S-Allylmercaptocysteine
(2R)-2-amino-3-(prop-2-enyldisulfanyl)propanoic acid
S-Allylmercaptocysteine (SAMC) is a bioactive organosulfur compound primarily derived from garlic (Allium sativum L.). It forms via the reaction between allicin and L-cysteine during garlic processing or metabolism. SAMC features a unique disulfide linkage connecting an allyl moiety to the thiol group of cysteine. Research indicates it exhibits antioxidant, anti-inflammatory, and potential anticancer activities by modulating pathways such as NF-κB, Nrf2, and apoptosis induction in tumor cells. It is more stable than allicin and has been investigated in preclinical models for hepatoprotective and chemopreventive effects. As a cysteine derivative, it participates in thiol-disulfide exchange reactions and may influence cellular redox balance.
Chemical Properties
Volatility
Non-volatile
Does not evaporate readily — minimal aroma contribution
Chemical Behavior
No sensory data available for this chemical component.
