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Melanotan I: Research Overview — Mechanism, Research Areas & References

By the Banger Labs Research Team · Updated June 2026

Melanotan I research peptide

Short answer: Melanotan I (MT-1, afamelanotide) is a synthetic 13-amino-acid analog of α-melanocyte-stimulating hormone (α-MSH) supplied strictly as a research-use-only reference compound for in vitro and preclinical melanocortin-receptor studies. This brief is for informational and laboratory research purposes only and is not a description of any human use, treatment, or outcome.

What is Melanotan I?

Melanotan I is a synthetic linear tridecapeptide structurally based on α-melanocyte-stimulating hormone (α-MSH), with the sequence Ac-Ser-Tyr-Ser-Nle-Glu-His-D-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2. It differs from native α-MSH by two substitutions: norleucine for methionine at position 4 and D-phenylalanine for L-phenylalanine at position 7. These modifications make it more resistant to enzymatic/proteolytic degradation than the native peptide in research models.

Melanotan I — molecular structure (research illustration)

How Melanotan I is studied

In research settings, Melanotan I acts as an agonist at melanocortin receptors, binding with notably high relative affinity at the melanocortin-1 receptor (MC1R) expressed on melanocytes. Receptor activation in preclinical/in vitro systems is reported to stimulate tyrosinase activity and melanogenesis-related pathways. Published comparative work reports the [Nle4, D-Phe7]-α-MSH analog to be substantially more potent than the native α-MSH parent peptide at stimulating melanoma-cell tyrosinase activity in vitro.

Melanotan I — receptor & cell-signaling research illustration

Research areas

  • Studied in melanocortin-1 receptor (MC1R) pharmacology and receptor-binding research models
  • Investigated in in vitro melanogenesis and tyrosinase-activity research
  • Used as a reference α-MSH analog in structure-activity-relationship peptide studies
  • Examined in photoprotection-related preclinical research models
  • Studied for peptide stability/proteolytic-resistance characterization versus the native α-MSH parent peptide

These describe laboratory/preclinical research only. No therapeutic, medical, or efficacy claims are made.

Melanotan I research in a laboratory setting

Melanotan I specifications

Class Synthetic linear tridecapeptide (α-MSH analog)
Form Lyophilized powder (reconstitute with bacteriostatic water)
Purity standard ≥ 99% HPLC
Certificate of Analysis Available per batch on request
Use Research use only — not for human or veterinary use

Handling & quality

Melanotan I is held to a ≥ 99% HPLC purity standard with a Certificate of Analysis available per batch. Reconstitute with bacteriostatic water and store refrigerated; handle strictly for research. See reconstitution & storage.

Melanotan I vial — research-grade detail

Frequently asked questions

What is Melanotan I?

Melanotan I is a synthetic linear tridecapeptide structurally based on α-melanocyte-stimulating hormone (α-MSH), with the sequence Ac-Ser-Tyr-Ser-Nle-Glu-His-D-Phe-Arg-Trp-Gly-Lys-Pro-Val-NH2. It differs from native α-MSH by two substitutions: norleucine for methionine at position 4 and D-phenylalanine for L-phenylalanine at position 7. These modifications make it more resistant to enzymatic/proteolytic degradation than the native peptide in research models.

Is Melanotan I research use only?

Yes. Melanotan I is supplied strictly for laboratory research — not for human or veterinary use, and not as a drug, food, or supplement.

Does Banger Labs provide a COA for Melanotan I?

Yes — a Certificate of Analysis (HPLC purity + mass-spec identity) is available per batch on request. See the COA Library.

References

  1. A review and update on melanocyte stimulating hormone therapy: afamelanotidePubMed (J Drugs Dermatol, 2013)
  2. [Nle4, D-Phe7]-alpha-MSH: a superpotent melanotropin that ‘irreversibly’ activates melanoma tyrosinasePubMed (Endocr Res, 1985)
  3. Afamelanotide for Erythropoietic ProtoporphyriaPMC / NCBI (N Engl J Med, 2015)
  4. AfamelanotideWikipedia (overview, structure/sequence)

Sources are provided for scientific reference and describe laboratory/preclinical research; they do not constitute medical advice or efficacy claims.

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By the Banger Labs Research Team. For research use only. Not for human or veterinary use. Not a drug, food, or cosmetic. Educational information, not medical advice.