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Melanotan I

Melanotan I (afamelanotide) is a synthetic analog of α-melanocyte stimulating hormone that selectively targets MC1 receptors to stimulate melanin production.

Melanotan I molecular structure

Overview

Melanotan I (afamelanotide) is a synthetic analog of α-melanocyte stimulating hormone that selectively targets MC1 receptors to stimulate melanin production. While an FDA-approved implant version (SCENESSE®) exists for rare medical conditions, research-grade injectable Melanotan I is studied for its photoprotective and tanning effects through regular subcutaneous administration.

Last reviewed: 2026-08-18

Identity & Aliases

Also known as

Melanotan IAfamelanotide (approved pharmaceutical form)Scenesse (brand)[Nle4-D-Phe7]-α-MSHNDP-MSHMT-1

Status: Research peptide - not approved for human consumption; FDA-approved SCENESSE® implant exists for rare conditions

Full composition (formula, molecular weight, sequence) in Quick Facts →

Research Areas

Erythropoietic protoporphyria (EPP)Photoprotection / pain-free light exposureMelanogenesis via melanocortin-1 receptorCosmetic tanning (unapproved use)

Available Evidence

Human

Afamelanotide (the approved 'melanotan I' analog) is FDA-approved (2019) and EMA-approved for erythropoietic protoporphyria; a placebo-controlled trial (NEJM 2015) showed increased pain-free light exposure and improved quality of life in EPP patients.

Animal

Preclinical models demonstrate MC1R-mediated eumelanin synthesis and photoprotective effects.

In Vitro

In vitro studies show NDP-MSH activation of the melanocortin-1 receptor stimulates melanogenesis in melanocytes.

Uncertain

Use of unregulated 'melanotan' products for cosmetic tanning is not FDA-approved; safety (e.g., changes in nevi, melanoma risk) is not established, and dermatology organizations have warned against unregulated use.

Key Studies & Findings

2 studies
Clinical2019

FDA approved afamelanotide (Scenesse) to increase pain-free light exposure in adults with erythropoietic protoporphyria.

Benefits & Effects

3 documented

Research-grade injectable Melanotan I provides precise dosing control and rapid onset of tanning effects

anecdotal

Unlike the FDA-approved SCENESSE® implant, injectable form allows flexible dosing and can be administered at home

anecdotal

Produces visible tanning within 1-2 weeks with proper UV exposure

anecdotal

No side effects data available yet.

This peptide may have limited safety data.

Limitations & Open Questions

Approved only for EPP; cosmetic tanning use is unapproved and poorly studied; long-term skin cancer risk of melanotan-style products is unknown; the unregulated 'melanotan I/II' sold online is not pharmaceutical grade and varies in purity and dose.

Pharmacology

Synthetic 13-amino-acid analog of α-melanocyte-stimulating hormone (α-MSH), [Nle4-D-Phe7]-α-MSH (NDP-MSH); a potent melanocortin-1 receptor (MC1R) agonist that drives eumelanin production. Afamelanotide is administered as a 16 mg subcutaneous implant with controlled release over approximately 2 months.

Reported Research Dosing

Reported values from research literature and community protocols. Educational reference only — not a dosing recommendation or medical advice.

0.25mg

Route: Injectable
Half-life: ~30 minutes systemic; depot effect days

Research Protocols

Initial Tanning (Light Skin)

Dose
0.25mg
Frequency
2x daily
Route
Subcutaneous injection

Maintenance Tanning

Dose
0.5mg
Frequency
1x daily
Route
Subcutaneous injection

Enhanced Pigmentation

Dose
0.5mg
Frequency
2x daily
Route
Subcutaneous injection

Photoprotection Only

Dose
0.25mg
Frequency
1x daily
Route
Subcutaneous injection

Research protocols are for educational purposes only. Always consult qualified medical professionals.

Frequently Asked Questions

Is Melanotan I the same as the FDA-approved drug?

The approved drug Scenesse is afamelanotide, a pharmaceutical form of 'melanotan I' (NDP-MSH), approved only for erythropoietic protoporphyria — not for tanning.

Is melanotan safe for tanning?

Unregulated melanotan use for tanning is not approved; safety data are lacking and dermatology organizations have issued warnings.

Research Citations

1

Safety Profile Assessment (2006)

(2006)

2

MT-I Photoprotection Study (2004)

(2004)

3

Tanning Efficacy Comparison (2003)

(2003)

Related Resources

Quick Facts

Mechanism

Subcutaneous injection delivers Melanotan I directly into systemic circulation with 100% bioavailability. 30-minute half-life requires multiple daily injections for sustained MC1R activation and melanin production.

Safety Information

Research peptide - not approved for human consumption, sold for research purposes only. Start with lower doses to assess individual tolerance and response. Monitor moles and skin changes - perform regular self-examinations. Use proper sterile injection technique to prevent infections. Maintain UV protection despite enhanced tanning - still risk of overexposure.

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