
C
Tier
Non-selective melanocortin agonist for tanning and libido.
Peptide, cyclic
WADA Status:
Not listed
Human Trial Scoreboard
Completed human RCTs
Early academic only
Largest Human Study
Size not verified
Longest exposure
Duration not verified
Most Recent Trial
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.