Punicafolin
From Wikipedia, the free encyclopedia
| Punicafolin | ||
|---|---|---|
 | ||
| Other names 1,2,4-tri-O-galloyl-3,6-(R)-hexahydroxydiphenoyl-β-D-glucose | ||
| Identifiers | ||
| CAS number | 88847-11-4 | |
| PubChem | 5320800 | |
| ChEMBL | CHEMBL507308 | |
| Jmol-3D images | Image 1 | |
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| Properties | ||
| Molecular formula | C41H30O26 | |
| Molar mass | 938.63 g/mol | |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | ||
| 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
- ↑ Tanaka, T.; Nonaka, G. I.; Nishioka, I. (1985). "Punicafolin, an ellagitannin from the leaves of Punica granatum". Phytochemistry 24 (9): 2075. doi:10.1016/S0031-9422(00)83125-8.
- ↑ Zhang, Y. J.; Abe, T.; Tanaka, T.; Yang, C. R.; Kouno, I. (2001). "Phyllanemblinins A-F, new ellagitannins from Phyllanthus emblica". Journal of natural products 64 (12): 1527–1532. doi:10.1021/np010370g. PMID 11754604.
- ↑ 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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