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mt 2 | 10 vials
Skin & Beauty PeptidesTanning & Libido

MT-2 | 10 vials

Research Grade 10 vials
129,99 

MT-2 (Melanotan II) is a synthetic cyclic heptapeptide analogue of alpha-melanocyte-stimulating hormone (α-MSH), engineered to be significantly more potent than its linear predecessor . It was developed at the University of Arizona in the 1990s as part of research into melanocortin receptor agonists .

Key Specifications:

  • CAS Number: 121062-08-6

  • Molecular Formula: C₅₀H₆₉N₁₅O₉

  • Molecular Weight: ~1024 Da

  • UNII: UPF5CJ93X7

  • Synonyms: MT-II, Melanotan II, [Nle⁴-D-Phe⁷]-α-MSH (cyclic lactam version)

  • Purity: Variable (unregulated market; research grade typically ≥95-98%)

  • Appearance: White lyophilized powder

  • Storage: Store at 2-8°C (refrigerated); protect from light

Mechanism of Action:

MT-2 acts as a non-selective melanocortin receptor agonist, binding to multiple receptor subtypes :

  • MC1R (melanocortin-1 receptor): Located on melanocytes—stimulates eumelanin production, resulting in skin darkening independent of UV exposure

  • MC3R/MC4R (melanocortin-3 and -4 receptors): Located in the central nervous system—modulate appetite, energy homeostasis, and sexual function

The cyclic structure of MT-2 improves stability and potency, allowing lower doses to exert strong effects, but this comes with broader ("pharmacologically noisy") receptor activity .

Research Applications:

Category Applications
Tanning Research UV-independent melanogenesis, photoprotection studies
Sexual Function Erectile dysfunction research (historical clinical trials); increased libido
Neuroregeneration Peripheral nerve regeneration; neuroprotective properties
Metabolic Research Appetite suppression; thermogenesis; energy expenditure

Clinical History:

MT-2 was investigated clinically for erectile dysfunction and showed promise, with Phase I/II trials completed . However, development stalled due to side effects (primarily nausea), and the program was ultimately not commercialized . A derivative, PT-141 (bremelanotide) , was developed from MT-2 and is FDA-approved for hypoactive sexual desire disorder (HSDD) in premenopausal women .

Important Notice:

FOR RESEARCH USE ONLY. NOT FOR HUMAN USE, THERAPEUTIC, OR DIAGNOSTIC APPLICATIONS.

Select Option & Quantity

Key Benefits

  • High purity research compound (>98%)
  • Third-party tested and verified
  • Lyophilized for maximum stability
  • Certificate of analysis available

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