Melanotan II
/ Synthetic cyclic heptapeptide analog of alpha-MSH; broad melanocortin receptor agonistALIAS · MT-II · MT-2
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Parent compound of bremelanotide. No FDA approval. Historical academic work; subsequently developed into the approved derivative bremelanotide.
Melanotan II is a synthetic alpha-MSH analog that non-selectively activates melanocortin receptors (MC1R, MC3R, MC4R, MC5R). Activation of MC1R drives eumelanin production (sunless tanning) and activation of MC3R/MC4R influences sexual arousal and appetite pathways.
Academic human work exists (e.g., Wessells 2000 erectile dysfunction study). Not approved as a therapeutic. The derivative bremelanotide was developed to achieve FDA approval with a narrower receptor profile.
Adverse events reported include nausea, flushing, spontaneous erections, blood pressure changes, and focal hyperpigmentation with prolonged use. Reports of melanoma associated with unregulated Melanotan II use exist in the dermatology literature but causality is not established.
Regulatory status
- FDA status:
- Not FDA-approved
Heavily used in the unregulated research-chemical market for “tanning” purposes with no long-term human safety data at recreational doses. Dermatology case reports link unregulated use to melanocytic lesion changes without establishing causation.