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dc.contributor.authorGeris, Regina-
dc.contributor.authorSilva, Ionizete Garcia da-
dc.contributor.authorSilva, Heloísa Helena Garcia da-
dc.contributor.authorBarison, Andersson-
dc.contributor.authorRodrigues-Filho, Edson-
dc.contributor.authorFerreira, Antônio Gilberto-
dc.creatorGeris, Regina-
dc.creatorSilva, Ionizete Garcia da-
dc.creatorSilva, Heloísa Helena Garcia da-
dc.creatorBarison, Andersson-
dc.creatorRodrigues-Filho, Edson-
dc.creatorFerreira, Antônio Gilberto-
dc.date.accessioned2011-08-13T02:18:46Z-
dc.date.available2011-08-13T02:18:46Z-
dc.date.issued2008-
dc.identifier.issn0036-4665-
dc.identifier.urihttp://www.repositorio.ufba.br/ri/handle/ri/2188-
dc.descriptionp.25-28,v.50,n.1,São Paulo Jan./Feb.2008pt_BR
dc.description.abstractThe objective of this study was to evaluate the larvicidal activity of diterpenoids obtained from the oil-resin of Copaifera reticulata against Aedes aegypti larvae, the principal vector of dengue and urban yellow fever. Four diterpenes were obtained from oil-resin extraction with organic solvents and subsequent chromatographic and spectroscopic procedures allowed to isolation and identification of these compounds as 3-b-acetoxylabdan-8(17)-13-dien-15-oic acid (1), alepterolic acid (2), 3-b-hidroxylabdan-8(17)-en-15-oic acid (3), and ent-agatic acid (4). Each compound was previously dissolved in dimethylsulphoxide, and distilled water was added to obtain the desired concentrations. Twenty larvae of third instars were placed into plastic beckers, containing the solution test (25 mL), in a five repetitions scheme, and their mortality, indicated by torpor and darkening of the cephalic capsule, was recorded after 48h. Probit analyses were used to determine lethal concentrations (LC50 and LC90) and their respective 95% confidence intervals. This study showed that only diterpenoids 1 and 2 exhibited larvicidal properties with LC50 of 0.8 ppm and 87.3 ppm, respectively, revealing the former as the most toxic compound against third instars of Ae. aegypti. Therefore, this compound seems to be an interesting source for new metabolite to be exploited.pt_BR
dc.language.isoenpt_BR
dc.subjectCopaifera reticulatapt_BR
dc.subjectent-Labdane Diterpenoidspt_BR
dc.subjectLarvicidal activitypt_BR
dc.subjectAedes aegyptipt_BR
dc.titleDiterpenoids from Copaifera reticulata Ducke with larvicidal activity against Aedes aegypti (L.) (Diptera, Culicidae)pt_BR
dc.title.alternativeRevista do Instituto de Medicina Tropical de São Paulopt_BR
dc.typeArtigo de Periódicopt_BR
dc.description.localpubSão Paulopt_BR
dc.identifier.number50(1):25-28pt_BR
Aparece nas coleções:Artigo Publicado em Periódico (Química)

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