MELANOTAN2.XYZ explains one synthetic melanocortin peptide, its chemistry and the rules around it. There is no shop here.
Six copper-coloured spheres joined in a ring with a short tail, linked by dashed lines to labels MC1R, MC3R, MC4R and MC5R on a dark brown hexagonal background
CYCLIC α-MSH ANALOGUE · MC1R · MC3R · MC4R · RESEARCH COMPOUND

Melanotan 2.
One ring, four receptors

Melanotan 2 is a short synthetic peptide folded into a ring. Designed at the University of Arizona in the late 1980s, it switches on most of the body's melanocortin receptors at once, which made it a standard tool in receptor and brain research. This site explains the molecule, its family tree and why regulators keep warning about it.

Melanotan 2 is not approved as a medicine in any country. Research-grade material is a laboratory chemical, and nothing on this site is medical advice.
A lactam-bridged ring of seven residues
Activates four of five melanocortin receptors
No approval as a medicine anywhere

A tool compound with a long shadow

Quick reference

TypeSynthetic cyclic heptapeptide, an analogue of α-MSH
StructureAc-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH2
Formula and massC50H69N15O9, about 1,024 g/mol
Receptor profileAgonist at MC1R, MC3R, MC4R and MC5R; no action at MC2R, the ACTH receptor
OriginUniversity of Arizona, Tucson, described in 1989
Close relativesAfamelanotide (Melanotan 1) and bremelanotide (PT-141), which was derived from it
Regulatory statusNot approved as a medicine in any country; warnings issued by several regulators

A note on purpose

Melanotan2.xyz explains research and regulation. It does not recommend using Melanotan 2, which is a laboratory chemical and not a medicine. If you have a question about your own health, please ask a doctor or pharmacist.

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