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1.
Planta Med ; 82(9-10): 903-9, 2016 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-27135626

RESUMEN

A chemical investigation of the sponge (Porifera) Myxilla incrustans collected from the unique submarine hydrothermal vent site Strytan, North of Iceland, revealed a novel family of closely related N-acyl dopamine glycosides. Three new compounds, myxillin A (1), B (2) and C (3), were isolated and structurally elucidated using several analytical techniques, such as HR-MS, 1D and 2D NMR spectroscopy. Myxillin A (1) and B (2)were shown to be structurally similar, composed of a dopamine moiety, but differ in the acyl chain length and saturation. The myxillin C (3) has a dehydrotyrosine moiety composing the same acyl chain and glycosylation as myxillin B (2). Myxillins A (1) and C (3) were tested for immunomodulating activity in an in vitro dendritic cell model. Dendritic cells matured and stimulated in the presence of myxillin A (1) secreted lower levels of IL-12p40, whilst dendritic cells matured and stimulated in the presence of myxillin C (3) secreted lower levels of IL-10 compared with dendritic cells matured and stimulated in the presence of the solvent alone. These opposing results indicate that the structural differences in the aromatic ring part of the molecules could have an impact on the immunological effects of dendritic cells. These molecules could, therefore, prove to be important in preventing inflammatory diseases on the one hand, and inducing a response to fight tumors and/or pathogens on the other hand. Further studies will be needed to confirm these potential uses.


Asunto(s)
Dopamina/análogos & derivados , Glicósidos/aislamiento & purificación , Respiraderos Hidrotermales , Factores Inmunológicos/aislamiento & purificación , Poríferos/química , Animales , Productos Biológicos , Células Dendríticas/efectos de los fármacos , Dopamina/química , Dopamina/aislamiento & purificación , Dopamina/farmacología , Glicósidos/química , Glicósidos/farmacología , Humanos , Islandia , Factores Inmunológicos/química , Factores Inmunológicos/farmacología , Estructura Molecular
2.
Phytochemistry ; 66(12): 1440-7, 2005 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-15907957

RESUMEN

In a chemosystematic investigation of Digitalideae (Plantaginaceae), the water-soluble part of extracts of two species of Digitalis, two species of Isoplexis, as well as Erinus alpinus and Lafuentea rotundifolia were studied with regard to their content of main carbohydrates, iridoids and caffeoyl phenylethanoid glycosides (CPGs). Digitalis and Isoplexis contained sorbitol, cornoside and a number of other phenylethanoid glycosides including the new tyrosol beta-D-mannopyranoside, sceptroside but were found to lack iridoid glucosides. Erinus contained mainly glucose, the new 8,9-double bond iridoid, erinoside, and a number of known iridoid glucosides including two esters of 6-rhamnopyranosylcatalpol, as well as the CPG poliumoside. Finally, Lafuentea was characterized by the presence of glucose, aucubin and cryptamygin B but apparently lacked CPGs. The chemosystematic significance of the isolated compounds is discussed.


Asunto(s)
Carbohidratos/aislamiento & purificación , Iridoides/aislamiento & purificación , Plantago/química , Plantago/clasificación , Carbohidratos/clasificación , Clasificación , Glicósidos/clasificación , Glicósidos/aislamiento & purificación , Iridoides/clasificación , Estructura Molecular , Extractos Vegetales/aislamiento & purificación , Hojas de la Planta/química , Tallos de la Planta/química
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