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Melanotan II

✓ Preclinical / Research (parent of approved PT-141)
Melanotan II (MT-II), Non-Selective Melanocortin Agonist
Also known as: MT-II, MT2, Melanotan-2
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Quick Summary

Melanotan II (MT-II) is a synthetic analog of alpha-MSH (alpha-melanocyte-stimulating hormone) that non-selectively activates melanocortin receptors MC1R through MC5R. It produces accelerated skin tanning via MC1R stimulation of melanogenesis, increases libido through MC3R and MC4R activity in the CNS, and suppresses appetite via hypothalamic MC4R.

Skin & Cosmetic Research Use
Melanotan II (MT-II) is a synthetic analog of alpha-MSH (alpha-melanocyte-stimulating hormone) that non-selectively activates melanocortin receptors MC1R through MC5R. It produces accelerated skin tanning via MC1R stimulation of melanogenesis, increases libido through MC3R and MC4R activity in the CNS, and suppresses appetite via hypothalamic MC4R. Unlike Melanotan I (afamelanotide/" class="wiki-internal-link">afamelanotide), which is MC1R-selective, MT-II has broader receptor activity including CNS effects. Bremelanotide (PT-141), an FDA-approved treatment for HSDD - is derived from MT-II.
Storage Stability
Lyophilized
6–12 months (2–8°C)
Reconstituted
~30 days (2–8°C)
Room temp
Avoid

Mechanism of Action

MC1R, Tanning

Activation of MC1R on melanocytes stimulates eumelanin production (dark/brown pigment) and transfer to keratinocytes, producing a tan without UV exposure. Also provides photoprotection by increasing melanin density.

MC4R, Libido & Appetite

Hypothalamic MC4R activation increases dopamine in the mesolimbic system, driving arousal and sexual motivation. The same MC4R pathway reduces food intake, accounting for appetite suppression side effects.

MC3R, Autonomic Effects

MC3R activation contributes to the cardiovascular and autonomic effects (flushing, yawning) often reported at higher doses.

Non-Selectivity Trade-off

MT-II's lack of receptor selectivity gives it broader effects than targeted agents but also more side effects (nausea, spontaneous erections, flushing).

Research Summary

Tanning Efficacy

Multiple studies confirm MT-II produces significant melanin increase (objective colorimetry measurement) within 2–4 weeks of daily dosing, requiring minimal or no UV exposure to achieve tan.

Sexual Function

In men with erectile dysfunction, MT-II produced clinically relevant erections in 80% of subjects in small crossover trials, the data that drove PT-141 development (which removes the tanning effect via its hydroxylated structure).

Appetite Suppression

Animal studies show potent anorexic effects; human reports consistently describe appetite suppression particularly in the first weeks of use.

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Research Protocols

Tanning Protocol

Start at 100–250 µg SubQ to assess tolerance. Progress to 500 µg daily until desired pigmentation achieved, then 2–3x/week maintenance. UV exposure (even brief) amplifies tanning response.

Side Effect Management

Nausea is the most common adverse effect, dose in the evening to sleep through peak nausea window. Yawning, flushing, and spontaneous erections are common at 500 µg+.

Storage & Handling

Store lyophilized" class="wiki-gloss-link">lyophilized at -20°C long-term. Reconstitute with bacteriostatic water. Refrigerate reconstituted solution at 2–8°C; use within 30 days. Protect from light.


References

  • [1]Dorr RT, et al. "Evaluation of Melanotan-II, a superpotent cyclic melanotropic peptide in a pilot phase I clinical study." Life Sci, 1996.
  • [2]Wessells H, et al. "MT-II-induced penile erections in men with psychogenic erectile dysfunction." J Urol, 1998.
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Verified Scientific Data Last audited:
Data Sources & External References
CAS Registry: 121062-08-6  ·  Molecular Formula: C50H69N15O9  ·  Source: peer-reviewed literature  ·  Domain: ascendpeptide.org
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