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These inhibitors reduce endosomal flux by selectively disrupting Munc13-4 binding to STX7 without impairing other Munc13-4 functions, illustrating how targeting proteinprotein interactions enhances specificity

Moreover, selenocysteine residues, that are typically present in the active site of protective antioxidant enzymes, such as glutathione peroxidase (GPx) and thioredoxin reductase (Trx), are also rapidly oxidized by HOSCN [238]

Stronger oxidants could be involved, overwhelming the glutathione system that may be primarily involved in preventing oxidation of protein sulfhydryl groups in the RBC membrane from lysis

doi: 10.3390/antiox12071375