Wiki Article
Brevifolin
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| Names | |
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| Preferred IUPAC name
1-(2-Hydroxy-4,6-dimethoxyphenyl)ethan-1-one | |
Other names
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| Identifiers | |
3D model (JSmol)
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.001.799 |
| KEGG | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C10H12O4 | |
| Molar mass | 196.202 g·mol−1 |
| Appearance | solid |
| Melting point | 85-88 °C[1] |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H315, H319, H335 | |
| P261, P264, P264+P265, P271, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Brevifolin or xanthoxylin is a bioactive compound found in pomegranate.[2] The pharmacological profile of brevifolin is reported similar to ellagic acid, particularly with regards to absorption, distribution, and elimination rates.[3]
References
[edit]- ^ PubChem. "Xanthoxylin". pubchem.ncbi.nlm.nih.gov. Retrieved 2025-12-17.
- ^ Hussein, Sahar A.M; Barakat, Heba H; Merfort, Irmgard; Nawwar, Mahmoud A.M (1997). "Tannins from the leaves of Punica granatum". Phytochemistry. 45 (4): 819–823. doi:10.1016/S0031-9422(96)00888-6.
- ^ "Determination and pharmacokinetic study of brevifolin in rat after ig administration of pomegranate leaf extract". Chinese Pharmacological Bulletin. 21 (3): 369–372. 2005.
