PT-141

FDA Approved

Also known as: Bremelanotide, Vyleesi

Sexual HealthSubcutaneous

A melanocortin receptor agonist FDA-approved for hypoactive sexual desire disorder. Works on the central nervous system rather than the vascular system.

Molecular Weight1025.2 Da
Half-Life (t½)~2.7 hours
SequenceAc-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH

Mechanism of Action

Activates MC3R and MC4R melanocortin receptors in the hypothalamus, stimulating sexual arousal pathways in the CNS.

Dosing Protocol

500-1500 mcg subcutaneous, 45 minutes before activity. Max once per 24 hours, max 8 doses/month.

Open peptide calculator

Reconstitution

10mg vial + 2mL BAC water = 5000 mcg/mL.

Storage

Lyophilized: -20°C. Reconstituted: 2-8°C.

Side Effects

  • Nausea (common)
  • Flushing
  • Headache
  • Skin darkening with repeated use

Key Research Findings

  • FDA-approved as Vyleesi for HSDD in premenopausal women
  • Effective in both male and female arousal in clinical trials
  • CNS-mediated mechanism unlike PDE5 inhibitors

Latest Verified Lab Report

No lab reports available for PT-141 yet.

Community-funded testing results will appear here.

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Research Use Only

This information is provided for educational and research purposes only. It is not intended as medical advice. Always consult a qualified healthcare professional before using any research compounds.