D,L-Sulforaphane

• CAT Number: R002276
• CAS Number: 4478-93-7
• Molecular Formula: C6H11NOS2
• Molecular Weight: 177.30
• Purity: ≥95%
• Synonyms: 1-Isothiocyanato-4-(methylsulfinyl)-butane; 4-Methylsulfinylbutyl Isothiocyanate; ?Sulforaphan
• Target: KEAP1-Nrf2
• Solubility: Soluble in DMSO
• Storage: Store at -20°C
• IUPAC Name: 1-isothiocyanato-4-methylsulfinylbutane
• InChI: InChI=1S/C6H11NOS2/c1-10(8)5-3-2-4-7-6-9/h2-5H2,1H3
• InChIKey: SUVMJBTUFCVSAD-UHFFFAOYSA-N
• SMILES: CS(=O)CCCCN=C=S

D,L-Sulforaphane（Cat No.:R002276）is a bioactive compound derived from cruciferous vegetables, notably broccoli. It is known for its potential chemopreventive properties, acting as an antioxidant and promoting detoxification enzymes. By activating the Nrf2 pathway, D,L-sulforaphane enhances cellular defense mechanisms against oxidative stress and inflammation. Research suggests it may have anticancer effects by inhibiting tumor growth and inducing apoptosis in cancer cells. Additionally, it shows promise in supporting cardiovascular health and neuroprotection. Its diverse biological activities make it a subject of interest in nutritional and pharmaceutical research.

Reference

1: Gamet-Payrastre L. Signaling pathways and intracellular targets of
sulforaphane mediating cell cycle arrest and apoptosis. Curr Cancer Drug Targets.
2006 Mar;6(2):135-45. Review. PubMed PMID: 16529543.

2: Myzak MC, Dashwood RH. Chemoprotection by sulforaphane: keep one eye beyond
Keap1. Cancer Lett. 2006 Feb 28;233(2):208-18. Review. PubMed PMID: 16520150;
PubMed Central PMCID: PMC2276573.

3: Fahey JW, Talalay P. Antioxidant functions of sulforaphane: a potent inducer
of Phase II detoxication enzymes. Food Chem Toxicol. 1999 Sep-Oct;37(9-10):973-9.
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