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PT-141 (Bremelanotide)

PT-141 (bremelanotide) is a cyclic heptapeptide melanocortin receptor agonist derived from Melanotan II. It is FDA-approved as Vyleesi for hypoactive sexual desire disorder in premenopausal women. It acts centrally via MC3R and MC4R in the hypothalamus to modulate sexual arousal pathways independent of vascular mechanisms, distinguishing it from PDE5 inhibitors.

Molecular Profile
cyclic
7 AA Sequence
Evidence grade (Strong): Multiple randomized controlled trials in humans. This grade reflects the overall quality of available research on this compound and does not constitute a clinical recommendation.
CAS
189691-06-3
Formula
C50H68N14O10
Chain length
7 aa
Sequence
Ac-Nle-cyclo(Asp-His-D-Phe-Arg-Trp-Lys)-OH
Onset and duration

Acute effect, typically within a few hours of dosing.

Storage and reconstitution

Topical and cosmetic formulations: store per the product directions, typically cool and away from light; follow any beyond-use date.

Clinical Evidence

What the literature says

Scientific Overview

Bremelanotide (Vyleesi) is FDA-approved for premenopausal HSDD. Acts on MC4R in the hypothalamus.

Pharmacokinetics

Half-life (t½)
2.7 h
Approximate plasma half-life
Routes
Subcutaneous

Last reviewed: 2026-05-09

Research Guide

How users approach this compound

The following reflects patterns observed in research literature and community protocols. This is not medical advice and does not constitute a clinical recommendation.

Typical Dose Range Observed

1.75 mg
subcutaneous injection (approved dose)

Research Protocols

Common Dosages

On-Demand

1.0–1.75 mg
≥45 min before activity

Max 1 dose/24h, 8 doses/month

Dosages listed are common research protocols found in peer-reviewed literature and clinical trials. Individual results and requirements may vary significantly in a research context.

Reported Uses

  • FDA-approved for hypoactive sexual desire disorder (HSDD) in premenopausal women (Vyleesi)
  • Studied for male sexual dysfunction in early-stage clinical trials
  • Investigated for appetite regulation via central melanocortin signaling

Key Research Benefits

  • Increases libido
  • Acts on CNS, not vascular
  • Works in both sexes

Potential Side Effects

Nausea
Flushing
BP elevation (transient)
Headache

Considerations and Cautions

  • Contraindicated with cardiovascular disease or uncontrolled hypertension
  • Transient blood pressure increases reported post-dose; require 2 hours monitoring at first use
  • Not approved for use in men or postmenopausal women outside clinical trials

Labs to monitor

Educational context only, not a testing mandate. Any bloodwork decisions belong with your clinician.

  • No validated compound-specific markers: No standard bloodwork is established for this compound; general safety labs (CBC, comprehensive metabolic panel) are reasonable if used under medical supervision.

Dose Calculator

Peptide Reconstitution Calculator

mg

Total amount of peptide in the vial.

mL

Volume of water used to mix.

mcg

Draw to this mark

40 Units

or 0.40 mL on a U-100 syringe

Concentration:2.50 mg/mL
Peptide per Unit:25.00 mcg/unit
*Always double-check your calculations. This tool is for educational purposes only.

PT-141 (Bremelanotide) by goal

Read PT-141 (Bremelanotide)'s profile filtered through specific research goals.

Related Tools

Not medical advice

Information on DoseVault is for educational purposes only and is not a substitute for medical advice, diagnosis, or treatment from a qualified healthcare provider.