PT-141 (10mg)
Melanocortin Agonists

PT-141 (10mg)

Research PT-141 vial, dispatched from Australian stock. In Stock

$99.99AUD, GST inclusive · $10.00 per mg
CoA on request10mg per vialLyophilised powderSame business day dispatch*

Cyclic melanocortin agonist (MC3R/MC4R) derived from Melanotan II

PT-141 is the deamidated metabolite of Melanotan II, developed after MT-II's sexual-response effect was noticed in early trials. It acts centrally through MC3R and MC4R rather than on blood flow, which distinguishes it from PDE5 inhibitors. As bremelanotide it is registered in the United States for hypoactive sexual desire disorder in premenopausal women.

How it works

MC4R activation in the hypothalamus and limbic system modulates dopaminergic pathways involved in sexual arousal. The effect is independent of vascular mechanisms, which is why PT-141 has been studied in cases where vasodilators fail.

What the research reports

Phase 3 RECONNECT trials (Kingsberg et al., Obstet Gynecol 2019) reported increased sexual-desire scores versus placebo. Earlier trials in men with erectile dysfunction reported responses independent of nitric-oxide pathways.

Key research areas

  • Central arousal pathways — MC4R and dopamine interaction
  • Sexual-desire research — RECONNECT Phase 3 program
  • Non-vascular mechanisms — Comparison with PDE5 inhibitors
  • Melanocortin pharmacology — Relationship to MT-II

Also known as: Bremelanotide, Vyleesi (US brand), pt141, bremelanotide, Vyleesi (brand)

Certificate of analysis. Every batch carries a certificate from an independent laboratory. Request the certificate for your batch with your order number and we send it.

Specifications

Compound
PT-141
CAS number
189691-06-3
Category
Melanocortin Agonists
Vial size
10mg
Certificate of analysis
Available on request
Form
Lyophilised powder
Suggested reconstitution
2 mL bacteriostatic water
Storage (lyophilised)
−20 °C, protect from light and moisture
Storage (reconstituted)
2–8 °C, use within 8–12 weeks
SKU
PEP-035-10MG

Reconstitution calculator for this vial

Full calculator →
Concentration5 mg/mL5000 mcg/mL
Per syringe unit50 mcg0.01 mL per unit
Units for the amount10 units0.10 mL
Draws per vial20at 0.5 mg each

For in-vitro research and laboratory use only. Not for human or veterinary use. By purchasing you confirm you are a qualified researcher and will use this compound in accordance with all applicable laws.

Frequently asked questions

What is PT-141?

Cyclic melanocortin agonist (MC3R/MC4R) derived from Melanotan II. PT-141 is the deamidated metabolite of Melanotan II, developed after MT-II's sexual-response effect was noticed in early trials. It acts centrally through MC3R and MC4R rather than on blood flow, which distinguishes it from PDE5 inhibitors. As bremelanotide it is registered in the United States for hypoactive sexual desire disorder in premenopausal women.

What is PT-141 studied for?

Central arousal pathways: mC4R and dopamine interaction. Sexual-desire research: rECONNECT Phase 3 program. Non-vascular mechanisms: comparison with PDE5 inhibitors. Melanocortin pharmacology: relationship to MT-II. Phase 3 RECONNECT trials (Kingsberg et al., Obstet Gynecol 2019) reported increased sexual-desire scores versus placebo. Earlier trials in men with erectile dysfunction reported responses independent of nitric-oxide pathways.

PT-141 before and after: what do the studies show?

RECONNECT Phase 3 trials reported increased sexual-desire scores and reduced distress versus placebo in premenopausal women; earlier studies in men reported erectile responses independent of nitric oxide.

What side effects has PT-141 research reported?

Nausea was the most common event (around 40% in the Phase 3 trials), plus flushing, headache and transient blood-pressure increases; skin and gum darkening were reported with repeated use.

What is the PT-141 dosage?

Published PT-141 studies specify their own amounts and routes, and those vary by model and endpoint. Peptide Aus products are supplied for in-vitro laboratory research, so we do not provide dosing, cycle or usage guidance for people. For laboratory preparation, the reconstitution calculator converts vial size and water volume into concentration and syringe units.

PT-141 nasal spray or the vial?

Bremelanotide was trialled as a nasal spray before the registered product became an injection. Sprays sold online are unverified; Peptide Aus supplies the 10mg vial for research.

PT-141 vs Melanotan II: what is the difference?

PT-141 is the deamidated metabolite of MT-II, keeping the central sexual-response effect.

PT-141 vs sildenafil: what is the difference?

PDE5 inhibitors act on blood flow; PT-141 acts centrally on melanocortin receptors.

How do you reconstitute PT-141 (10mg)?

Add about 2 mL of bacteriostatic water slowly down the inside of the vial and swirl gently; do not shake. 10mg in 2 mL gives 5 mg/mL. Refrigerate at 2–8 °C after reconstitution and use within 8–12 weeks. The calculator has this vial preset.

How should PT-141 be stored?

Lyophilised: −20 °C, sealed, away from light and moisture. Reconstituted: 2–8 °C, used within 8–12 weeks, never frozen.

Is PT-141 legal in Australia?

Bremelanotide is registered in the United States but not by the TGA, so there is no approved PT-141 product in Australia. Peptide Aus supplies research-grade PT-141 for in-vitro laboratory use only.

Where can I buy PT-141 in Australia, and what does it cost?

Directly from Peptide Aus, from Australian stock: PT-141 (10mg) is $99.99 AUD including GST. Paid orders before 2pm AEST/AEDT dispatch the same business day, tracked.

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