Melanotan II
Unapproved, and linked to new or changing moles and reported melanoma cases. Sold online as a tanning peptide; regulators in several countries warn against it.
- Evidence
- Limited human research
- Half-life
- Not known
- Sources
- 3 cited
Is melanotan II FDA-approved?
Not approved anywhere. Several countries' regulators have issued warnings about it.
Overview
Melanotan II switches on several melanocortin receptors, so it darkens skin and can cause spontaneous erections and appetite loss. It was tested in small trials in the 1990s, including for erectile dysfunction, and led to bremelanotide (PT-141). Dermatologists have reported new or changing moles and cases of melanoma in users, and health agencies in several countries have warned against it.
How it works
It acts on MC1R (skin pigment), MC3R and MC4R (appetite and sexual function) at once, which is why its effects are broad.
How long does melanotan II stay in the body?
Not well established.
What it's studied for
- Tanning
- Erectile dysfunction (early trials)
Reported side effects
- Nausea, flushing
- New or darkening moles; reported melanoma cases
- Spontaneous erections
- Rare kidney problems (case reports)
Related: Melanotan I (Afamelanotide), PT-141 (Bremelanotide), DSIP, Larazotide.
Sources
The studies and prescribing labels this page is written from.
- Risks of unregulated use of alpha-melanocyte-stimulating hormone analogues: a review. Int J Dermatol, 2017 PubMed
- Melanoma associated with the use of melanotan-II. Dermatology, 2014 PubMed
- Melanotan II User Experience: A Qualitative Study of Online Discussion Forums. Dermatology, 2021 PubMed