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Description
[ CrossRef ] [ Google scholar ] [ PubMed ] Campbell JD, McDonough JE, Zeskind JE, Hackett TL, Pechkovsky DV, Brandsma CA, et al
Promoiety A covalently bound, inactive moiety bound to a drug to form a prodrug that provides the desired pharmaceutical properties
Reversible post-translational disulfide modifications of proteins and their subsequent reduction by thiol-disulfide-dependent antioxidant enzymes constitute the most significant mechanism of intracellular redox signaling
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