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Skin & Pigmentation

Melanotan II (MT-2)

Cyclic α-MSH analog studied for pigmentation and broad melanocortin receptor activation.

Research use only · U.S. cGMP-aligned sourcing
Melanotan II (MT-2)

Research overview

Melanotan II (MT-2) is a synthetic peptide analogue of the endogenous α-Melanocyte-Stimulating Hormone (α-MSH). Structurally, it is a shorter, cyclic peptide, a modification that distinguishes it from the linear Melanotan I and contributes to its different biological activity profile.

Its mechanism of action involves functioning as a non-selective agonist for the melanocortin receptors. While it potently activates the Melanocortin 1 Receptor (MC1R) to stimulate melanogenesis and cause skin pigmentation, it also strongly binds to other melanocortin receptors, notably the MC3R and MC4R, which are highly expressed in the central nervous system.

This broad receptor engagement results in a wider range of physiological effects than the more selective Melanotan I. In addition to inducing skin tanning, MT-2 is well-documented in research to affect functions regulated by the brain, including increasing libido, suppressing appetite, and influencing metabolism. Its action on these central receptors is also responsible for common side effects such as facial flushing, nausea, and spontaneous erections. MT-2 is an experimental compound that has not been approved for therapeutic use by major regulatory bodies.

Peer-Reviewed Research (PubMed)

Selected landmark / highly-cited studies indexed on PubMed.

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Studied benefits

  • Cyclic α-MSH analog
  • Broad melanocortin receptor activity
  • Stimulates melanogenesis
  • Studied for libido (MC4R) effects
Research notice: Research use only. Typical study ranges: 0.25–0.5 mg subcutaneous. All information is provided strictly for laboratory and educational reference. Not for human consumption. This compound is not approved by the FDA for human or veterinary therapy.
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