CAS 1115-93-1

S-Propyl-L-cysteine

Description:

S-Propyl-L-cysteine is a naturally occurring amino acid derivative characterized by its sulfur-containing side chain. It is a non-essential amino acid, meaning that it can be synthesized by the body. This compound features a propyl group attached to the sulfur atom of the cysteine structure, which contributes to its unique properties. S-Propyl-L-cysteine is known for its potential antioxidant activity, which may help in protecting cells from oxidative stress. Additionally, it plays a role in various biochemical processes, including protein synthesis and metabolism. The presence of the thiol (-SH) group in its structure allows it to participate in redox reactions, making it important in cellular signaling and detoxification pathways. S-Propyl-L-cysteine is also studied for its potential health benefits, including its role in supporting liver function and its implications in various therapeutic applications. As with many amino acids, it is soluble in water and can be involved in peptide formation, contributing to the complexity of biological systems.

Formula: C₆H₁₃NO₂S

InChI: InChI=1S/C6H13NO2S/c1-2-3-10-4-5(7)6(8)9/h5H,2-4,7H2,1H3,(H,8,9)/t5-/m0/s1

InChI key: InChIKey=WAAGBMYUYFBZIW-YFKPBYRVSA-N

SMILES: [C@H](CSCCC)(C(O)=O)N

Synonyms:

• Alanine, 3-(propylthio)-, L-
• L-Cysteine, S-propyl-
• 3-(Propylthio)-L-alanine
• S-(n-Propyl)-L-cysteine
• S-Propyl-L-cysteine