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1.
Molecules ; 17(12): 14037-45, 2012 Nov 27.
Artículo en Inglés | MEDLINE | ID: mdl-23187287

RESUMEN

Eight compounds were isolated from the water extract of Pu-erh tea and their structures were elucidated by NMR and MS as gallic acid (1), (+)-catechin (2), (−)-epicatechin (3), (−)-epicatechin-3-O-gallate (4), (−)-epigallocatechin-3-O-gallate (5), (−)-epiafzelechin- 3-O-gallate (6), kaempferol (7), and quercetin (8). Their in vitro antioxidant activities were assessed by the DPPH and ABTS scavenging methods with microplate assays. The relative order of DPPH scavenging capacity for these compounds was compound 8 > compound 7 > compound 1 > compound 6 > compound 4 ≈ compound 5 > compound 2 > VC (reference) > compound 3, and that of ABTS scavenging capacity was compound 1 > compound 2 > compound 7 ≈ compound 8 > compound 6 > compound 5 > compound 4 > VC (reference) > compound 3. The results showed that these phenolic compounds contributed to the antioxidant activity of Pu-erh tea.


Asunto(s)
Antioxidantes , Medicamentos Herbarios Chinos , Té/química , Antioxidantes/química , Antioxidantes/aislamiento & purificación , Antioxidantes/farmacología , Benzotiazoles/química , Compuestos de Bifenilo/química , Medicamentos Herbarios Chinos/química , Medicamentos Herbarios Chinos/farmacocinética , Flavonoides/química , Depuradores de Radicales Libres/análisis , Oxidación-Reducción , Fenoles/química , Fenoles/aislamiento & purificación , Fenoles/farmacología , Picratos/química , Ácidos Sulfónicos/química
2.
Molecules ; 16(1): 466-76, 2011 Jan 10.
Artículo en Inglés | MEDLINE | ID: mdl-21221063

RESUMEN

The screening of several Chinese medicinal herbs for insecticidal principles showed that Euphorbia fischeriana roots possessed significant feeding deterrent activity against two stored-product insects (Tribolium castaneum and Sitophilus zeamais). From ethanol extract, four feeding deterrents were isolated by bioassay-guided fractionation. The compounds were identified as jolkinolide B, 12-deoxyphorbol 13-(9Z)-octadecenoate 20-acetate, 17-hydroxyjolkinolide A and B on the basis of their phytochemical and spectral data. Jolkinolide B and 17-hydroxyjolkinolide B possessed strong feeding deterrent activities against S. zeamais (EC50 = 342.1 and 543.9 ppm, respectively) and T. castaneum adults (E50 = 361.4 and 551.5 ppm, respectively). 17-Hydroxyjolkinolide A and 12-deoxyphorbol 13-(9Z)-octadecenoate 20-acetate A also exhibited feeding deterrent activity against the two grain storage insects with EC50 values of 631.9 and 884.3 ppm for S. zeamais and 656.5 and 1058.4 ppm for T. castaneum adults.


Asunto(s)
Escarabajos/fisiología , Diterpenos/farmacología , Euphorbia/parasitología , Conducta Alimentaria/efectos de los fármacos , Plaguicidas/farmacología , Animales , Diterpenos/química , Espectroscopía de Resonancia Magnética , Estructura Molecular , Plaguicidas/química
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