Abstract: This study evaluated the antibacterial, antifungal, and antioxidant effect of 7-hydroxy-4’,6-dimethoxy-isoflavone and essential oil of Myroxylon peruiferum. The compound was isolated and its structure elucidated by NMR. The chemical composition of essential oil determined by GC-MS analysis. To evaluation of antimicrobial activity, the Minimum Inhibitory Concentration (MIC), Minimum Bactericidal Concentration (MBC) and Minimum Fungicidal Concentration (MFC) were performed. In addition to analysis of antioxidant activity, DPPH radical scavenging tests, iron chelating assay (FIC), antioxidant reducing power assay (FRAP) and β-carotene bleaching assay (BCB) were performed. For the essential oil were identified 24 organized compounds having as main constituents; Germacrene D (17.2%), α-pinene (14.8%) and E-caryophyllene (10.8%). The results showed that isoflavone (2000 to 156 μg/mL) and essential oil (5.0 to 1.25%) present antibacterial and antifungal activity against Gram-positive bacteria and filamentous fungi. The isoflavone and the essential oil also presented antioxidant activity in all the tests, mainly on inhibition of the oxidation of β-carotene test concentrations ranging from 60 to 100%. In conclusion, isoflavone and essential oil from M. peruiferum present an antimicrobial alternative against Gram-positive bacteria, especially of the genus Staphylococcus and dermatophyte fungi of the genus Trichophyton, as well as a natural compound antioxidant.

In this work, the allantoin was encapsulated with galactomannan extruded from Delonyx regia, by the spray drying technique. The microparticles obtained were structurally characterized by infrared spectroscopy (IR), thermal analysis, scanning electron microscopy (SEM) and the controlled release profile was evaluated. The results of IR suggested the formation of the polymeric wall of the microcapsules and SEM revealed spherical particles with an average size range of 2.84 ± 0.41 µm. X-ray diffraction showed the loss of crystallinity of the active after encapsulation and differential explanatory calorimetry exhibited the loss of its peak melt. The encapsulation efficiency for the microparticles was approximately 84% for the different environmental conditions. The coating of allantoin with the biopolymer promoted a gradual release of the drug over a period of 6 hours and these results are in accordance with the Brazilian Pharmacopoeia. The set of results obtained in this work is relevant and accredits the system developed as a possible alternative for the formation of encapsulated natural drugs destined to possible treatments of cutaneous cellular regeneration.

The chemical investigation of hexane and ethanol extracts from the aerial parts of Vernonia scorpioides resulted in the isolation and characterization of a new polyacetylene lactone, rel-4-dihydro-4β-hydroxy-5a-octa-2,4,6-triynyl-furan-2-(5H)-one, along with the new ethyl 3,4-dihydroxy-6,8,10-triynyl-dodecanoate, and seven known compounds: taraxasteryl acetate, lupeyl acetate, lupeol, lupenone, β-sitosterol, stigmasterol and luteolin. The structure of all compounds was determined by spectrometric techniques (HR-ESI-MS, ¹H and 13C NMR and IV) and comparison with published spectral data.

Dois novos furanoflavonoides, 5-hidróxi-2’’-isopropenil-3-metoxifurano-(2",3":7,8)-flavona e 5-hidróxi-2’’-(1-hidróxi-1-metiletil)-3-metoxifurano-(2",3":7,8)-flavona, juntamente com treze compostos conhecidos, foram isolados das cascas das raízes de Lonchocarpus obtusos (Leguminosae). As estruturas de todos os compostos isolados foram determinadas usando métodos espectrométricos tais como RMN 1D e 2D (COSY, HSQC e HMBC) e EMAR, além da comparação com dados espectrais descritos na literatura para compostos de estruturas semelhantes.

Two new furanoflavonoids, 5-hydroxy-2’’-isopropenyl-3-methoxyfurane-(2",3":7,8)-flavone and 5-hydroxy-2’’-(1-hydroxy-1-methylethyl)-3-methoxyfurane-(2",3":7,8)-flavone, along with thirteen other known compounds, were isolated from the root barks of Lonchocarpus obtusus (Leguminosae). The structures of all compounds were determined by spectrometric methods such as 1D and 2D NMR (COSY, HSQC and HMBC) and HREISMS beside comparison with spectral data for similar compounds.

Croton zehntneri Pax. & K. Hoffm. (Euphorbiaceae) is an aromatic plant native of the northeaster region of Brazil; and is popularly known as "canela de cunhã". The chemical composition of the essential oils from leaves, stalks and roots from three chemotypes of C. zehntneri obtained by hydrodistillation were analyzes by GC-MS. E-anethole, was the main component in the essential oils of all plants parts of che-motype 1. While the phenylpropanoids stragole, eugenol, Z-methyl isoeugenol and E-methyl isoeugenol were the major component in the essential oils of chemotypes 2 and 3, respectively. On TLC the essential oils and the major compounds showed an acetylcholine esterase inhibitory effect.

