Melanotan-2 | Luxbae Peptide Therapy

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Melanocortin Agonist · α-MSH Analogue

Melanotan-2 Tan & Libido Duality

A synthetic α-melanocyte-stimulating hormone analogue with dual pigmentation and central libido effects.

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What Melanotan-2 actually is

Melanotan-2 is a synthetic cyclic heptapeptide analogue of α-melanocyte-stimulating hormone, developed at the University of Arizona in the 1980s.1 It is a non-selective agonist of melanocortin receptors — MC1R (skin pigmentation), MC3R/MC4R (sexual function, appetite). The therapeutic interest is the dual pigmentation and central libido effect that flows from melanocortin engagement.

Unlike afamelanotide (Scenesse, FDA-approved for erythropoietic protoporphyria), Melanotan-2 is not approved for cosmetic use. The related bremelanotide (PT-141) was FDA-approved as Vyleesi for HSDD in 2019 and shares the central libido mechanism.2

At Luxbae, Melanotan-2 is prescribed and supervised by Dr. Ernst von Schwarz, MD, PhD after a complimentary medical consultation.

Mechanism — Melanocortin receptor agonism

Activates MC1R on melanocytes (eumelanin synthesis) and MC3R/MC4R in CNS (appetite suppression, central libido).1

What the research shows

Pigmentation response. Increased melanocyte eumelanin output produces a tanned appearance with less UV exposure than baseline.1

Central libido pathway. MC4R engagement contributes to libido — the same pathway exploited by FDA-approved bremelanotide.2

Appetite modulation. Transient mild appetite suppression consistent with MC4R biology.

Side effects: Nausea (especially first doses), facial flushing, transient BP changes, darkening of existing moles, occasional spontaneous erections in male patients.

FDA note: Not FDA-approved for cosmetic or libido use. PT-141 is FDA-approved for HSDD; afamelanotide is approved for EPP.

Melanotan-2 FAQ

Will it darken my moles?
Often yes. We screen mole burden first; atypical nevi or melanoma history disqualify.

How does it differ from PT-141?
PT-141 targets MC4R primarily and is FDA-approved for libido. Melanotan-2 is non-selective and also acts on MC1R for pigmentation.

References

  1. Dorr RT, Lines R, Levine N, et al. Evaluation of Melanotan-II, a superpotent cyclic melanotropic peptide. Life Sci. 1996;58(20):1777-1784.
  2. Kingsberg SA, Clayton AH, Portman D, et al. Bremelanotide for HSDD. Obstet Gynecol. 2019;134(5):899-908.
  3. Wessells H, Levine N, Hadley ME, et al. Melanocortin receptor agonists, penile erection, and sexual motivation. Int J Impot Res. 2000;12 Suppl 4:S74-79.

Start your Melanotan-2 protocol at Luxbae

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Medical disclaimer: This is educational information, not medical advice. Melanotan-2 is investigational and many uses are not FDA-approved; treatments at Luxbae are administered under medical supervision by Dr. Ernst von Schwarz. Individual results vary.
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