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Xanthotoxol information


Xanthotoxol
Chemical structure of xanthotoxol.
Names
IUPAC name
9-Hydroxy-7H-furo[3,2-g][1]benzopyran-7-one
Other names
8-Hydroxypsoralen
8-Hydroxypsoralene
8-Hydroxyfuranocoumarin
Identifiers
CAS Number
  • 2009-24-7
3D model (JSmol)
  • Interactive image
ChemSpider
  • 58600
ECHA InfoCard 100.016.295 Edit this at Wikidata
PubChem CID
  • 65090
UNII
  • 8RL486L8A5 checkY
CompTox Dashboard (EPA)
  • DTXSID50173910 Edit this at Wikidata
InChI
  • 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
SMILES
  • C1=CC(=O)OC2=C(C3=C(C=CO3)C=C21)O
Properties
Chemical formula
C11H6O4
Molar mass 202.16 g/mol
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]

  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

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enzyme psoralen 8-monooxygenase yields xanthotoxol which is followed by a methylation via the enzyme xanthotoxol O-methyltransferase and S-adenosyl methionine...

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similar but different plants. The coumarins osthol, imperatorin and xanthotoxol can be found in C. monnieri. Cnidium monnieri was already described and...

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seeds Dry fruit slices The bael tree contains furocoumarins, including xanthotoxol and the methyl ester of alloimperatorin, as well as flavonoids, rutin...

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C11H6O4

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g/mol, exact mass: 202.0266 u) may refer to: Bergaptol, a furanocoumarin Xanthotoxol, a furanocoumarin This set index page lists chemical structure articles...

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Clausena anisata

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PMID 3395178. Sethi OP, Anand KK, Gulati OD (1992). "Evaluation of xanthotoxol for central nervous system activity". J. Ethnopharmacol. 36 (3): 239–47...

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