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Email: fitnesssuplements1978@gmail.com Signal: +1(707)742-3597 WhatsApp: +1(707)742-3597 WhatsApp: +90546623186 Text/Call: +1(707)742-3597
Email: fitnesssuplements1978@gmail.com Signal: +1(707)742-3597 WhatsApp: +1(707)742-3597 WhatsApp: +90546623186 Text/Call: +1(707)742-3597

PT-141 10mg

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Rated 5 out of 5

$150.00

Product Name PT-141 (Bremelanotide)
Peptide Content 10mg per vial
Purity ≥98% (HPLC Tested)
Appearance White Lyophilized Powder
Molecular Formula C50H68N14O10
Molecular Weight 1025.18 g/mol
CAS Number 189691-06-3
Sequence Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH
Form Lyophilized Powder
Storage Store at 2°C–8°C, protected from light
Grade Research Grade
Intended Use Laboratory Research Only
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Description

PT-141 10mg Peptide (Bremelanotide) – Premium Research Peptide

PT-141, also known as Bremelanotide, is a synthetic melanocortin receptor agonist derived from Melanotan II. Unlike traditional compounds that primarily influence blood flow, PT-141 has been studied for its interaction with melanocortin receptors in the central nervous system, particularly MC3R and MC4R. Researchers have explored its potential role in sexual function, arousal pathways, neuroendocrine signaling, and behavioral science models.

Our PT-141 10mg Peptide is supplied as a lyophilized powder and manufactured to high purity standards for laboratory and scientific research applications.

Key Features

  • 10mg lyophilized PT-141 (Bremelanotide) per vial
  • High-purity research-grade peptide
  • CAS Number: 189691-06-3
  • Molecular Formula: C50H68N14O10
  • Molecular Weight: 1025.18 g/mol
  • Suitable for laboratory and in-vitro research
  • Securely packaged for stability and storage

Research Applications

PT-141 has been investigated in scientific studies involving:

  • Sexual desire and arousal pathways
  • Melanocortin receptor signaling
  • Neuroendocrine regulation
  • Behavioral and motivation research
  • Central nervous system receptor studies
  • Reproductive health research models

Mechanism of Action

PT-141 functions as a melanocortin receptor agonist, with activity primarily associated with MC3R and MC4R receptors located within the central nervous system. Research suggests that activation of these pathways may influence sexual motivation, arousal responses, and related neurochemical signaling mechanisms. Unlike PDE5 inhibitors, PT-141 is studied for its central nervous system activity rather than vascular effects.

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