Croton zehntneri Pax. & K. Hoffm. (Euphorbiaceae) es una planta aromática nativa de la región nororiental de Brasil, y es popularmente conocido como "canela de cunhã". La composición química de los aceites esenciales de hojas, tallos y raíces de três quimiotipos de C. zehntneri obtenido mediante hidrodestilación fueron examinados por GC-MS. E-anetol, fue principal componente en los aceites esenciales de todas las partes de la planta de quimiotipo 1. Si bien la fenilpropanóides estragol, eugenol, Z-metil isoeugenol and E-metil isoeugenol fueron el componente principal en los aceites esenciales de quimiotipos 2 e 3, respectivamente. El TLC estos aceites esenciales y los principales compuestos mostraron una acetilcolina esterase efecto inhibitorio.

The chemical investigation of the hexane and ethanol extracts from aerial parts of Vernonia chalybaea conducted to the isolation and characterization of a new aliphatic tetrahydroxyl ether, along with a series of known compounds such as 4 α,10 α-epoxyaromadendrane, friedelin, taraxasteryl acetate, pseudotaraxasteryl acetate, lupeyl acetate, lupeol, α-amiryn, β-amiryn, β-sitosterol, stigmasterol, 2,3-dimethyl-1,2,3-tri-hydroxybuthanol, angophorol, angophorol-7-O-glucoside, angophorol-7-O-rutinoside, 3,7-dimethoxy-5,3',4'-trihydroxyflavone and acacetin. The structures of all compounds were determined by spectroscopic analysis and comparison with published spectral data.

A composição química dos óleos essenciais das partes aéreas de Pectis apodocephala e Pectis oligocephala foi analisada por CG-EM. Os óleos essenciais destas espécies foram predominantemente constituídos por monoterpenos. Geranial (42, 9-44, 5%), neral (32, 2-34, 2%) e alfa-pineno (10, 7-11, 4%) foram os constituintes majoritários no óleo de P. apodocephala, enquanto p-cimeno (50, 3-70, 9%) e timol (24, 4-44, 7%), foram os compostos prevalentes no óleo de P. oligocephala. Ambos os óleos foram testados contra o nematóide Meloidogyne incognita e larvas do mosquito Aedes aegypti no terceiro estágio. Os resultados obtidos mostraram que os óleos exibem significante atividade e podem, portanto, ser considerados como potenciais agentes nematicida e larvicida naturais.

The chemical composition of the essential oils from aerial parts of Pectis apodocephala and Pectis oligocephala were analyzed by GC-MS. The essential oils of these species were predominantly constituted by monoterpenes. Geranial (42.9-44.5%), neral (32.2-34.2%) and alpha-pinene (10.7-11.4%) were the main constituents in the oil of P. apodocephala, while p-cymene (50.3-70.9%) and thymol (24.4-44.7%), were the prevalent compounds in the oil of P. oligocephala. The essential oils were tested against the root knot nematode Meloidogyne incognita and Aedes aegypti larvae survival. The results obtained show that both essential oils exhibited significant activity and could be considered as potent natural namaticidal and larvicidal agents.

Usando reações clássicas como esterificação e oxidação, uma série de derivados foi obtida a partir da mistura alfa- e beta-amirina, constituintes majoritários da resina de Protium heptaphyllum. Os compostos obtidos foram caracterizados por dados espectroscópicos como: IV, RMN de ¹H e de 13C e comparação com dados da literatura.

Using classic reactions such as esterification and oxidation, a series of derivatives was obtained from the alpha- and beta-amyrin mixture, major compounds of the Protium heptaphyllum resin. The obtained compounds were characterized by spectroscopic data such as: IR, ¹ H and 13C NMR and comparison with literature.

Using high quality epitaxial layers, we have obtained direct evidence of the band inversion in the Pb1-xSn xTe system .The samples, covering the whole composition range, were grown by molecular beam epitaxy on (111)BaF2 substrates. A minimumin the resistivity as a function of temperature was observed for all samples with Sn composition 0.35 <= x <= 0.70. In the same samples and at the same temperature, temperature dependent optical transmission measurements have revealed a change in signal of the energy gap temperature derivative, a direct evidence of the band inversion. However, the temperature for which the inversion occurs is not the one expected by the band inversion model. This discrepancy is supposed to be due to the Burstein-Moss shift caused by the relatively high hole concentration observed in these samples.