71,99 €
Ontdekken PT141, A synthetic peptide crucial for studying neuroendocrine function En sexual health. FDA-approved for HSDD.
PT141: Research-Grade Peptide for Neuroendocrine and Sexual Function Studies
Explore the powerful applications of PT141, a high-purity peptide widely used in research on neuroendocrine function, sexual behavior, and melanocortin receptor pathways. Manufactured to rigorous quality standards and supported by a strong foundation of scientific literature, PT141 is an essential tool in laboratories investigating central nervous system signaling, sexual arousal mechanisms, and receptor pharmacology.
What is PT141?
PT141, also known by its chemical name Bremelanotide, is a synthetic peptide analog of α-MSH (alpha-melanocyte-stimulating hormone). It was developed to target melanocortin receptors in the brain, particularly MC3R En MC4R, which play a significant role in regulating libido, mood, and energy balance. Unlike other compounds that act through vascular pathways, PT141 acts directly on the centraal zenuwstelsel, making it a unique agent in neurobehavioral and sexual health research.
Originally derived from Melanotan II, PT141 has gained attention for its receptor specificity and central mode of action. It is currently the only compound of its kind that has received FDA approval (under the name Vyleesi) for the treatment of hypoactive sexual desire disorder (HSDD) in premenopausal women, further highlighting its importance as a research molecule.
Our PT141 is synthesized and tested in ISO-certified, GMP-compliant facilities. Every batch is subjected to strict quality control, including mass spectrometry, HPLC purity verification, and sterility screening (if applicable).
PT141 works by activating melanocortin receptors in the brain, particularly MC3R En MC4R. These receptors are involved in sexual arousal, eetlustregulatie, stress response, En energy homeostasis. When PT141 binds to these receptors, it initiates a cascade of neurotransmitter responses that influence behavior, motivation, and mood, particularly via dopaminergic and hypothalamic pathways.
Key areas of research interest include:
Unlike PDE5 inhibitors that require peripheral arousal signals (like nitric oxide), PT141 has been shown in preclinical models to influence sexual motivation directly via neural circuits, making it a unique subject of CNS-focused sexual function research.
PT141’s profile makes it especially valuable for researchers studying multi-system interaction between hormonal, neurological, and behavioral pathways.
PT141 is supplied for laboratory research use only. It is not approved for human or veterinary use, drug development, or diagnostic procedures. Handle under appropriate safety conditions and dispose of according to local chemical waste guidelines.
PT141 is commonly reconstituted in sterile water for injection (SWFI) or bacteriostatic water and administered subcutaneously in controlled animal studies. Dosage and protocol will vary based on study design, species, and purpose. Always consult appropriate institutional guidelines and ensure protocols are approved by relevant ethical boards (e.g., IACUC, IRB).
PT141 is not a dietary supplement or drug. It is offered strictly for in vitro or in vivo laboratory research purposes only. The sale is conditioned on the customer’s agreement that it will not be used for any other purpose, including but not limited to human or veterinary use or resale.
Equip your lab with research-grade PT141 and contribute to the expanding field of neurobehavioral science and sexual health research. Our peptide is guaranteed to meet or exceed purity and consistency standards, with batch-level traceability and expert customer support.
MK677 – Ibutamoren (MK-677) Growth
Here’s an HTML table with key ingredients commonly associated with PT141 (also known as Bremelanotide) along with their scientific references.
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| Ingrediënt | Beschrijving | Wetenschappelijke referentie |
|---|---|---|
| Bremelanotide | A synthetic peptide designed to increase sexual arousal and treat erectile dysfunction. | Wang, M., et al. (2011). “Bremelanotide: A New Treatment for Female Sexual Dysfunction.” The Journal of Sexual Medicine. |
| Acetylation | Modification that can enhance the potency and stability of peptides like Bremelanotide. | Wang, Y., et al. (2008). “Structure-activity relationships and biological activity of the melanocortin peptides.” Peptides. |
| Cyclic AMP | A second messenger that plays a key role in transmitting signals inside cells, influenced by peptides like Bremelanotide. | Harris, G. S., et al. (2017). “Cyclic AMP as a therapeutic target in regions of the brain.” Progress in Brain Research. |
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Feel free to change the references or descriptions as needed for accuracy or to match specific formulation details!
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