PT-141 (Bremelanotide) – Melanocortin Agonist – 10MG

$45.00

PT-141 (Bremelanotide) is a synthetic, cyclic heptapeptide analog of alpha-Melanocyte Stimulating Hormone (α-MSH). It functions as a potent, non-selective agonist of the melanocortin receptors, primarily targeting MC3R and MC4R within the central nervous system. Our lyophilized PT-141 is HPLC-verified for >99% purity, ensuring precise receptor binding in demanding neuromodulation and behavioral research assays. Strictly for laboratory research and development use only; not for human consumption.

12 in stock

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1 – 3 $45.00
4+ $35.00 22%

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Description

Product Overview In the study of the central nervous system (CNS), isolating specific receptor pathways is critical. PT-141 is a metabolite of Melanotan II that lacks significant melanogenic (tanning) properties, making it an ideal candidate for isolating and researching the neurological effects of melanocortin system activation.

Mechanism of Action

  • MC4R Agonism: Research indicates PT-141 readily crosses the blood-brain barrier to bind with MC4 receptors, which play a significant role in autonomic nervous system regulation.

  • Non-Vascular Pathway: Unlike compounds that target peripheral blood flow (such as PDE5 inhibitors), PT-141 is studied for its ability to initiate physiological responses directly via central nervous system pathways.

  • Neuromodulation: It is heavily utilized in animal behavioral models to study the neurological triggers of mating behaviors and energy homeostasis.

Quality Assurance

  • Identity: Cyclic Heptapeptide (Melanocortin Agonist)

  • Purity: >99% Verified by HPLC

  • Form: Sterile White Lyophilized Powder

Disclaimer:

WARNING – FOR RESEARCH USE ONLY: This product is sold exclusively as an analytical reference standard and research chemical. It is NOT an FDA-approved drug or medical device. Not for human consumption, therapeutic use, or veterinary application. Any reference to physiological effects is strictly for educational context.