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Key distinction from other GHRPs: Ipamorelin is considered the most selective GHSR agonist, with minimal effects on cortisol release (unlike GHRP-6, GHRP-2), prolactin release, and appetite stimulation (less than ghrelin)

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However, under cellular conditions, the concentration (110 mM) of GSH is several folds higher than of hydroperoxides (10100 M), and thus, the velocity ( V max ) of the detoxification of hydroperoxides by seleno-GPxs is practically independent of the concentration of GSH [8, 17, 18]