Melanotan II
Melanotan II is studied as a cyclic heptapeptide; non-selective melanocortin receptor agonist (alpha-msh analogue) in biochemical and physiological models.
Melanotan II Biological Classification
Investigated within physiological and chemical models.
What is Melanotan II?
Melanotan II is classified as a cyclic heptapeptide; non-selective melanocortin receptor agonist (alpha-msh analogue). A cyclic melanocortin receptor agonist with no approved drug product. It is structurally very close to bremelanotide, differing at the C-terminus.
Why are people interested in it?
Researchers and clinicians study Melanotan II primarily to understand its biological interactions, receptor binding affinity, and potential role within its biochemical class.
Primary Research Categories
- Melanocortin analogues
How does it work in the body?
Melanotan II interacts with specific cellular receptors and metabolic pathways corresponding to its structural classification as a cyclic heptapeptide; non-selective melanocortin receptor agonist (alpha-msh analogue).
Biological Pathway Overview
Melanotan II Receptor & Target Interactions
This compound is evaluated in scientific research for its interactions with target cellular receptors and signaling cascades. Consult the evidence section below for specific peer-reviewed papers.
Target Pathway
Engages specific cellular signaling cascades characteristic of its structural family.
Endocrine/Paracrine Activity
Investigated for its regulatory effects on local tissue synthesis and cellular signaling.
What has actually been demonstrated in humans?
Evidence for Melanotan II is currently derived primarily from laboratory or preclinical models. Consult the published evidence file for specific indexed studies.
Pharmaceutical Reality vs. Unregulated Research Chemicals
Melanotan II is not an FDA-approved medication. Always verify chemical identity and testing documentation before interpreting research literature.
What is still uncertain or unknown?
Controlled human clinical trials evaluating Melanotan II for therapeutic efficacy, safety, and pharmacokinetics are limited or absent in peer-reviewed Western registries.
Companion Resources & Guides
Dosing Reference
Open Melanotan II Dosing ReferenceA pilot Phase I study exists; no approved product. The study's own conclusion was about dose selection for future Phase I work, not therapy.
Therapept separates official product labels, published clinical study interventions, animal research, clinical references, and community-reported ranges — never blended into one number.
Research at a Glance
Open the full evidence file (3 records)3 records in this file
- CLINICAL TRIAL1
- REVIEW1
- REGULATORY1
Publication span: 1996–2026
What Has Actually Been Studied
- FDA table of bulk drug substances nominated for compounding and subsequently withdrawn (FDA compounding communications, 2026) — Regulatory listing.
- Melanocortin peptide therapeutics: historical milestones, clinical studies and commercialization (Peptides, 2006) — Narrative review.
- Evaluation of melanotan-II, a superpotent cyclic melanotropic peptide in a pilot phase-I clinical study (Life Sciences, 1996) — Pilot Phase I study.
What is Still Unknown
What we know
- A 1996 pilot Phase I study explored pigmentation and tolerability in volunteers. No FDA-approved product followed.
- It is the C-terminal amide; bremelanotide is the free-acid analogue and is approved.
- FDA's withdrawn-nomination entry cites case reports of serious adverse events.
Editorial reading of the records below, labelled as Therapept analysis. How records are built
What remains uncertain
- A contemporary controlled safety database. Case reports are a concern list, not an incidence rate.
Preparation and Handling
Lyophilized peptides ship as freeze-dried powders; whatever happens next involves diluents, concentrations and storage conditions that are compound- and product-specific.
United States Regulatory Status
No FDA-approved product
- No approved drug product exists in Drugs@FDA.
- Listed on FDA's table of bulk substances nominated for compounding and withdrawn by the nominator.
- FDA's published entry references case reports of serious adverse events, including melanoma, posterior reversible encephalopathy syndrome, sympathomimetic toxidrome and priapism.
- Not named on the WADA 2026 Prohibited List.
Technical Chemical SpecificationsClick to view CAS, sequence, and molecular formulas
- Molecular weight
- 1024.2 g/mol
- Sequence length
- 43 chars
- CAS number
- 121062-08-6
- PubChem CID
- 92432
- Compound class
- Cyclic heptapeptide; non-selective melanocortin receptor agonist (alpha-MSH analogue)
- Sequence
- Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-NH2
- Molecular formula
- C50H69N15O9
- Molecular weight
- 1024.2 g/mol
- CAS number
- 121062-08-6
- PubChem CID
- 92432
Sources
Last reviewed 3 September 2026 · Compiled by Therapept Editorial · How these records are built
