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PT-141 (10mg)

PT-141 (Bremelanotide) is studied for its neuroendocrine, melanocortin and behavioral pathway interactions.
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PT-141 (10mg)
High-Purity Melanocortin Receptor Agonist for Neuroendocrine and Behavioral Research

PT-141 (Bremelanotide) (10mg) is a research-grade synthetic peptide derived from the melanocortin system, specifically targeting MC3R and MC4R receptors. It has been widely used in studies exploring sexual behavior, motivation, mood regulation, and neuroendocrine signaling.

Product Overview
Unlike melanocyte-stimulating peptides that act peripherally, PT-141 directly targets the central nervous system, providing researchers with a valuable tool to investigate neural pathways related to desire, stress, reward, and energy balance. Its neuroactive profile makes it suitable for modeling complex behavioral and hormonal responses under controlled conditions.

Key Research Attributes:

  • Neuroendocrine Modulation: Investigated for its effects on hypothalamic pathways influencing mood, motivation, and physiological arousal.
  • Melanocortin Receptor Activity: Acts as a potent agonist for MC3R/MC4R receptors, enabling precise modeling of neurochemical signaling cascades.
  • Behavioral and Cognitive Studies: Evaluated in controlled experiments related to performance, reward, and stress adaptation.
  • Metabolic Function Research: Used in preclinical models studying energy homeostasis, appetite regulation, and hormonal interplay.
  • Laboratory Purity & Stability: Lyophilized for extended shelf life, ensuring consistency and reproducibility in experimental data.


Applications in Scientific Research

  • Melanocortin receptor and CNS pathway studies
  • Neuroendocrine and behavioral signaling research
  • Reproductive behavior and libido modulation models
  • Energy balance and appetite regulation studies
  • Dopaminergic and reward system investigations

Format and Storage
Form: Lyophilized powder
Purity: >99%
Storage: Store at -20°C for optimal stability
Reconstitution: Use bacteriostatic water for solution preparation

Disclaimer: PT-141 (Bremelanotide) (10mg) is intended for laboratory research use only. Not for human or veterinary use. All research must comply with applicable laws and institutional guidelines.



Chemical Makeup

Molecular Formula

  • PT-141: C50H68N14O10

Molecular Weight

  • PT-141: 1025.2 g/mol

Sequence

  • PT-141: Ac-Nle-cyclo(Asp-His-D-Phe-Arg-Trp-Lys)-OH

Other Known Titles

  • PT-141: Bremelanotide, Melanotan Derivative, MC4R Agonist Peptide
 

PT-141 (10mg) is provided strictly for laboratory and research purposes. Please review our Terms and Conditions before placing an order.

Purity Percentage 99% Purity
Volume 10MG
Bought This Week 5
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PT-141 Peptide: Research Overview, Mechanisms, and Neuroendocrine Modulation

PT-141 (Bremelanotide) is a synthetic melanocortin receptor agonist extensively studied for its central nervous system activity. Acting primarily on MC3R and MC4R, PT-141 plays a significant role in research focused on sexual behavior, appetite regulation, energy balance, stress response, and neuroendocrine signaling.

  • Melanocortin Receptor Agonists and Neurobehavioral Regulation
    Reviews PT-141’s selective interaction with MC3R and MC4R receptors and its implications for behavioral modulation.
    Read more
  • PT-141 and the Central Melanocortin System
    Explores hypothalamic pathways activated by PT-141 and its neuroendocrine signaling patterns.
    Read more
  • Behavioral and Hormonal Effects of PT-141
    Summarizes research findings on PT-141’s effects on reproductive behavior, hormone modulation, and CNS activity.
    Read more
  • Melanocortin Pathways in Stress and Motivation Research
    Investigates PT-141’s impact on motivational circuits, dopamine-linked behaviors, and neuroendocrine stress regulation.
    Read more
  • Neuroendocrine Applications of MC4R Agonists
    Focuses on PT-141’s receptor binding characteristics and hypothalamic effects across experimental models.
    Read more
  • Energy Balance and Reward Signaling via the Melanocortin System
    Evaluates PT-141’s influence on feeding behavior, caloric regulation, energy expenditure, and dopaminergic reward pathways.
    Read more
  • PT-141 as a Model for Central Peptide Signaling
    Reviews receptor-specific activation patterns, CNS modulation, and neurochemical interactions of PT-141.
    Read more

Disclaimer: PT-141 is supplied strictly for laboratory research use only. It is not intended for human or veterinary administration. All experimental procedures must follow institutional ethics and regulatory guidelines.

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Frequently asked questions

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Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.
Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

Why choose Peptide Centre? circledown

Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

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Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

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Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

What is included with each order? circledown

Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

How can I verify the quality of your products? circledown

Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

How can I verify the quality of your products? circledown

Retatrutide is characterised in preclinical research for its simultaneous affinity for three distinct receptor classes. This tripartite agonist profile differentiates it from earlier dual-agonist analogues and makes it a subject of significant interest in receptor binding and pharmacodynamic research models.

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