Melanotan I

Afamelanotide · Scenesse · NDP-MSH

Rank#999
Skin & HairApprovedApprovedPrescriptionSubQ

Popular for:Skin tanning, photoprotection, erythropoietic protoporphyria (EPP)

19

Total Studies

13

Human Studies

Approved

Evidence Level

Approved

FDA Status

Overview

Melanotan I (Afamelanotide) is a synthetic analog of alpha-melanocyte-stimulating hormone (alpha-MSH) that selectively stimulates melanin production. It is FDA-approved under the brand name Scenesse for erythropoietic protoporphyria (EPP), a rare genetic condition causing extreme sun sensitivity.

Unlike Melanotan II, Melanotan I has a cleaner side effect profile — it primarily targets MC1R (the melanocortin-1 receptor responsible for pigmentation) without significant effects on sexual function or appetite. It was developed by the University of Arizona and is the more selective of the two melanocortin tanning peptides.

Mechanism of Action

Melanotan I binds selectively to MC1R receptors on melanocytes in the skin, stimulating eumelanin production (the dark, photoprotective form of melanin). This increases the skin's natural UV protection. Its selectivity for MC1R over MC3R/MC4R distinguishes it from Melanotan II, which activates multiple melanocortin receptor subtypes and produces broader effects including sexual arousal and appetite suppression.

Key Research Benefits

FDA-approved for EPP (Scenesse) — established safety and efficacy
Selective MC1R activation — tanning without sexual side effects
Studied for photoprotection and UV damage prevention
Researched for skin cancer prevention through increased melanin
Cleaner side effect profile compared to Melanotan II

Clinical Evidence Summary

Research Pipeline

Preclinical
Animal
Phase I
Phase II
Phase III
Approved

International Regulatory Status

🇪🇺
EUApproved2019(Scenesse (afamelanotide))

Prevention of phototoxicity in erythropoietic protoporphyria (EPP)

Source
🇺🇸
USAApproved2019(Scenesse (afamelanotide))

Prevention of phototoxicity in erythropoietic protoporphyria (EPP)

Source

19

Total Studies

13

Human Studies

FDA-approved as Scenesse (2019) for EPP. Available by prescription for EPP patients. Research compound for tanning/photoprotection applications.

Key Studies / PubMed References

Insights into Tanning Biology and Tanning Products.

Meta-Analysis

Resnick G, Khajeh-Afzaly M, Yousefian F, et al. · The Journal of clinical and aesthetic dermatology · 2026

PMID: 41890775

A single-centre, prospective, qualitative analysis of knowledge, attitudes and behaviour of sunbed use among patients attending a pigmented lesion clinic in a tertiary referral centre.

Human Study

Lai FY, Quigley C, Murray G, et al. · Skin health and disease · 2025

PMID: 40584950

Recommended Tool Compounds for the Melanocortin Receptor (MCR) G Protein-Coupled Receptors (GPCRs).

Review

Weirath NA, Haskell-Luevano C · ACS pharmacology & translational science · 2024

PMID: 39296259

Effects of the central melanocortin system on feed intake, metabolic hormones and insulin action in the sheep.

Animal Study

Ehrhardt RA, Giesy SL, Hileman SM, et al. · Journal of animal science · 2023

PMID: 38035762

A glimpse into the underground market of melanotan.

Human Study

Callaghan Iii DJ · Dermatology online journal · 2018

PMID: 30142729

Side Effects & Safety

Nausea (most common)
Facial flushing
Headache
Darkening of moles and freckles (monitor existing nevi)
Injection site reactions

Known Interactions

No curated interaction entry is live for Melanotan I yet.

Until the interaction table is fully populated, use the interaction checker and related peptides below to explore adjacent compounds and likely research pairings.

Frequently Asked Questions

Research Disclaimer

This page is for research and educational purposes only. The information presented is based on published scientific literature and does not constitute medical advice, diagnosis, or treatment recommendations. Melanotan I is not approved by the FDA for human therapeutic use. Always consult a qualified healthcare professional before making any health-related decisions. The studies referenced are linked to their original PubMed sources for verification.