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dc.contributor.authorLima, Nerilson M.-
dc.contributor.authorCursino-Hron, Lorena M.-
dc.contributor.authorLima, Alita Moura-
dc.contributor.authorSouza, João Vicente Braga de-
dc.contributor.authorOliveira, André C. de-
dc.contributor.authorMarinho, Jane Vasconcelos N.-
dc.contributor.authorNunez, C. V.-
dc.date.accessioned2020-05-15T14:34:13Z-
dc.date.available2020-05-15T14:34:13Z-
dc.date.issued2018-
dc.identifier.urihttps://repositorio.inpa.gov.br/handle/1/15597-
dc.description.abstractCandida spp. is associated with almost 80% of all nosocomial fungal infections and is considered a major cause of blood stream infections. In humans, Cryptococcosis is a disease of the lungs caused by the fungi Cryptococcus gattii and Cryptococcus neoformans. It can be potentially fatal, especially in immune-compromised patients. In a search for antifungal drugs, Deguelia duckeana extracts were assayed against these two fungi and also against Candida albicans, which causes candidiasis. Hexane branches and CH2Cl2 root extracts as well as the substances 4-hydroxylonchocarpine, 3,5,4′-trimethoxy-4-prenylstilbene and 3′,4′-methylenedioxy-7-methoxyflavone were assayed to determine the minimal inhibitory concentration. Phytochemical study of CH2Cl2 root and hexane branch extracts from D. duckeana A.M.G. Azevedo, Fabaceae, resulted in the isolation and characterization of nine phenolic compounds: 4-hydroxyderricine, 4-hydroxylonchocarpine, 3′,4′,7-trimethoxy-flavonol, 5,4′-dihydroxy-isolonchocarpine, 4-hydroxyderricidine, derricidine, 3,5,4′-trimethoxy-stilbene, 3′,4′,7-trimethoxyflavone and yangambin. The only active extract was a CH2Cl2 root showing minimal inhibitory concentration 800 μg/ml against C. gattii, and the investigation of compounds obtained from this extract showed that 4-hydroxylonchocarpine was active against all three fungi (C. neoformans, C. gattii and C. albicans). These results suggest that D. duckeana extracts have potential therapeutic value for the treatment of pathogenic fungi. © 2018 Sociedade Brasileira de Farmacognosiaen
dc.language.isoenpt_BR
dc.relation.ispartofVolume 28, Número 6, Pags. 697-702pt_BR
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 Brazil*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/br/*
dc.subject3,4 Methylenedioxy 7 Methoxyflavoneen
dc.subject3,4,7 Trimethoxy Flavonolen
dc.subject3,4,7 Trimethoxyflavoneen
dc.subject3,5,4 Trimethoxy 4 Prenylstilbeneen
dc.subject3,5,4 Trimethoxy Stilbeneen
dc.subject4 Hydroxyderricidineen
dc.subject4 Hydroxyderricineen
dc.subject4 Hydroxylonchocarpineen
dc.subject5,4 Dihydroxy Isolonchocarpineen
dc.subjectChalcone Derivativeen
dc.subjectDeguelia Duckeana Extracten
dc.subjectDerricidineen
dc.subjectFlavone Derivativeen
dc.subjectFlavonoiden
dc.subjectPlant Extracten
dc.subjectPlant Medicinal Producten
dc.subjectUnclassified Drugen
dc.subjectYangambinen
dc.subjectAnti-fungal Activityen
dc.subjectCarbon Nuclear Magnetic Resonanceen
dc.subjectCryptococcus Gattiien
dc.subjectCryptococcus Neoformansen
dc.subjectCytotoxicityen
dc.subjectDeguelia Duckeanaen
dc.subjectLiquid Chromatography-mass Spectrometryen
dc.subjectMinimum Inhibitory Concentrationen
dc.subjectNonhumanen
dc.subjectPhytochemistryen
dc.subjectProton Nuclear Magnetic Resonanceen
dc.titleAntifungal activity of extracts and phenolic compounds from Deguelia duckeanaen
dc.typeArtigopt_BR
dc.identifier.doi10.1016/j.bjp.2018.08.004-
dc.publisher.journalBrazilian Journal of Pharmacognosypt_BR
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