glutathione formation The biosynthetic pathway Glutathione in Brain Disorders and

doi:10.1093/jn/130.5.1132 Bendich A, Langseth L

N-Acetyl Amidated versions (NA-Semax Amidate, NA-Selank Amidate) have protective modifications at both ends of the peptide chain that increase stability and bioavailability

Benefits (Research Focus) Redox biochemistry research studied for GSH/GSSG cycling kinetics and cellular thiol-disulfide chemistry Glutathione peroxidase / reductase research investigated as substrate for glutathione-utilizing enzymes in enzyme kinetics studies Phase II conjugation research explored for glutathione S-transferase substrate research and xenobiotic conjugation biochemistry Cellular antioxidant pathway research examined for cellular oxidative stress marker research in cell culture systems -Glutamyl peptide chemistry researched for the unique -linkage SAR properties of natural sulfur-containing peptides What Researchers Look At GSH/GSSG ratio measurements and redox state quantification in cell research models Glutathione peroxidase (GPx) and glutathione reductase (GR) enzyme kinetics studies Glutathione S-transferase (GST) substrate specificity and conjugation chemistry research Cellular thiol redox markers and cysteine pool kinetics Comparative biochemistry versus N-acetylcysteine (NAC) and other thiol-containing research compounds Quick Specs Form: Lyophilized white powder Net Peptide Content: 1500 mg per vial Quantity: 1 vial Appearance: White to off-white lyophilizate Reconstitution: Bacteriostatic or sterile water (added by the end researcher) Purity: 99% by HPLC Identity: MS-verified (per COA) Storage: Protect from light Identity Basics Compound: L-Glutathione (reduced form, GSH) Synonyms: GSH

Motti C, Gnasso A, Bernardini S, et al