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Specimen Atlas of Research Peptides30 plates · MIT
← CataloguePlate XVIII of XXX
XVIIIPlate XVIIIFDA approved · 2019Reviewed 2026-04-25

PT-141

Melanocortin-4 Receptor Agonist

also known as Bremelanotide, Vyleesi, PT 141

Cyclic 7-amino-acid peptide and MC4R-selective agonist derived from α-MSH. FDA-approved 2019 (Vyleesi) for hypoactive sexual desire disorder in pre-menopausal women — the first centrally-acting peptide for sexual dysfunction. Acts on hypothalamic melanocortin pathways to drive arousal independent of vascular pathways (unlike PDE5 inhibitors).

§ I

At a glance

Half-life
~2.7 hr
Route

SQ · Abdomen / thigh · ≥45 min before sex

§ II

Mechanism

Primary target — Melanocortin-4 receptor (MC4R) in hypothalamus [simerly-2023][fda-vyleesi-label-2019].

Pathway — MC4R agonism in paraventricular nucleus → autonomic + neuroendocrine sexual arousal pathways [simerly-2023].

Downstream effect — Increased sexual desire and arousal; central rather than peripheral mechanism [clayton-2015].

Origin — Cyclic 7-AA peptide derived from α-MSH (agonist Ac-Nle-Asp-His-D-Phe-Arg-Trp-Lys-OH cyclic) [fda-vyleesi-label-2019].

§ III

Dosage

Protocols described in the cited literature; not medical advice.

ParameterValue
Standard dose1.75 mg SQ [fda-vyleesi-label-2019]Single dose ≥45 min before anticipated sexual activity. Max 1 dose / 24 hr.
FrequencyPRN, max 8 doses / month
Lower / starter dose1 mg (off-label)
Evidence basisFDA-approved (HSDD pre-menopausal women) [fda-vyleesi-label-2019][clayton-2015]
DurationPRN; reassess if no benefit after 8 doses
ReconstitutionPre-filled commercial pen (Vyleesi). Research vial: bacteriostatic water.
Timing≥45 min before sexual activity
Half-life~2.7 hr [fda-vyleesi-label-2019]
§ III · b

Reconstitution

A pure mass-to-volume utility. Enter what you have in the vial; the atlas computes the volume per dose. No prescription information.

Inputs
The calculator does pure mass-to-volume math. It does not recommend a dose. Refer to PT-141's cited literature for protocol specifics.
Volumetric outputFig. C — reconstitution math
Volume per dose
0.286mL
28.6 units on a U-100 insulin syringe
Concentration
875
mcg per mL
Doses per vial
7
at this dose
§ V

Adverse events

Severities follow the FDA / CTCAE convention.

Nauseamoderate
Common (~40%); often transient [fda-vyleesi-label-2019]
Flushingmild
Common, transient
Injection site reactionmild
Erythema, mild pain
Headachemild
Common
Hyperpigmentation (focal)moderate
Rare focal skin darkening; reversible after discontinuation [fda-vyleesi-label-2019]
Hypertension (transient)moderate
Mean ↑6 mmHg systolic peaking ~4 h post-dose; resolves within 12 h [fda-vyleesi-label-2019]
Pregnancy / OBsevere
Contraindicated
Cardiovascular diseasemoderate
Use caution; transient BP rise
Absolute contraindications
  • Uncontrolled hypertension
  • Known cardiovascular disease (caution)
  • Pregnancy
Relative contraindications
  • Pre-existing hyperpigmentation disorders
  • MC4R-pathway-dependent psychiatric conditions
§ VI

Administration

  1. 01
    Reconstitution

    Vyleesi: pre-filled auto-injector. Research vial: 2 mL bacteriostatic water per 10 mg → 5 mg/mL.

  2. 02
    Injection site

    SQ — abdomen or thigh.

  3. 03
    Timing

    ≥45 min before sexual activity for peak effect. Effect persists ~6–8 h.

  4. 04
    Storage

    Vyleesi: room temp ≤30 °C. Research vial: refrigerate after reconstitution.

  5. 05
    Needle

    Auto-injector (Vyleesi) or 29–31G, 4–8 mm insulin syringe.

Appendix

Sources

32%

of 41 rendered claims carry a resolvable citation.

  1. [clayton-2015]
    Clayton 2015Bremelanotide for female sexual dysfunctions in premenopausal women
    J Sex Med, 2015
  2. [fda-vyleesi-label-2019]
    VYLEESI (bremelanotide injecti 2019VYLEESI (bremelanotide injection) prescribing information
    fda-label, 2019
  3. [simerly-2023]
    Simerly 2023Bremelanotide (PT-141): clinical pharmacology + safety review
    Sex Med Rev, 2023
Plate composed 2026-04-25 · maturity reviewed · schema v1 · Contributors: peptidesdb-core · 28 fields uncited — open contributions