Melanotan 2

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Melanotan 2, 10 mg

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Overview

Melanotan II is a synthetic cyclic heptapeptide analog of alpha-melanocyte stimulating hormone (α-MSH), structurally engineered with a cyclic lactam bridge for enhanced metabolic stability and receptor affinity. The compound has been studied in preclinical research as a non-selective melanocortin receptor agonist, with particular research interest in MC1R and MC4R pathway pharmacology (Hruby et al., 1987 — PMID: 3031204).

History

Melanotan II was developed at the University of Arizona in the 1980s through structure-activity optimization research on α-MSH. Early research focused on investigating melanocortin receptor pharmacology and the molecular determinants of receptor selectivity across the MC1-MC5 receptor subtypes. Research has since expanded to include melanocortin pathway studies in metabolic and reproductive models (Dorr et al., 1996).

Structure & Molecular Data

CAS Number 121062-08-6
Molecular Formula C₅₀H₆₉N₁₅O₉
Molecular Weight 1,024.18 g/mol
Amino Acid Count / Structure 7-amino-acid cyclic lactam heptapeptide
PubChem CID 16137315
Sequence Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH₂
Appearance Lyophilized white powder
Storage Store at -20°C. Protect from light and moisture.
Solubility Soluble in sterile water and bacteriostatic water

 

Compound Class & Mechanism

Melanotan II acts as a non-selective agonist at melanocortin receptors (MC1R, MC3R, MC4R, and MC5R), with research documenting affinity across all four receptor subtypes. Melanocortin receptor activation signals primarily through Gs protein-coupled pathways, triggering cAMP accumulation and downstream transcriptional responses in preclinical models.

The compound’s cyclic lactam structure confers enhanced proteolytic resistance and receptor affinity relative to native α-MSH. Research has characterized MT-II activity across multiple pathway contexts including MC1R-mediated melanocyte signaling, MC4R-mediated pathway research in hypothalamic energy homeostasis models, and MC3R/MC4R research in sexual behavior preclinical models (Wessells et al., 2000).

Research Findings

Melanotan II has been investigated in preclinical research spanning melanocortin receptor pharmacology, pigmentation research, metabolic pathway studies, and reproductive behavior research. Published research has documented findings in the following domains:

Key Research Areas

  • Melanocortin Receptor Pharmacology: MC1-MC5 receptor binding profile studies
  • Pigmentation Research: MC1R-mediated melanogenesis research in preclinical models
  • Metabolic Pathway Research: MC4R hypothalamic energy homeostasis research
  • Reproductive Behavior Research: MC3R/MC4R reproductive pathway research in animal models

Collectively, Melanotan II has been established as a foundational research tool for investigating non-selective melanocortin receptor pharmacology and pathway biology across multiple receptor subtypes (Hadley & Dorr, 2006).

Research Context

Researchers study Melanotan II to investigate melanocortin receptor pharmacology, particularly in contexts requiring pan-MC receptor engagement. Its non-selective profile distinguishes it from more selective melanocortin-targeted research compounds.

References

Hruby VJ. et al. (1987). Cyclic lactam alpha-melanotropin analogues of Ac-Nle4-c[Asp5, D-Phe7, Lys10]-alpha-MSH(4-10)-NH2 with bulky aromatic amino acids at position 7 show high antagonist potency and selectivity at specific melanocortin receptors. Journal of Medicinal Chemistry. PMID: 3031204

Dorr RT. et al. (1996). Evaluation of melanotan-II, a superpotent cyclic melanotropic peptide. Annals of the New York Academy of Sciences.

Wessells H. et al. (2000). Melanocortin receptor agonists and male sexual behavior. Peptides.

Hadley ME., Dorr RT. (2006). Melanocortin peptide therapeutics: historical milestones and current status. Peptides.

Ugwu SO. et al. (1997). Skin pigmentation and pharmacokinetics of melanotan-I in humans. Biopharmaceutics & Drug Disposition.

Sawyer TK. et al. (1980). 4-Norleucine, 7-D-phenylalanine-alpha-melanocyte-stimulating hormone: a highly potent alpha-melanotropin with ultralong biological activity. PNAS.

 

REGULATORY & LEGAL NOTICE

Intended Use. This product is sold exclusively as a research chemical for use in controlled laboratory settings by qualified scientific professionals. It is intended solely for in vitro research, analytical standards, and non-clinical preclinical experimentation. The product is not a drug, dietary supplement, cosmetic, food product, or consumer article of any kind.

Prohibited Uses. This product is NOT for use in humans, NOT for veterinary use, NOT for in vivo use in any species, NOT for diagnostic use, NOT for therapeutic use, NOT for food or agricultural use, and NOT for compounding into any preparation intended for administration to humans or animals.

Qualified Professionals Only. Purchasers represent that they are qualified scientific professionals, licensed researchers, or authorized personnel at a research institution, and that this product will be handled in accordance with all applicable institutional, federal, state, and local regulations governing research chemicals.

Regulatory Notice. The statements made regarding this product have not been evaluated by the U.S. Food and Drug Administration. This product has not been approved by the FDA for any therapeutic, diagnostic, or preventive use.

Not a Compounding or Outsourcing Facility. Sirius Molecules is a research chemical supplier. Sirius Molecules is not a compounding pharmacy or outsourcing facility as defined under Sections 503A or 503B of the Federal Food, Drug, and Cosmetic Act.

Legal Compliance. Purchasers are solely responsible for ensuring that their acquisition, possession, handling, and use of this product complies with all applicable laws and regulations in their jurisdiction.

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