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Brevifolin

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Brevifolin
Names
Preferred IUPAC name
1-(2-Hydroxy-4,6-dimethoxyphenyl)ethan-1-one
Other names
  • 2-Hydroxy-4,6-dimethoxyacetophenone
  • Phloroacetophenone 2,4-dimethyl ether
  • Xanthoxylin
  • Xanthoxyline
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.001.799 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C10H12O4/c1-6(11)10-8(12)4-7(13-2)5-9(10)14-3/h4-5,12H,1-3H3
    Key: FBUBVLUPUDBFME-UHFFFAOYSA-N
  • InChI=1/C10H12O4/c1-6(11)10-8(12)4-7(13-2)5-9(10)14-3/h4-5,12H,1-3H3
    Key: FBUBVLUPUDBFME-UHFFFAOYAY
  • CC(=O)C1=C(C=C(C=C1OC)OC)O
Properties
C10H12O4
Molar mass 196.202 g·mol−1
Appearance solid
Melting point 85-88 °C[1]
Hazards
GHS labelling:
GHS07: Exclamation mark
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).

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]
  1. ^ PubChem. "Xanthoxylin". pubchem.ncbi.nlm.nih.gov. Retrieved 2025-12-17.
  2. ^ 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.
  3. ^ "Determination and pharmacokinetic study of brevifolin in rat after ig administration of pomegranate leaf extract". Chinese Pharmacological Bulletin. 21 (3): 369–372. 2005.