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1.
Chem Biodivers ; 9(8): 1452-64, 2012 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-22899606

RESUMEN

The essential oils (EOs) of two populations of Azorella cryptantha (Clos) Reiche, a native species from San Juan Province, were obtained by hydrodistillation in a Clevenger-type apparatus and characterized by GC-FID and GC/MS analyses. The compounds identified amounted to 92.3 and 88.7% of the total oil composition for A. cryptantha from Bauchaceta (Ac-BAU) and Agua Negra (Ac-AN), respectively. The EO composition for the two populations was similar, although with differences in the identity and content of the main compounds and also in the identity of minor components. The main compounds of the Ac-BAU EO were α-pinene, α-thujene, sabinene, δ-cadinene, δ-cadinol, trans-ß-guaiene, and τ-muurolol, while α-pinene, α-thujene, ß-pinene, γ-cadinene, τ-cadinol, δ-cadinene, τ-muurolol, and a not identified compound were the main constituents of the Ac-AN EO, which also contained 3.0% of oxygenated monoterpenes. The repellent activity on Triatoma infestans nymphs was 100 and 92% for the Ac-AN and Ac-BAU EOs, respectively. Regarding the toxic effects on Ceratitis capitata, the EOs were very active with LD(50) values lower than 11 µg/fly. The dermatophytes Microsporum gypseum, Trichophyton rubrum, and T. mentagrophytes and the bacterial strains Escherichia coli LM(1), E. coli LM(2), and Yersinia enterocolitica PI were more sensitive toward the Ac-AN EO (MIC 125 µg/ml) than toward the Ac-BAU EO. This is the first report on the composition of A. cryptantha EO and its anti-insect and antimicrobial properties.


Asunto(s)
Antiinfecciosos/química , Apiaceae/química , Insecticidas/química , Aceites Volátiles/química , Aceites de Plantas/química , Animales , Antiinfecciosos/aislamiento & purificación , Antiinfecciosos/farmacología , Argentina , Bacterias/efectos de los fármacos , Infecciones Bacterianas/tratamiento farmacológico , Hongos/efectos de los fármacos , Humanos , Insectos/efectos de los fármacos , Insecticidas/aislamiento & purificación , Insecticidas/toxicidad , Micosis/tratamiento farmacológico , Aceites Volátiles/aislamiento & purificación , Aceites Volátiles/farmacología , Aceites de Plantas/aislamiento & purificación , Aceites de Plantas/farmacología
2.
Food Chem Toxicol ; 49(9): 1970-8, 2011 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-21600954

RESUMEN

The chemical profile and botanical origin of Andean Argentinian propolis were studied by HPLC-ESI-MS/MS and GC-MS techniques as well as the antifungal activity according to CLSI protocols. Dermatophytes and yeasts tested were strongly inhibited by propolis extracts (MICs between 31.25 and 125 µg/mL). The main antifungal compounds were: 3'methyl-nordihydroguaiaretic acid (MNDGA) 1, nordihydroguaiaretic acid (NDGA) 2 and a NDGA derivative 3, showing strong activity against Trichophyton mentagrophytes, T. rubrum and Microsporum gypseum (MICs between 15.6 and 31.25 µg/mL). The lignans 1 and 2 showed activities against clinical isolates of Candidas spp., Cryptococcus spp., T. rubrum and T. mentagrophytes (MICs and MFCs between 31.25 and 62.5 µg/mL). The lignan and volatile organic compounds (VOCs) profiles from propolis matched with those of exudates of Larrea nitida providing strong evidences on its botanical origin. These results support that Argentinian Andean propolis are a valuable natural product with potential to improve human health. Six compounds (1-6) were isolated from propolis for the first time, while compounds 1 and 3-6 were reported for first time as constituents of L. nitida Cav.


Asunto(s)
Antifúngicos/farmacología , Cromatografía Líquida de Alta Presión/métodos , Cromatografía de Gases y Espectrometría de Masas/métodos , Larrea/química , Espectrometría de Masas/métodos , Própolis/farmacología , Espectroscopía de Resonancia Magnética , Pruebas de Sensibilidad Microbiana
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