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PT-141 10mg

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Temperature-Controlled Storage

All peptides maintained at -20C to -22C prior to shipment.

PT-141 10mg

Neurological & Cellular Research

Price Range

£20.99

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Analysis Total

£20.99 GBP

Certificate of Analysis (COA)

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Product Overview

PT-141 (Bremelanotide) is a synthetic cyclic heptapeptide and a non-selective agonist of the melanocortin receptors. Structurally, it is a metabolite of Melanotan II but lacks the C-terminal amide functionality, significantly reducing its affinity for the MC1 receptor (responsible for pigmentation). It is primarily utilised in research to understand the central nervous system's role in physiological arousal pathways.

Mechanism of Research

PT-141 functions via the activation of central melanocortin receptors, specifically MC3R and MC4R, located in the hypothalamus. Unlike vascular-acting agents (such as PDE5 inhibitors), PT-141 modulates dopamine signalling pathways in the brain to influence downstream physiological arousal. Research focuses on its ability to trigger neural excitatory signals independent of the vascular system.

Primary Areas of Investigation

  • Central Nervous System Arousal Pathways
  • Melanocortin Receptor signalling (MC3R/MC4R)
  • Hypothalamic Dopamine Modulation
  • Sexual Dysfunction Models (HSDD/ED)

Product Specifications

Product Name
PT-141 (Bremelanotide)
CAS No.
189691-06-3
Catalogue Number
FP-PT-10
Molecular Formula
C50H68N14O10
Molecular Weight
1025.2 g/mol
Purity
≥ 99.0% (HPLC)
Form
White Lyophilised Powder
Storage
Store lyophilised powder at -20°C for long-term stability; once reconstituted, store refrigerated at 2–8°C.

Disclaimer

This product is sold for in-vitro laboratory research purposes only. It is not a drug, food, or cosmetic and is not intended for human or veterinary consumption. All handling should be performed by qualified professionals in a controlled laboratory setting. Forge Peptides is not liable for any misuse of this product. By purchasing, you agree that you are a qualified researcher or a scientific professional.