PT-141
Bremelanotide • Vyleesi
Mechanism
Non-selective agonist of melanocortin receptors (MC1, MC3, MC4, MC5). Stimulates libido and sexual function.
Half-Life
2-3 hours
Administration
Technical Protocol
PT-141: Comprehensive Research Guide
Overview
PT-141 (Bremelanotide) is a synthetic peptide analog of α-MSH approved by the FDA for treating sexual dysfunction.
Mechanism of Action
- Activates melanocortin receptors
- Stimulates libido
- Improves sexual function
- Works centrally in the brain
This information is for research and educational purposes only.
Peer-Reviewed Citations
Bremelanotide for the treatment of hypoactive sexual desire disorder
Kingsberg SA, et al. • Obstet Gynecol (2019)
Access ResearchFrequently Asked Questions
What is PT-141?
A synthetic peptide analog of α-MSH approved for treating sexual dysfunction.
How does PT-141 work?
Non-selective agonist of melanocortin receptors (MC1, MC3, MC4, MC5). Stimulates libido and sexual function.
What is the typical dosage of PT-141 in research?
The typical research dosage of PT-141 is 1.75 mg (range: 1-2 mg as needed). Common administration routes include Subcutaneous, Intranasal.
How should PT-141 be stored?
Store at 2-8°C, protect from light
Source PT-141 for Your Research
Third-party tested, EU-shipped, certificate of analysis included. High-purity PT-141 available from our verified research partner.
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