For laboratory research use only. Not for human consumption.

Elite SeriesMelanocortin Research

Melanotan II

Synthetic α-MSH Analog — Cyclic Heptapeptide

Melanotan II is a synthetic cyclic analog of alpha-melanocyte stimulating hormone (α-MSH), originally designed and synthesized at the University of Arizona in the 1980s. Created as a research tool for studying melanocortin receptor activation, it incorporates cyclization and D-amino acid substitutions to increase receptor binding affinity and metabolic stability. It occupies a foundational position in melanocortin research — its broad receptor activity enabled characterization of the MC1R–MC5R receptor family, and its unexpected MC4R-mediated effects led directly to the development of PT-141.

Why Researchers Study It

Melanotan II remains a reference compound in melanocortin research because of its non-selective receptor profile. It activates MC1R through MC5R with varying affinities, making it a valuable tool for studying the entire melanocortin receptor family. The compound illustrates how research tools designed for one purpose can generate discoveries in entirely different biological systems.

Melanocortin Receptor Characterization

Studies have documented Melanotan II's binding affinity across MC1R through MC5R, establishing quantitative dose-response relationships for the melanocortin receptor family.

Melanogenesis Research

Clinical research documented dose-dependent increases in melanin production, establishing the compound's role in MC1R-mediated pigmentation pathway studies.

MC4R-Mediated Pathway Discovery

Unexpected MC4R-mediated effects observed during research directly led to the development of PT-141 and opened an entirely new research direction.

Pharmacokinetic Profiling

Detailed studies have examined absorption, distribution, and metabolism of Melanotan II, providing quantitative bioavailability data that informed future melanocortin peptide design.

Research Timeline

8 milestones spanning 1980–2023

Key Milestones
  • Designed and synthesized as a superpotent cyclic α-MSH analog at University of Arizona (1980–1984)
  • MC4R-mediated effects discovered, directly leading to PT-141 development (1998–2000)
  • Historical milestones review published by Hadley & Dorr in Peptides (2006)

Published Research

Selected citations from the published literature.

Hadley ME, Dorr RT. Melanocortin peptide therapeutics: historical milestones, clinical studies and commercialization. Peptides. 2006;27(4):921-930

Wessells H, et al. Melanocortin receptor agonists, penile erection, and sexual motivation. Int J Impot Res. 2000;12(Suppl 4):S74-S79

Research Use Compliance

All information presented on this page references published preclinical research and is provided for educational and informational purposes only. These products are intended for laboratory research use only. Not for human consumption. No statements on this page have been evaluated by the FDA. This product is not intended to diagnose, treat, cure, or prevent any disease.