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Melanotan II 10mg research vial

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Melanotan II

Experimental non-selective melanocortin agonist

$54.99In stock10mg
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FOR RESEARCH USE ONLY.Not for human or veterinary use. Not intended to diagnose, treat, cure, or prevent any disease.

Overview

Melanotan II is a cyclic heptapeptide analogue of α-MSH, developed at the University of Arizona alongside melanotan I. A lactam bridge constrains its structure, making it highly potent and resistant to degradation, but also less selective: it activates most melanocortin receptor subtypes rather than MC1R alone.

Small early human studies examined skin pigmentation and, unexpectedly, documented effects on sexual arousal, which led to the development of bremelanotide (PT-141). Melanotan II itself was never approved. Health authorities in several countries have issued warnings about unlicensed products sold online, and dermatology literature includes reports of changes in pigmented lesions. In the laboratory, the peptide remains a widely cited non-selective melanocortin agonist used to probe pigmentation, appetite and central melanocortin signalling. It is supplied here strictly as a research reference compound.

Mechanism studied

  1. Melanotan II
  2. MC1R–MC5R
  3. Melanogenesis
  4. Central MC4R signalling

Melanotan II binds MC1R, MC3R, MC4R and MC5R with high affinity. Activation of MC1R on melanocytes raises cAMP and drives eumelanin synthesis, explaining pigmentation effects. Activation of MC3R and MC4R in the hypothalamus and spinal cord influences appetite, energy expenditure and sexual-function pathways; MC4R agonism is linked to reduced food intake in rodent studies. This broad receptor engagement underlies both its utility as a research tool and the diverse effects reported in early human studies.

Research highlights

  • 01Cyclic lactam α-MSH analogue with high potency and broad receptor activity
  • 02Agonist at MC1R, MC3R, MC4R and MC5R
  • 03Early human pigmentation studies led to the development of bremelanotide
  • 04Not approved anywhere; regulators have issued consumer warnings
  • 05Widely used as a reference ligand in melanocortin and appetite research

Research areas

  • Melanocortin receptor pharmacology
  • Pigmentation models
  • Appetite & MC4R research
  • Sexual-function signalling studies

Evidence & regulatory status

Evidence levelLow
In vitroAnimalHuman trials

Overall status: Not approved — regulatory warnings issued

FDA
Not approved; warnings issued
EMA
Not approved
WADA
Check current list

Key references

  1. [1]PubMed — reviews on melanotan II and dermatological risks
  2. [2]Health alerts — FDA / European agencies

Latest published research

4,562 papers on PubMed →
  1. "Mary thinks that John thinks that…" Developmental change and individual stability in attributing second-order mental states in 5 to 7-year-olds

    Białecka M et al. · Journal of experimental child psychology · 2027 Jan · PMID 42574792

  2. Melatonin testicular synthesis and its role in reproductive physiology in seasonal and non-seasonal breeders

    Cesauri M et al. · Research in veterinary science · 2026 Nov · PMID 42762694

  3. Targeting mitochondrial metabolism in renal cell carcinoma with melatonin: Preclinical evidence and clinical perspectives

    Noroozi-Karimabad M et al. · Tissue & cell · 2026 Nov · PMID 42229285

  4. Neuronal receptor remodeling in the aging periosteum: From single-cell atlases to regenerative targets

    Liu Z et al. · Neural regeneration research · 2026 Oct 29 · PMID 42955884

  5. Maternal piromelatine treatment is associated with attenuated behavioral alterations and sex-specific changes in hippocampal pCREB/BDNF signaling in adult offspring following prenatal constant-light exposure

    Stoyanova T et al. · Behavioural brain research · 2026 Oct 17 · PMID 42892467

  6. HIV-1 Infection Alters Post-Transcriptional Processing of HTLV-1 RNA in MT-2 Cells

    Liu H et al. · Microorganisms · 2026 Oct 15 · PMID 42943598

  7. Anti-HIV-1 activity and mechanism of action of homoplantaginin: A multitarget flavonoid compound

    Liu X et al. · Bioorganic chemistry · 2026 Oct 14 · PMID 42892153

  8. Corrigendum to "RANKL promotes MT2 degradation and ROS production in osteoclast precursors through Beclin1-dependent autophagy" [Differentiation 143, (2025), 100863]

    Ke D et al. · Differentiation; research in biological diversity · 2026 Oct 14 · PMID 42874372

Live feed from PubMed (NCBI) for “Melanotan II”, updated 2026-10-30. Listing a paper is not an endorsement of its findings.

From the public ClinicalTrials.gov registry for “Melanotan II”, updated 2026-10-30. Shown for research context only; Purity Peptides products are not for human use.

FAQ

  • Its cyclic structure binds several melanocortin receptors with high affinity, including MC1R in skin and MC3R and MC4R in the brain. This broad activity makes it a useful pan-agonist reference in receptor studies, but it complicates interpretation when a single receptor pathway is under investigation.

  • Lyophilized Melanotan II is normally kept sealed at −20 °C, protected from light and moisture. Once reconstituted for laboratory work, aliquots are held at 2–8 °C for short-term use or frozen, avoiding repeated freeze–thaw. Follow the lot-specific guidance on the certificate of analysis.

  • Every lot of Melanotan II ships with a certificate of analysis reporting HPLC purity, mass-spectrometry identity against the expected molecular weight, appearance and lot number. Match the COA lot to the vial label and keep it with your experimental records.

Last updated October 2026 · Reviewed by the Purity Peptides research team · Information is a summary of published literature and is not a recommendation for any use.

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