,Dina I. M. D. deVieira,LilianaSantos,Aldenir F. dosSilva,Luciana A. daGaspar,Jorge F.Martins,CéliaRueff,JoséSant'Ana,Antônio E. G.eng2011-10-25T00:00:00Zoai:scielo:S0103-50532011001000008Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2011-10-25T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. Br
title Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. Br
spellingShingle Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. Br
Mata,Rosalina C. S.
Euphorbia conspicua
molluscicidal activity
mutagenic activity
cytotoxic activity
genotoxicity
3β-(E)-cinnamoyleuphorbol
20-O-acetyl-3-O-angeloylingenol
title_short Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. Br
title_full Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. Br
title_fullStr Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. Br
title_full_unstemmed Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. Br
title_sort Molluscicidal Activity of Compounds Isolated from Euphorbia conspicua N. E. Br
author Mata,Rosalina C. S.
author_facet Mata,Rosalina C. S.
Mendonça,Dina I. M. D. de
Vieira,Liliana
Santos,Aldenir F. dos
Silva,Luciana A. da
Gaspar,Jorge F.
Martins,Célia
Rueff,José
Sant'Ana,Antônio E. G.
author_role author
author2 Mendonça,Dina I. M. D. de
Vieira,Liliana
Santos,Aldenir F. dos
Silva,Luciana A. da
Gaspar,Jorge F.
Martins,Célia
Rueff,José
Sant'Ana,Antônio E. G.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Mata,Rosalina C. S.
Mendonça,Dina I. M. D. de
Vieira,Liliana
Santos,Aldenir F. dos
Silva,Luciana A. da
Gaspar,Jorge F.
Martins,Célia
Rueff,José
Sant'Ana,Antônio E. G.
dc.subject.por.fl_str_mv Euphorbia conspicua
molluscicidal activity
mutagenic activity
cytotoxic activity
genotoxicity
3β-(E)-cinnamoyleuphorbol
20-O-acetyl-3-O-angeloylingenol
topic Euphorbia conspicua
molluscicidal activity
mutagenic activity
cytotoxic activity
genotoxicity
3β-(E)-cinnamoyleuphorbol
20-O-acetyl-3-O-angeloylingenol
description Euphorbia conspicua latex was fractionated into triterpenic and irritant fractions I and II. The triterpenic fraction afforded 15 known compounds and a new triterpene, 3β-(E)-cinnamoyleuphorbol. 20-O-Acetyl-3-O-angeloylingenol was isolated from irritant fraction II. The compounds euphol, 3β-acetoxyeupha-8,24-diene, 3β-(E)-cinnamoyleuphorbol and 20-O-Acetyl-3-O-angeloylingenol were evaluated for molluscicidal activity. 20-O-Acetyl-3-O-angeloylingenol presented LC100 value of 1 mg mL-1, equivalent to that of the standard molluscicide niclosamide. Compounds euphol, 3β-acetoxyeupha-8,24-diene and 3β-(E)-cinnamoyleuphorbol showed low molluscicidal activity. Mutagenic assays (Ames test with strains TA 98, 100 and 102) were performed with 3β-(E)-cinnamoyleuphorbol in the presence and absence of metabolic activation (S9 mix). In V79 cells, the cytotoxicity of 3β-(E)-cinnamoyleuphorbol was evaluated using the MTT assay and the genotoxicity was assessed using the cytokinesis-block micronucleus assay (CBMN) with or without S9 mix. Mutagenic or genotoxic activity was not detected, and no significant cytotoxicity was observed for 3β-(E)-cinnamoyleuphorbol at lower doses.
publishDate 2011
dc.date.none.fl_str_mv 2011-10-01
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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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011001000008
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011001000008
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532011001000008
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.22 n.10 2011
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
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instname_str Sociedade Brasileira de Química (SBQ)
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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)
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