Melanotan II (MT-2) is a synthetic cyclic analog of alpha-melanocyte-stimulating hormone (α-MSH) developed at the University of Arizona. It acts on melanocortin receptors MC1R through MC5R, producing a range of effects including skin pigmentation (tanning), sexual arousal, appetite suppression, and potential fat loss.
Originally investigated as a potential sunless tanning agent to reduce melanoma risk, Melanotan II gained widespread underground popularity for its cosmetic tanning effects and sexual function benefits. Its non-selective melanocortin receptor activation is responsible for both its diverse benefits and side effect profile.
While never approved for clinical use, MT-2 remains one of the most widely used cosmetic peptides globally. Its derivative PT-141 (bremelanotide) — which isolated the sexual function pathway — was eventually FDA-approved as Vyleesi for female hypoactive sexual desire disorder.
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