Jump to content

Fraxetin

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Gareth CHEBI (talk | contribs) at 12:42, 19 September 2018 (ChEBI ID added to ChemBox identifiers). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Fraxetin
Chemical structure of fraxetin.
Names
IUPAC name
7,8-dihydroxy-6-methoxychromen-2-one
Other names
7,8-Dihydroxy-6-methoxycoumarin
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.008.525 Edit this at Wikidata
EC Number
  • 209-376-2
KEGG
  • InChI=1S/C10H8O5/c1-14-6-4-5-2-3-7(11)15-10(5)9(13)8(6)12/h2-4,12-13H,1H3
    Key: HAVWRBANWNTOJX-UHFFFAOYSA-N
  • InChI=1/C10H8O5/c1-14-6-4-5-2-3-7(11)15-10(5)9(13)8(6)12/h2-4,12-13H,1H3
    Key: HAVWRBANWNTOJX-UHFFFAOYAM
  • COC1=C(C(=C2C(=C1)C=CC(=O)O2)O)O
Properties
C10H8O5
Molar mass 208.169 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Fraxetin is an O-methylated coumarin. It can be found in Fraxinus rhynchophylla.[1] Fraxin is a glucoside of fraxetin.

References

  1. ^ Thuong, PT; Pokharel, YR; Lee, MY; Kim, SK; Bae, K; Su, ND; Oh, WK; Kang, KW (2009). "Dual anti-oxidative effects of fraxetin isolated from Fraxinus rhinchophylla". Biological & Pharmaceutical Bulletin. 32 (9): 1527–32. doi:10.1248/bpb.32.1527. PMID 19721227.