CAS 364083-21-6

2-amino-3-(4-methylsulfinylbutylcarbamothioylsulfanyl)propanoic acid

Description:

2-amino-3-(4-methylsulfinylbutylcarbamothioylsulfanyl)propanoic acid, identified by its CAS number 364083-21-6, is a synthetic amino acid derivative characterized by its complex structure, which includes both amino and carboxylic acid functional groups. This compound features a propanoic acid backbone with an amino group at the second carbon and a side chain that incorporates a methylsulfinyl group and a carbamothioylsulfanyl moiety. The presence of sulfur in its structure suggests potential reactivity and interactions typical of thio compounds. Its unique functional groups may impart specific biological activities, making it of interest in pharmaceutical and biochemical research. The compound is likely to be soluble in polar solvents due to the presence of the amino and carboxylic acid groups, while its hydrophobic side chain may influence its overall solubility and interaction with biological membranes. As with many amino acid derivatives, it may play a role in protein synthesis or serve as a building block for more complex molecules in medicinal chemistry.

Formula: C₉H₁₈N₂O₃S₃

InChI: InChI=1/C9H18N2O3S3/c1-17(14)5-3-2-4-11-9(15)16-6-7(10)8(12)13/h7H,2-6,10H2,1H3,(H,11,15)(H,12,13)

SMILES: CS(=O)CCCCN=C(S)SCC(C(=O)O)N

D,L-Sulforaphane-L-cysteine

Controlled Product

CAS: 364083-21-6

Formula: C₉H₁₈N₂O₃S₃

Color and Shape: Light Brown

Molecular weight: 298.45

Ref: TR-S699410

D,L-Sulforaphane-L-cysteine

CAS: 364083-21-6

Sulforaphane is a natural compound found in cruciferous vegetables, such as broccoli, cabbage and cauliflower. It has been shown to inhibit the growth of cancer cells and induce apoptosis in prostate cancer cells. Sulforaphane also induces molecular responses that can be measured in assays, including a decrease in protein expression of cyclin-dependent kinase 2 (CDK2) and an increase in the expression of p21. Sulforaphane has been shown to inhibit cell proliferation by blocking the phosphorylation of retinoblastoma protein (pRB) and reducing the levels of cyclins A2/B1. The optimum concentration for sulforaphane is not yet known, but it has been shown to be more effective at lower concentrations. Sulforaphane has also been shown to reduce tumor size and number in bovine fetuses exposed to carcinogens during gestation. In addition, sulforaphane decreased the incidence of tumors when administered before

Formula: C₉H₁₈N₂O₃S₃

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 298.45 g/mol

Ref: 3D-FS27963

S-(N-Methylsulfinylbutylthiocarbamoyl)-L-cysteine

CAS: 364083-21-6

S-(N-Methylsulfinylbutylthiocarbamoyl)-L-cysteine (SFN-Cys) is an isothiocyanate derivative, functioning as an active metabolite of sulforaphane, a class I and

Formula: C₉H₁₈N₂O₃S₃

Color and Shape: Solid

Molecular weight: 298.45

Ref: TM-T83898