Mycoleptones A−C and polyketides from the endophytem mycoleptodiscus indicus

Detalhes bibliográficos
Autor(a) principal: Andrioli, Willian J.
Data de Publicação: 2014
Outros Autores: Conti, Raphael, Araújo, Magali J., Zanasi, Riccardo, Cavalcanti, Bruno C., Manfrim, Viviane, Toledo, Juliano S., Tedesco, Daniele, Moraes Filho, Manoel Odorico de, Pessoa, Cláudia, Cruz, Angela K., Bertucci, Carlo, Sabino, José, Nanayakkara, Dhammika N. P., Bastos, Jairo K.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da Universidade Federal do Ceará (UFC)
Texto Completo: http://www.repositorio.ufc.br/handle/riufc/7214
Resumo: Three new azaphilones with an unusual methylene bridge, named mycoleptones A, B, and C (2, 4, and 5), were isolated from cultures of Mycoleptodiscus indicus, a fungus associated with the South American medicinal plant Borreria verticillata. Additionally, four known polyketides, austdiol (1), eugenitin (3), 6-methoxyeugenin (6), and 9- hydroxyeugenin (7), were also isolated. The structural characterization of compounds was carried out by nuclear magnetic resonance spectroscopy, high-resolution mass spectrometry, electronic circular dichroism spectroscopy, timedependent density functional theory calculations, and X-ray crystallography. Compounds 1−9 were weakly active when tested in antileishmanial and cytotoxicity assays.
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spelling Mycoleptones A−C and polyketides from the endophytem mycoleptodiscus indicusCristalografiaCitotoxicidade ImunológicaThree new azaphilones with an unusual methylene bridge, named mycoleptones A, B, and C (2, 4, and 5), were isolated from cultures of Mycoleptodiscus indicus, a fungus associated with the South American medicinal plant Borreria verticillata. Additionally, four known polyketides, austdiol (1), eugenitin (3), 6-methoxyeugenin (6), and 9- hydroxyeugenin (7), were also isolated. The structural characterization of compounds was carried out by nuclear magnetic resonance spectroscopy, high-resolution mass spectrometry, electronic circular dichroism spectroscopy, timedependent density functional theory calculations, and X-ray crystallography. Compounds 1−9 were weakly active when tested in antileishmanial and cytotoxicity assays.Journal of Natural Products2014-02-06T16:17:54Z2014-02-06T16:17:54Z2014-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfANDRIOLI, W. J. et al. Mycoleptones A−C and plyketides from the endophyte mycoleptodiscus indicus. Journal of Natural Products, Cincinnati, Ohio, v. 77, n. 1, p. 70-78, jan. 2014.0163-3864http://www.repositorio.ufc.br/handle/riufc/7214Andrioli, Willian J.Conti, RaphaelAraújo, Magali J.Zanasi, RiccardoCavalcanti, Bruno C.Manfrim, VivianeToledo, Juliano S.Tedesco, DanieleMoraes Filho, Manoel Odorico dePessoa, CláudiaCruz, Angela K.Bertucci, CarloSabino, JoséNanayakkara, Dhammika N. P.Bastos, Jairo K.engreponame:Repositório Institucional da Universidade Federal do Ceará (UFC)instname:Universidade Federal do Ceará (UFC)instacron:UFCinfo:eu-repo/semantics/openAccess2019-11-10T23:01:18Zoai:repositorio.ufc.br:riufc/7214Repositório InstitucionalPUBhttp://www.repositorio.ufc.br/ri-oai/requestbu@ufc.br || repositorio@ufc.bropendoar:2024-09-11T18:41:16.531358Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)false
dc.title.none.fl_str_mv Mycoleptones A−C and polyketides from the endophytem mycoleptodiscus indicus
title Mycoleptones A−C and polyketides from the endophytem mycoleptodiscus indicus
spellingShingle Mycoleptones A−C and polyketides from the endophytem mycoleptodiscus indicus
Andrioli, Willian J.
