MT-2 (Melanotan II)
10mg
MT-2 10mg
New Releases

MT-2 (Melanotan II)

Non-Selective Melanocortin Agonist

$45.00
Third-Party Lab Tested
COA With Every Order
Fast U.S. Shipping
Text Email

What It Is

A synthetic cyclic heptapeptide analog of α-MSH that acts as a non-selective agonist across multiple melanocortin receptors (MC1R, MC3R, MC4R, MC5R). Originally developed at the University of Arizona as a research tool for studying melanocortin-mediated pigmentation pathways.

How It Works

1
MT-2 binds melanocortin receptors (MC1R, MC3R/4R/5R)
2
Melanocyte adenylate cyclase is activated
3
Eumelanin synthesis is upregulated
4
Pigmentation and centrally mediated pathways are studied

What Researchers Study It For

MC1R / melanogenesis pathway studies
Cyclic peptide melanocortin pharmacology
Photoprotection model investigations
Multi-receptor melanocortin signaling research

Common Research Protocols

In published research, MT-2 has been reconstituted with bacteriostatic water and administered subcutaneously at low-microgram-per-kg doses, with literature noting cumulative pigmentation responses over multi-week protocols in animal models.

Community Interest Areas

The dermatology and melanocortin-pharmacology research community has studied MT-2 since the 1980s as the prototype non-selective melanocortin agonist — used to map receptor distribution, melanin biosynthesis, and the broader physiology of MC1R–MC5R. Its non-selective profile is what makes it a valuable comparator against more recently developed selective agonists.

Non-Selective Agonist across MC1R, MC3R, MC4R, and MC5R
Prototype Studied since the 1980s in melanocortin pharmacology

For research purposes only. Not intended for consumption, clinical application, or diagnostic use.