DL-Sulforaphane N-acetyl-L-cysteine

• CAT Number: R005424
• CAS Number: 334829-66-2
• Molecular Formula: C11H20N2O4S3
• Molecular Weight: 340.48
• Purity: ≥95%
• Synonyms: (2R)-2-acetamido-3-(4-methylsulfinylbutylcarbamothioylsulfanyl)propanoic acid
• InChI: InChI=1S/C11H20N2O4S3/c1-8(14)13-9(10(15)16)7-19-11(18)12-5-3-4-6-20(2)17/h9H,3-7H2,1-2H3,(H,12,18)(H,13,14)(H,15,16)/t9-,20?/m0/s1
• InChIKey: IIHBKTCHILXGOT-KMYGYIBBSA-N
• SMILES: CC(=O)NC(CSC(=S)NCCCCS(=O)C)C(=O)O

DL-Sulforaphane N-Acetyl-L-Cysteine (Cat No.: R005424) is a conjugate of sulforaphane and N-acetyl-L-cysteine (NAC), designed to enhance stability and bioavailability in oxidative stress and cancer research. Sulforaphane, a natural isothiocyanate found in cruciferous vegetables, exhibits potent antioxidant, anti-inflammatory, and anticancer properties by activating the Nrf2 pathway. NAC further supports glutathione synthesis and detoxification. This compound is widely used in studies on neuroprotection, detoxification, and chemoprevention, making it a valuable tool in metabolic disease, inflammation, and cancer research.

Reference

[1]. Liu HJ, et al. Sulforaphane-N-Acetyl-Cysteine Induces Autophagy Through Activation of ERK1/2 in U87MG and U373MG Cells. Cell Physiol Biochem. 2018;51(2):528-542.
[Content Brief]

[2]. Dashwood R H, et al. Dietary histone deacetylase inhibitors: from cells to mice to man[C]//Seminars in cancer biology. Academic Press, 2007, 17(5): 363-369.