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dc.contributor.authorCarrero, Diego A. S.-
dc.contributor.authorBatista, Pedro H. J.-
dc.contributor.authorSouza, Luciana G. S.-
dc.contributor.authorPinto, Francisco C. L.-
dc.contributor.authorVasconcelos, Mayron A. de-
dc.contributor.authorTeixeira, Edson H.-
dc.contributor.authorCanuto, Kirley Marques-
dc.contributor.authorSantiago, Gilvandete M. P.-
dc.contributor.authorSilveira, Edilberto R.-
dc.contributor.authorPessoa, Otília D. L.-
dc.date.accessioned2018-01-18T14:38:21Z-
dc.date.available2018-01-18T14:38:21Z-
dc.date.issued2018-
dc.identifier.citationCARRERO, D. A. S. et al. Withanolides from leaves of nicandra physalodes. Journal of the Brazilian Chemical Society, São Paulo, v. 29, n. 1, 11-16, 2018.pt_BR
dc.identifier.issn0103-5053-
dc.identifier.urihttp://www.repositorio.ufc.br/handle/riufc/29077-
dc.description.abstractFive new withanolides, designated as 15-oxo-nicaphysalin B, 6 β ,7 α -dihydroxynicandrenone 10, 24 α ,25 β -dihydroxy-nicandrenone-2 and a mixture of the epimers 17-(1 α /1 β -methylpropanone)- nicandrenone, in addition to six known others, were isolated from the leaf acetone extract from Nicandra physalodes . The complete structures of the five new withanolides, particularly their relative stereochemistries, were established by extensive spectroscopic analyses, including 1D and 2D nuclear magnetic resonance (NMR) and high-resolution electrospray ionization mass spectrometry (HRESIMS). The main isolated withanolides were evaluated for their antibacterial, antifungal and larvicidal properties, but, except nicandrenone, which showed marginal larvicidal activity, none of them was active.pt_BR
dc.language.isoenpt_BR
dc.publisherJournal of the Brazilian Chemical Societypt_BR
dc.subjectSolanaceaept_BR
dc.subjectEspectroscopia de Ressonância Magnéticapt_BR
dc.titleWithanolides from leaves of Nicandra physalodespt_BR
dc.typeArtigo de Periódicopt_BR
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