CAS 2281-22-3
:S-Allylmercapto-L-cysteine
Description:
S-Allylmercapto-L-cysteine (CAS 2281-22-3) is a sulfur-containing amino acid derivative that is structurally related to cysteine. It features an allyl group attached to the sulfur atom, which enhances its reactivity and potential biological activity. This compound is known for its antioxidant properties, which can help in scavenging free radicals and reducing oxidative stress in biological systems. S-Allylmercapto-L-cysteine is also recognized for its potential health benefits, including supporting liver function and promoting detoxification processes. In terms of solubility, it is generally soluble in water, which facilitates its absorption and bioavailability in biological systems. The compound is often studied for its role in various biochemical pathways and its potential therapeutic applications, particularly in the context of cardiovascular health and cancer prevention. Overall, S-Allylmercapto-L-cysteine is a compound of interest in both nutritional and pharmaceutical research due to its unique chemical properties and biological effects.
Formula:C6H11NO2S2
InChI:InChI=1S/C6H11NO2S2/c1-2-3-10-11-4-5(7)6(8)9/h2,5H,1,3-4,7H2,(H,8,9)/t5-/m0/s1
InChI key:InChIKey=WYQZZUUUOXNSCS-YFKPBYRVSA-N
SMILES:[C@H](CSSCC=C)(C(O)=O)N
Synonyms:- L-Alanine, 3-(2-propen-1-yldithio)-
- 3-(2-Propen-1-yldithio)-L-alanine
- Alanine, 3-(allyldithio)-, L-
- L-Alanine, 3-(2-propenyldithio)-
- S-Allylmercapto-L-cysteine
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Found 4 products.
S-Allylmercaptocysteine
CAS:<p>S-Allylmercaptocysteine (SAMC) is an organic sulfur compound extracted from garlic with antioxidant activities, protecting against liver cell damage.</p>Formula:C6H11NO2S2Color and Shape:SolidMolecular weight:193.293-(2-Propen-1-yldithio)-L-alanine
CAS:Controlled ProductFormula:C6H11NO2S2Color and Shape:NeatMolecular weight:193.287(2R)-2-Amino-3-(prop-2-en-1-yldisulfanyl)propanoic acid
CAS:<p>(2R)-2-Amino-3-(prop-2-en-1-yldisulfanyl)propanoic acid is an anti-cancer drug that inhibits the enzyme activity of histone deacetylase (HDAC). This drug has been shown to induce apoptosis in colorectal adenocarcinoma cells by inhibiting HDAC. It also induces autophagy and apoptosis in cancer cell lines with different genetic backgrounds. The reaction solution for this compound is a mixture of water, methanol, and hydrochloric acid. The product is soluble in water and methanol, but not in hydrochloric acid.</p>Formula:C6H11NO2S2Purity:Min. 95%Molecular weight:193.3 g/mol




