Name | diphlorethohydroxycarmalol |
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Synonyms | 7-(3,5-Dihydroxy-phenoxy)-3-(2,4,6-trihydroxy-phenoxy)-dibenzo[1,4]dioxine-1,2,6,8-tetraol |
Description | Diphlorethohydroxycarmalol, a kind of phlorotannin, is an orally active α-glucosidase and α-amylase inhibitor with IC50s of 0.16 mM and 0.53 mM, respectively. Diphlorethohydroxycarmalol has anti-diabetic activities[1]. |
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Related Catalog | |
Target |
IC50: 0.16 mM (α-glucosidase) and 0.53 mM (α-amylase) [1] |
In Vivo | The increase of postprandial blood glucose levels are significantly suppressed in the Diphlorethohydroxycarmalol-administered group than those in the streptozotocin-induced diabetic or normal mice. Moreover, the area under curve (AUC) is significantly reduced via Diphlorethohydroxycarmalol (100 mg/kg; p.o.) administration (2022 versus 2210 mmol x min/lL) in the diabetic mice as well as it delays absorption of dietary carbohydrates[1]. |
References |
Molecular Formula | C24H16O13 |
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Molecular Weight | 512.38 |
Exact Mass | 512.05900 |
PSA | 218.99000 |
LogP | 4.51960 |