Peptide
Melanotan I is an agonist of melanocortin receptors 1, 3, 4, and 5, binding primarily to melanocortin receptor 1 to trigger melanin production.
afamelanotide, afamelanotide acetate, afamelanotide triacetate, Melanotan-1, MT-1, 1566590-77-9, CUV-1647, CUV1647 ACETATE, CHEMBL4297213, A-melanotropin, 4(nle)-7(d-phe), 75921-69-6, Scenesse
Melanotan is a synthetic analogue of alpha-melanocyte-stimulating hormone, or α-MSH for short. α-MSH is one of a number of melanocortin peptide hormones in the body [1]. Melanotan is typically injected or administered as an implant and binds to melanocortin receptors 1, 3, 4, and 5.
There are two types of melanotan molecules: melanotan I and melanotan II. They have both been linked to increased melanin production and increased tanning of the skin [2, 3, 4, 5, 6, 7].
While there is strong research interest in both melanotan molecules, this review will focus on melanotan I.
Melanotan I ([Nle-D-Phe]-α-MSH) is a synthetic peptide that has a linear formation. It is 13 amino acids in length and has the same structure as α-MSH save for two key differences. First, the fourth amino acid in melanotan I is norleucine; second, the seventh amino acid is D-phenylalanine [5].
In the body, melanotan I primarily binds with the MC1R receptor and is more potent and resistant to breakdown than α-MSH [7]. Studies have shown that MT-1 significantly enhances tanning and reduces sunburn [4].
Melanotan I should not be confused with melanotan II (Ac-Nle-[Asp-His-D-Phe-Arg-Trp-Lys]- α-MSH-NH2). MT-2 is less receptor-specific than melanotan I and has been linked to more side effects. Studies have shown that melanotan II increases libido and decreases appetite to a greater extent than MT-1 [6].