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It is present in all cells at millimolar concentrations (110 mM)orders of magnitude higher than any other intracellular antioxidant
This selectivity arose from structural optimization: removing the central dipeptide from GHRP-1 and using Aib N-terminal substitution to create a selective pentapeptide
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Similar findings have been reported in previous studies, where several GSTs exhibited more stable states when coupled with GSH [48]
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