Trioxsalen

Trioxsalen

Names
Preferred IUPAC name 2,5,9-Trimethyl-7H-furo[3,2-g][1]benzopyran-7-one
Identifiers
CAS Number	3902-71-4 N
3D model ( JSmol )	Interactive image
ChEBI	CHEBI:28329 Y
ChEMBL	ChEMBL1475 Y
ChemSpider	5383 Y
DrugBank	DB04571 Y
ECHA InfoCard	100.021.327
KEGG	D01034 Y
PubChem CID	5585
UNII	Y6UY8OV51T Y
CompTox Dashboard (EPA)	DTXSID3023716
InChI InChI=1S/C14H12O3/c1-7-4-12(15)17-14-9(3)13-10(6-11(7)14)5-8(2)16-13/h4-6H,1-3H3 Y Key: FMHHVULEAZTJMA-UHFFFAOYSA-N Y InChI=1/C14H12O3/c1-7-4-12(15)17-14-9(3)13-10(6-11(7)14)5-8(2)16-13/h4-6H,1-3H3 Key: FMHHVULEAZTJMA-UHFFFAOYAF
SMILES Cc1cc2c(o1)c(C)c1c(c2)c(C)cc(=O)o1
Properties
Chemical formula	C14H12O3
Molar mass	228.24328
Pharmacology
ATC code	D05AD01 (WHO) D05BA01 (WHO)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). N verify (what is YN ?) Infobox references

Trioxsalen (trimethylpsoralen (TMP), trioxysalen (

Trioxsalen (abbreviated as TMP) activated by UV-A exposure is commonly used in genetics research as an experimental mutagen. UV/TMP generates small deletions (~1-3 Kbp), but all base transitions and transversions can also be obtained.^[5]

References