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Melanotan I

FDA Approved

Also known as: Afamelanotide, CUV1647, Scenesse

Prescription Only — FDA Approved Medication

Educational Content Only

This information is for educational purposes only and does not constitute medical advice, diagnosis, or treatment. The FDA has not evaluated many of the peptides discussed here. Always consult a licensed healthcare provider before making any health decisions.

Overview

Melanotan I (afamelanotide) is a synthetic alpha-melanocyte-stimulating hormone (alpha-MSH) analogue that is FDA-approved (as Scenesse) for the prevention of phototoxicity in adult patients with erythropoietic protoporphyria (EPP). Unlike Melanotan II, it has a more selective pharmacological profile without the erectile and appetite effects seen with non-selective analogues.

Possible Uses

The following areas have been examined in research contexts. This does not constitute medical advice or imply proven efficacy in humans.

  • Skin & Wound Healing
Mechanism of Action

Acts as an agonist at melanocortin 1 receptor (MC1R) on melanocytes, stimulating eumelanin synthesis and increasing skin pigmentation, which reduces phototoxic injury in EPP patients. The selective MC1R profile reduces off-target melanocortin receptor activation.

Safety Notes

FDA-approved (Scenesse) for EPP. Adverse effects include nausea, flushing, and injection site reactions. Changes in pre-existing nevi have been observed and require monitoring. Prescription only.

Research Profile

Half-Life

~15-40 hours (subcutaneous implant formulation)

Administration

subcutaneous implant (approved form)

Legal Status (US)

FDA-approved prescription medication (Scenesse) for EPP.

43 indexed research passages

Categories
Skin & HairImmune & Inflammation
Research Interest Areas
Skin & Wound Healing