| Name | afzelechin |
|---|---|
| Synonyms |
(2R,3R)-2-(4-Hydroxyphenyl)-3,5,7-chromanetriol
(-)-epiafzelechin 2H-1-Benzopyran-3,5,7-triol, 3,4-dihydro-2-(4-hydroxyphenyl)-, (2R,3R)- Afzelechin 2H-1-Benzopyran-3,5,7-triol, 3,4-dihydro-2-(4-hydroxyphenyl)-, (2R,3S)- (2R,3R)-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol epi-Afzelechin 3,5,7,4'-Tetrahydroxyflavan (2R,3S)-2-(4-Hydroxyphenyl)-3,5,7-chromanetriol 2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol |
| Description | (+)-Afzelechin, isolated from rhizomes of Bergenia ligulata, is an alpha-glucosidase activity inhibitor with an ID50 (50% inhibition dose) value of 0.13 mM. (+)-Afzelechin can delay the absorption of carbohydrates in food to suppress postprandial hyperglycemia and hyperinsulinemia[1]. |
|---|---|
| Related Catalog | |
| Target |
ID50: 0.13 mM (alpha-glucosidase)[1] |
| References |
| Density | 1.5±0.1 g/cm3 |
|---|---|
| Boiling Point | 583.4±50.0 °C at 760 mmHg |
| Molecular Formula | C15H14O5 |
| Molecular Weight | 274.269 |
| Flash Point | 306.6±30.1 °C |
| Exact Mass | 274.084137 |
| PSA | 90.15000 |
| LogP | 1.09 |
| Vapour Pressure | 0.0±1.7 mmHg at 25°C |
| Index of Refraction | 1.709 |
| Hazard Codes | Xi |
|---|