C

Tier

Melanotan II

Melanotan II

Melanotan II

Non-selective melanocortin agonist for tanning and libido.

Peptide, cyclic

WADA Status:

Not listed

Human Trial Scoreboard

Completed human RCTs

0
0
0

Early academic only

Largest Human Study

0
0
0

Size not verified

Longest exposure

0
0
0

Duration not verified

Most Recent Trial

0
0
0

Year not verified

Description

Melanotan II is a cyclic peptide that activates melanocortin receptors, which control pigment production in the skin. It emerged from melanocortin research at the University of Arizona, work that also produced an approved medicine in bremelanotide. Melanotan II itself was never developed into a drug and went directly to the grey market as a tanning and libido product. It is the one compound in this database whose grey-market supply has been directly assayed and found wanting: vials labelled as containing ten milligrams were found to hold between four and nine, with unidentified impurities. It has also been the subject of safety warnings from multiple regulators, and it activates receptors involved in far more than pigmentation.

What Are The Claims

Claims made for this compound: Produces UV-independent skin tanning (its most reliable effect); May increase libido via melanocortin activity; Appetite effects reported

Evidence

This entry gets blunt treatment rather than neutral framing, because the published harm record justifies it. The case literature includes melanoma diagnosed in users and eruptive or atypical nevi following use. Cousen and colleagues documented eruptive nevi in a user who also used tanning beds. Ellis and colleagues reported melanoma with a Breslow depth of 1 mm in a 23-year-old. Hjuler and Lorentzen published a melanoma case associated with melanotan II in Dermatology in 2014, and a 2024 report described melanoma in situ diagnosed weeks after use of product from a compounding pharmacy. Systemic toxicity has also been reported, including rhabdomyolysis described by Nelson and colleagues in 2012. Case reports establish association rather than causation, and that distinction should be preserved. But the mechanism is not obscure: this is a non-selective melanocortin agonist that stimulates melanocytes, and melanocytes are the cell of origin for melanoma. Association plus plausible mechanism plus three regulators issuing warnings is about as clear as a signal gets short of a trial nobody will ever run.

Evidence Strength

Preliminary (small human data), safety-flagged

Caveats

Not approved; safety poorly characterized; risks include priapism, nausea, and reports of melanoma/changing moles.

Safety
Alternative Measures
Legal Status

US

Not approved; subject of safety warnings

UK

Not approved; subject of safety warnings

EU

Not approved

AU

Not approved

WADA

Not listed

Not approved in any jurisdiction. Explicitly warned against by the US FDA, the UK MHRA, and the Australian TGA, which has issued repeated consumer alerts and seized product. Sold illegally.

Citations

Hjuler KF, Lorentzen HF (2014). Dermatology. Melanoma associated with melanotan-II. | Cousen P et al. Eruptive nevi following melanotan use. | Ellis R et al. Melanoma in a young melanotan user. | Nelson ME et al. (2012). Rhabdomyolysis associated with melanotan II. | Breindahl T et al. (2015). Drug Testing and Analysis. Product content analysis. PMID: 24771717. | FDA, UK MHRA, and Australian TGA consumer safety warnings.

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