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Research Use Policy Summary
For laboratory research use only. Not for human or veterinary consumption, diagnostic use, therapeutic use, or clinical use.

Cognitive & Neuro Research
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Product Usage Notice · This product is intended strictly for research and laboratory use only. It is designated for in vitro testing and experimental purposes. Any use involving human or animal consumption is prohibited by law. All information provided on this website is for educational purposes only. This product must only be handled by licensed, qualified professionals. It is not intended for use as a drug, food, or cosmetic, and must not be misused, mislabeled, or misrepresented as such. Read full Research Use Policy →
Technical specifications
Melanotan-1 (afamelanotide) is a synthetic analog of alpha-MSH containing a D-Phe7 substitution for enhanced melanocortin receptor affinity, studied for melanogenesis and melanocortin receptor signaling.
The Melanocortin-1 Receptor and Human Pigmentation. Annals of the New York Academy of Sciences. Review characterizing MC1R as the primary regulator of human epidermal melanocyte cAMP signaling, tyrosinase activation, and eumelanin synthesis; describes how alpha-MSH and ACTH bind MC1R with comparable affinity and stimulate melanogenesis in primary melanocyte culture models. Cited for in vitro mechanistic context only.
View StudySignificance of the Melanocortin 1 Receptor in Regulating Human Melanocyte Pigmentation, Proliferation, and Survival. Annals of the New York Academy of Sciences. Cell culture study demonstrating that alpha-MSH and ACTH activate MC1R to increase cAMP levels, tyrosinase activity, and melanocyte proliferation in primary human melanocyte cultures; loss-of-function MC1R variants abolished cAMP responses. Cited for in vitro receptor-signaling mechanistic context only.
View StudyThe Melanocortin 1 Receptor and the UV Response of Human Melanocytes — A Shift in Paradigm. Photochemistry and Photobiology. Review summarizing MC1R-mediated cAMP pathway activation, melanocortin-stimulated eumelanin synthesis, and hydrogen peroxide modulation in human melanocyte culture systems; discusses design of potent melanocortin analogues as tool compounds. Cited for preclinical mechanistic context only.
View StudyDefining MC1R Regulation in Human Melanocytes by Its Agonist alpha-Melanocortin and Antagonists Agouti Signaling Protein and beta-Defensin 3. Journal of Investigative Dermatology. Cell-based study characterizing alpha-MSH-induced MC1R activation of adenylate cyclase and tyrosinase in primary human melanocyte cultures, including receptor desensitization kinetics and GRK/beta-arrestin interactions. Cited for in vitro signaling pathway context only.
View StudyThis compound is supplied strictly for in vitro and preclinical research use only. Primary applications include the areas below. MC1R SIGNALING PATHWAY RESEARCH Studied as a tool compound for probing MC1R-coupled Gs protein activation, adenylate cyclase stimulation, and downstream cAMP-PKA pathway dynamics in melanocyte and related cell-based model systems. MELANOGENESIS PATHWAY RESEARCH Investigated in melanocyte culture models for its effects on tyrosinase gene expression, MITF transcription factor pathway modulation, and eumelanin versus pheomelanin synthesis ratio endpoints. MELANOCORTIN RECEPTOR PHARMACOLOGY Used as a reference agonist in binding competition assays and selectivity profiling across melanocortin receptor subtypes (MC1R through MC5R) in recombinant and native expression systems.
Lot records organize identity, purity, storage context, and supporting COA documentation for laboratory intake review.
Lot documentation reports ≥99% purity and identity verification by HPLC and mass spectrometry.
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