Cristalografia
Citotoxicidade Imunológica
title_short Mycoleptones A−C and polyketides from the endophytem mycoleptodiscus indicus
title_full Mycoleptones A−C and polyketides from the endophytem mycoleptodiscus indicus
title_fullStr Mycoleptones A−C and polyketides from the endophytem mycoleptodiscus indicus
title_full_unstemmed Mycoleptones A−C and polyketides from the endophytem mycoleptodiscus indicus
title_sort Mycoleptones A−C and polyketides from the endophytem mycoleptodiscus indicus
author Andrioli, Willian J.
author_facet Andrioli, Willian J.
Conti, Raphael
Araújo, Magali J.
Zanasi, Riccardo
Cavalcanti, Bruno C.
Manfrim, Viviane
Toledo, Juliano S.
Tedesco, Daniele
Moraes Filho, Manoel Odorico de
Pessoa, Cláudia
Cruz, Angela K.
Bertucci, Carlo
Sabino, José
Nanayakkara, Dhammika N. P.
Bastos, Jairo K.
author_role author
author2 Conti, Raphael
Araújo, Magali J.
Zanasi, Riccardo
Cavalcanti, Bruno C.
Manfrim, Viviane
Toledo, Juliano S.
Tedesco, Daniele
Moraes Filho, Manoel Odorico de
Pessoa, Cláudia
Cruz, Angela K.
Bertucci, Carlo
Sabino, José
Nanayakkara, Dhammika N. P.
Bastos, Jairo K.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Andrioli, Willian J.
Conti, Raphael
Araújo, Magali J.
Zanasi, Riccardo
Cavalcanti, Bruno C.
Manfrim, Viviane
Toledo, Juliano S.
Tedesco, Daniele
Moraes Filho, Manoel Odorico de
Pessoa, Cláudia
Cruz, Angela K.
Bertucci, Carlo
Sabino, José
Nanayakkara, Dhammika N. P.
Bastos, Jairo K.
dc.subject.por.fl_str_mv Cristalografia
Citotoxicidade Imunológica
topic Cristalografia
Citotoxicidade Imunológica
description Three new azaphilones with an unusual methylene bridge, named mycoleptones A, B, and C (2, 4, and 5), were isolated from cultures of Mycoleptodiscus indicus, a fungus associated with the South American medicinal plant Borreria verticillata. Additionally, four known polyketides, austdiol (1), eugenitin (3), 6-methoxyeugenin (6), and 9- hydroxyeugenin (7), were also isolated. The structural characterization of compounds was carried out by nuclear magnetic resonance spectroscopy, high-resolution mass spectrometry, electronic circular dichroism spectroscopy, timedependent density functional theory calculations, and X-ray crystallography. Compounds 1−9 were weakly active when tested in antileishmanial and cytotoxicity assays.
publishDate 2014
dc.date.none.fl_str_mv 2014-02-06T16:17:54Z
2014-02-06T16:17:54Z
2014-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv ANDRIOLI, W. J. et al. Mycoleptones A−C and plyketides from the endophyte mycoleptodiscus indicus. Journal of Natural Products, Cincinnati, Ohio, v. 77, n. 1, p. 70-78, jan. 2014.
0163-3864
http://www.repositorio.ufc.br/handle/riufc/7214
identifier_str_mv ANDRIOLI, W. J. et al. Mycoleptones A−C and plyketides from the endophyte mycoleptodiscus indicus. Journal of Natural Products, Cincinnati, Ohio, v. 77, n. 1, p. 70-78, jan. 2014.
0163-3864
url http://www.repositorio.ufc.br/handle/riufc/7214
dc.language.iso.fl_str_mv eng
language eng
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Journal of Natural Products
publisher.none.fl_str_mv Journal of Natural Products
dc.source.none.fl_str_mv reponame:Repositório Institucional da Universidade Federal do Ceará (UFC)
instname:Universidade Federal do Ceará (UFC)
instacron:UFC
instname_str Universidade Federal do Ceará (UFC)
instacron_str UFC
institution UFC
reponame_str Repositório Institucional da Universidade Federal do Ceará (UFC)
collection Repositório Institucional da Universidade Federal do Ceará (UFC)
repository.name.fl_str_mv Repositório Institucional da Universidade Federal do Ceará (UFC) - Universidade Federal do Ceará (UFC)
repository.mail.fl_str_mv bu@ufc.br || repositorio@ufc.br
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