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Sexual Health
Research Chemical

PT-141

Also known as: PT-141, Bremelanotide

A melanocortin receptor agonist FDA-approved (as Vyleesi) for hypoactive sexual desire disorder in premenopausal women. Acts centrally on the brain rather than the vascular system.

Last updated

Mechanism of Action

PT-141 (bremelanotide) is a cyclic heptapeptide analog of alpha-MSH that activates melanocortin receptors, particularly MC4R, in the central nervous system. Unlike PDE5 inhibitors that work on blood flow, it modulates neural pathways governing sexual desire and arousal. This central mechanism allows it to influence libido directly through hypothalamic signaling.

Half-life
Approximately 2-3 hours
Administration Routes
subcutaneous
Research Status
Research Chemical

Reported Benefits

  • Increases sexual desire and arousal via central pathways
  • FDA-approved (as Vyleesi) for HSDD in premenopausal women
  • Works independently of the vascular system
  • Effective in both men and women in research
  • On-demand use rather than daily dosing

Potential Side Effects

  • Nausea (common, sometimes significant)
  • Flushing and headache
  • Transient increase in blood pressure
  • Darkening of skin or gums with repeated use (melanocortin activity)

Common Dosing

The approved product (Vyleesi) is 1.75 mg subcutaneously on demand, at least 45 minutes before activity, no more than once per 24 hours. Stated as labeled dosing.

The dosing information above is aggregated from research literature and anecdotal community reports for educational purposes only. It is not a recommendation, prescription, or medical advice. Peptides are sold as research chemicals only and are not intended for human use.

Contraindications

  • Uncontrolled hypertension or known cardiovascular disease
  • Pregnancy
  • Concurrent use with certain blood-pressure medications (consult literature)
  • The Patient Experience of Premenopausal Women Treated with Bremelanotide for Hypoactive Sexual Desire Disorder: RECONNECT Exit Study Results

    2021

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  • Bremelanotide for the Treatment of Hypoactive Sexual Desire Disorder: Two Randomized Phase 3 Trials

    2019

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  • Long-Term Safety and Efficacy of Bremelanotide for Hypoactive Sexual Desire Disorder

    2019

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  • Bremelanotide: First Approval

    2019

    View
  • The neurobiology of bremelanotide for the treatment of hypoactive sexual desire disorder in premenopausal women

    2022

    View

Viagra (a PDE5 inhibitor) increases blood flow, while PT-141 acts centrally in the brain on melanocortin receptors to influence sexual desire itself. They target different stages of the response.

Because it activates melanocortin receptors, repeated use can cause some skin or gum darkening, similar to the tanning peptides in the same receptor family.

PeptideChat is for educational and research purposes only. Nothing on this site constitutes medical advice. Peptides are sold as research chemicals only and are not intended for human use. These statements have not been evaluated by the FDA and are not intended to diagnose, treat, cure, or prevent any disease. PeptideChat is an independent educational resource — not a pharmacy, compounding, or 503A/503B outsourcing facility — and does not sell products or provide medical advice.