Xanthotoxol (original) (raw)
From Wikipedia, the free encyclopedia
Xanthotoxol
 |
|
|---|---|
| Names | |
| IUPAC name 9-Hydroxy-7_H_-furo[3,2-_g_][1]benzopyran-7-one | |
| Other names8-Hydroxypsoralen8-Hydroxypsoralene8-Hydroxyfuranocoumarin | |
| Identifiers | |
| CAS Number | 2009-24-7 |
| 3D model (JSmol) | Interactive image |
| ChemSpider | 58600 |
| ECHA InfoCard | 100.016.295  |
| PubChem CID | 65090 |
| UNII | 8RL486L8A5  Y |
| CompTox Dashboard (EPA) | DTXSID50173910 |
| InChI InChI=1S/C11H6O4/c12-8-2-1-6-5-7-3-4-14-10(7)9(13)11(6)15-8/h1-5,13HKey: JWVYQQGERKEAHW-UHFFFAOYSA-NInChI=1/C11H6O4/c12-8-2-1-6-5-7-3-4-14-10(7)9(13)11(6)15-8/h1-5,13HKey: 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 |
Chemical compound
Xanthotoxol is a furanocoumarin. It is one of the major active ingredients in Cnidium monnieri.[1]
- Xanthotoxol O-methyltransferase (8-hydroxyfuranocoumarin 8-O-methyltransferase) is an enzyme that uses S-adenosyl methionine and xanthotoxol to produce S-adenosylhomocysteine and O-methylxanthotoxol (xanthotoxin or methoxsalen).
- ^ 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