Ouratea and the other genera of the Ochnaceae family are a rich source of flavonoids and biflavonoids. These can be used as chemotaxonomic markers of Ouratea. Some biflavonoids, as well as extracts of the Ouratea species show important biological activities, such as antitumour, antiviral, vasodilation, antimicrobial and DNA topoisomerase inhibition. On the other hand species of this genus are used in folk medicine for gastric distress, dysentery, and diarrhea; as an astringent, a tonic, and for the treatment of inflammation-related diseases. The information collected in this review attempts to summarise the phytochemical and biological activities studied in Ouratea species that may be helpful to guide researches, to undertake further investigation concerning the common properties of Ouratea species and evaluation as a source of active compounds.

O biflavonóide 2",3"-diidroochnaflavona, isolada de espécies de Luxemburgia (Ochanaceae), foi tratada com diazometano e forneceu o éter trimetílico que, em seguida, foi tratado com anidrido acético/piridina obtendo-se um novo derivado, 5-acetil-7,4'-dimetil-flavona-(3'→O-4'")-5"-acetil-7"-metil-flavanona. Fez-se o completo assinalamento dos dados de RMN ¹H e 13C através da análise dos espectros uni- e bidimensionais do derivado.

The biflavonoid 2",3"-dihydroochnaflavone, isolated from the Luxemburgia species (Ochanaceae), was treated with diazomethane to obtain the trimethyl-ether that was treated with pyridine/acetic anhydride to yield a new derivative, 5-acetil-7,4'-dimethyl-flavone-(3'→O-4'")-5"-acetil-7"-methyl-flavanone. The complete ¹H and 13C NMR data assignments of the new derivative were made by the one- and two-dimensional spectral analysis.

Do caule de Laseguea erecta foram isolados o lupeol, a cumarina escopoletina, o lignóide pinoresinol e o glicosil-cardenoídeo, alfa-L-tevetosil-digitoxigenina. As estruturas foram identificadas com o uso de técnicas espectroscópicas de IV, RMN ¹H e 13C, incluindo técnicas especiais 1D e 2D, espectroscopia de massas e comparação com dados da literatura.

From the stem of Laseguea erecta the triterpene lupeol, the cumarine scopoletin, the lignoid pinoresinol and digitoxigenin alpha-L-tevetoside, known as thevetioside, were isolated. The structures were identified by IR, mass, ¹H and 13C NMR spectroscopy, including 1D and 2D techniques, together with comparison with literature data.

Das raízes, galhos e frutos de Simarouba versicolor foram isolados quassinóides (3, 5-7), triterpenóides (8-14), uma mistura de esteróides (15-17), o flavonóide canferol (18) e o derivado esqualênico 11,14-diacetoxi-7,10;15,18-diepóxi-6,19-diidroxi-6, 7, 10.11, 14, 15, 18, 19-octaidroesqualeno (19). Dados espectrais foram usados para caracterização estrutural.

From the roots, stems and fruits of Simarouba versicolor (Simaroubaceae) were isolated quassinoids (3, 5-7), triterpenoids (8-14), a mixture of steroids (15-17), the flavonoid kaempferol (18) and the squalene derivative 11,14-diacetoxy-7,10; 15,18-diepoxy-6,19-dihidroxy-6,7,10,11,14,15,18,19-octahydrosqualene (19). Spectral data were used for structural characterization.