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MC1R is a G-protein-coupled receptor (GPCR) that, upon agonist engagement, activates the Gs/adenylate cyclase pathway, increasing intracellular cAMP and activating PKA-linked signalling cascades that upregulate tyrosinase activity and drive eumelanin synthesis the dark, UV-protective form of melanin

It stimulates growth hormone release by acting on the ghrelin/growth hormone secretagogue receptor (GHS-R) without significantly affecting cortisol, prolactin, or ACTH levels

Glutathione has no biochemical basis and still has no clinical evidence of cellular bioavailability.

The exact dosing schedule should be individualized by the treating physician based on the patients needs

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