Punicafolin
From Infogalactic: the planetary knowledge core
| Chemical structure of punicafolin | |
| Names | |
|---|---|
| Other names
1,2,4-tri-O-galloyl-3,6-(R)-hexahydroxydiphenoyl-β-D-glucose
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| Identifiers | |
| 88847-11-4[1] | |
| ChEMBL | ChEMBL507308 |
| Jmol 3D model | Interactive image |
| PubChem | 5320800 |
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| Properties | |
| C41H30O26 | |
| Molar mass | 938.63 g/mol |
| Vapor pressure | {{{value}}} |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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| Infobox references | |
Punicafolin is an ellagitannin from the leaves of Punica granatum (pomegranate)[1] and in Phyllanthus emblica.[2]
Punicafolin is an isomer of tellimagrandin II and nupharin A, but the hexahydroxydiphenoyl group is not attached to the same hydroxyl groups in the glucose molecule.
Punicafolin has been shown to have tumor suppressive effects in dogs.[3]
References
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Tanimura S et al (2005) Suppression of tumor cell invasiveness by hydrolyzable tannins (plant polyphenols) via the inhibition of matrix metalloproteinase-2/-9 activity. Biochem Biophys Res Commun 330(4):1306-1313
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