Xanthotoxol

From Infogalactic: the planetary knowledge core
Jump to: navigation, search
Xanthotoxol
Chemical structure of xanthotoxol.
Names
IUPAC name
9-hydroxyfuro[3,2-g]chromen-7-one
Other names
8-Hydroxypsoralen
8-Hydroxypsoralene
8-Hydroxyfuranocoumarin
Identifiers
2009-24-7
ChemSpider 58600
Jmol 3D model Interactive image
PubChem 65090
  • InChI=1S/C11H6O4/c12-8-2-1-6-5-7-3-4-14-10(7)9(13)11(6)15-8/h1-5,13H
    Key: JWVYQQGERKEAHW-UHFFFAOYSA-N
  • InChI=1/C11H6O4/c12-8-2-1-6-5-7-3-4-14-10(7)9(13)11(6)15-8/h1-5,13H
    Key: JWVYQQGERKEAHW-UHFFFAOYAF
  • C1=CC(=O)OC2=C(C3=C(C=CO3)C=C21)O
Properties
C11H6O4
Molar mass 202.16 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).
Infobox references

Xanthotoxol is a furanocoumarin. It is one of the major active ingredients in Cnidium monnieri.[1]

Metabolism

References

  1. Xanthotoxol exerts neuroprotective effects via suppression of the inflammatory response in a rat model of focal cerebral ischemia. He W, Chen W, Zhou Y, Tian Y and Liao F, Cell Mol Neurobiol., July 2013, volume 33, issue 5, pages 715-722, doi:10.1007/s10571-013-9939-2

<templatestyles src="Asbox/styles.css"></templatestyles>