Description
S-Sulforaphaneisasyntheticisothiocyanate.TheRisomerofsulforaphaneisfoundinbroccoli.SulforaphaneisaninducerofphaseIIenzymes,displayingantioxidativeandchemopreventiveactivities.Itmayinhibitthearylhydrocarbonreceptor(AhR).
S-Sulforaphaneisasyntheticisothiocyanate.TheRisomerofsulforaphaneisfoundinbroccoli.SulforaphaneisaninducerofphaseIIenzymes,displayingantioxidativeandchemopreventiveactivities.Itmayinhibitthearylhydrocarbonreceptor(AhR).
Purity | ≥97% |
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Formula | C6H11NOS2 |
FormulaWt. | 177.29 |
ChemicalName | (+)1-Isothiocyanato-4R-(methylsulfinyl)-butane |
IUPACName | 1-isothiocyanato-4-[(S)-methylsulfinyl]butane |
Synonym | D-Sulforaphane |
Solubility | Solubleinethanol,methanol,orethylacetate.MiscIBLewithwaterand/orDMSO. |
Appearance | Slightlyyellowishliquid |
StoreTemp | -20°C |
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ShipTemp | Ambient |
MSDS | S8045MSDSPDF |
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InfoSheet | S8045InfoSheetPDF |
Brochures | SulforaphaneFlyer |
NaturalProductsBooklet |
ABDullRazisAF,HanlonN,SoltysE,etal.ThenaturallyoccurringaliphaticisothiocyanatessulforaphaneanderucinareweakagoNISTsbutpotentnon-competitiveantagonistsofthearylhydrocarbonreceptor.ArchToxicol.2012Oct;86(10):1505-14.PMID:22643862.
AbdullRazisAF,BagattaM,DeNicolaGR,etal.Inductionofepoxidehydrolaseandglucuronosyltransferasebyisothiocyanatesandintactglucosinolatesinprecision-cutratliverslices:importanceofside-chainsubstituentandchirality.ArchToxicol.2011Aug;85(8):919-27.PMID:21132492.