Información del producto
- [(2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl] 3,4,5-trihydroxybenzoate
- (-)-Epicatechin 3-O-gallate
- (-)-Epicatechin 3-gallate
- (-)-Epicatechol gallate
- (-)-epi-Catechin 3-O-gallate
- (2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate
- (2R,3S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-5-yl 3,4,5-trihydroxybenzoate
- 2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate
- 3-Galloyl-(-)-epicatechin
- 3-Galloyl-(2R,3R)-(-)-Epicatechin
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- 3-O-Galloyl-(-)-epicatechin
- 3-O-Galloylepicatechin
- <span class="text-smallcaps">L</span>-Epicatechin gallate
- Benzoic acid, 3,4,5-trihydroxy-, (2R,3R)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-5,7-dihydroxy-2H-1-benzopyran-3-yl ester
- Benzoic acid, 3,4,5-trihydroxy-, 2-(3,4-dihydroxyphenyl)-3,4-dihydro-5,7-dihydroxy-2H-1-benzopyran-3-yl ester, (2R-cis)-
- ECG
- Epicatechol 3-gallate
- Gallic acid, 3-ester with epicatechol, (-)-
- L-Ecg
Stability Light Sensitive
Applications One of the catechin isomers and a potent antioxidant that can modulate a wide range of membrane proteins. Its bilayer-modifying potency was tested using gramicidin A (gA) channels as probes. All the catechins alter gA channel function and modify bilayer properties, with a 500-fold range in potency. The gallate group causes current block, as evident by brief downward current transitions.
References Ingolfsson, H., et al.: FEBS Lett., 585, 3101 (2011),
Propiedades químicas
Consulta técnica sobre: TR-E582265 (-)-Epicatechin Gallate
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