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dc.contributor.authorAndrioli, Willian J.-
dc.contributor.authorConti, Raphael-
dc.contributor.authorAraújo, Magali J.-
dc.contributor.authorZanasi, Riccardo-
dc.contributor.authorCavalcanti, Bruno C.-
dc.contributor.authorManfrim, Viviane-
dc.contributor.authorToledo, Juliano S.-
dc.contributor.authorTedesco, Daniele-
dc.contributor.authorMoraes Filho, Manoel Odorico de-
dc.contributor.authorPessoa, Cláudia-
dc.contributor.authorCruz, Angela K.-
dc.contributor.authorBertucci, Carlo-
dc.contributor.authorSabino, José-
dc.contributor.authorNanayakkara, Dhammika N. P.-
dc.contributor.authorBastos, Jairo K.-
dc.date.accessioned2014-02-06T16:17:54Z-
dc.date.available2014-02-06T16:17:54Z-
dc.date.issued2014-01-
dc.identifier.citationANDRIOLI, 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.pt_BR
dc.identifier.issn0163-3864-
dc.identifier.urihttp://www.repositorio.ufc.br/handle/riufc/7214-
dc.description.abstractThree 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.pt_BR
dc.language.isoenpt_BR
dc.publisherJournal of Natural Productspt_BR
dc.subjectCristalografiapt_BR
dc.subjectCitotoxicidade Imunológicapt_BR
dc.titleMycoleptones A−C and polyketides from the endophytem mycoleptodiscus indicuspt_BR
dc.typeArtigo de Periódicopt_BR
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