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Melanocortin receptor agonist · 7 aa

Melanotan II

Synthetic cyclic melanocortin receptor agonist analogue of α-MSH

Melanotan II is a synthetic cyclic peptide that acts as a non-selective agonist at melanocortin receptors, developed as an analogue of the naturally occurring hormone alpha-melanocyte-stimulating hormone (alpha-MSH). It has been studied primarily for its ability to stimulate skin pigmentation, and it also produces effects on appetite and sexual arousal through its action on central melanocortin pathways. Despite its widespread gray-market availability, Melanotan II is not an approved or licensed drug in any major jurisdiction. A related derivative, bremelanotide (PT-141), was developed to focus more selectively on the MC4R pathway for sexual function.

Studies tracked
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This page is editorial content summarising reported literature. It does not constitute medical advice and should not be used to guide treatment decisions. Nothing on this page states that any substance cures, treats, or prevents any condition.
Safety first

Side effects & risks

Melanotan II is associated with a substantial and well-documented set of adverse effects, and safety concerns should be weighed carefully before the anecdotal effects. The most commonly reported short-term effects are nausea (sometimes with vomiting), facial flushing, spontaneous erections, decreased appetite, and darkening of existing skin. A specific and serious dermatological concern is that the compound darkens existing moles and can drive the appearance of new or atypical melanocytic nevi; multiple case reports have described changing pigmented lesions in users, and cases have raised concern about melanoma, making the melanoma question an unresolved and important safety signal rather than a settled one. Priapism (a prolonged, painful erection) is a recognized risk and can constitute a medical emergency requiring urgent care. Effects on blood pressure and cardiovascular parameters have also been reported. Because gray-market products are unregulated, there are additional risks of contamination, incorrect dosing, and unsterile injection practices. Melanotan II is not appropriate for people with a personal or family history of melanoma or numerous or atypical moles, and it should not be used without medical oversight. Anyone considering or using it should have baseline and ongoing dermatological monitoring of their skin and moles by a qualified clinician, and any changing lesion should prompt prompt evaluation.

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Latest studies

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Reported protocols (with caveats)

⚠ Editor's caveat
These dose ranges describe what people are reported to do, not what is established as safe or effective. There is no FDA-approved indication. Self-injection of unscheduled peptides carries known and unknown risks. Talk to a clinician.

Melanotan II is described in research and community contexts as a research-use-only compound, not an approved therapy, and any use falls outside regulatory approval. Reported community practice typically distinguishes a loading phase, in which smaller doses are administered daily to build up pigmentation, from a lower-frequency maintenance phase intended to sustain it. The reported route is almost always subcutaneous injection, and reported doses are commonly titrated upward gradually to gauge individual tolerance to nausea and flushing. Some community reports pair use with controlled ultraviolet exposure to develop pigment, while others describe on-demand use for its reported effects on sexual arousal. These patterns reflect anecdotal convention rather than any established or recommended dosing standard, and no regulatory or clinical body endorses them. Because gray-market products vary in concentration and purity, reported doses cannot be assumed to correspond to the actual amount delivered.