The N-acetyl derivative of cysteine. It is used as a mucolytic agent to reduce the viscosity of mucous secretions. It has also been shown to have antiviral effects in patients with HIV due to inhibition of viral stimulation by reactive oxygen intermediates. .

Mucomyst - Pharmacology:

Mucomyst may protect against acetaminophen overdose-induced hepatotoxicity by maintaining or restoring hepatic concentrations of glutathione. Glutathione is required to inactivate an intermediate metabolite of acetaminophen that is thought to be hepatotoxic. In acetaminophen overdose, excessive quantities of this metabolite are formed because the primary metabolic (glucuronide and sulfate conjugation) pathways become saturated. Mucomyst may act by reducing the metabolite to the parent compound and/or by providing sulfhydryl for conjugation of the metabolite. Experimental evidence also suggests that a sulfhydryl-containing compound such as acetylcysteine may also directly inactivate the metabolite. Inhalation - Mucomyst exerts its mucolytic action through its free sulfhydryl group, which opens the disulfide bonds and lowers mucus viscosity. This action increases with increasing pH and is most significant at pH 7 to 9. The mucolytic action of acetylcysteine is not affected by the presence of DNA.

Generic name, Overdose, Half Life Mucomyst, Food Interactions, Chemical, etc..

Mucomyst see also

Brand Names containing Acetylcysteine

Chemical structure:
S N O O O H H H H H H H H H C5H9NO3S 2D chemical structure C5H9NO3S SVG | 2D structure S-Acetyl-Cysteine | Acetylcysteine | C5H9NO3S chemical names, chemical properties, classification C5H9NO3S