peptides_direct
BitcoinTether USDTEthereumSolana+ more5% Crypto DiscountSEPA bank transferSEPA
PT-141
Back soon
Growthhormonal

PT-141

Cyclic heptapeptide (bremelanotide) that acts as a melanocortin receptor agonist at MC3R and MC4R in the central nervous system. The active metabolite of Melanotan-II, studied for sexual-function endpoints via a central rather than vascular pathway.

€29.99

€39.99

Save 25%
This product will be back in stock soon.

Get notified when this product is back in stock.

Payment Methods

|
SEPA
|
Crypto
No customs within the EUFast tracked DHL shippingTrustpilotIndependent lab testing on selected batches

Melanocortin receptor agonist

Acts on melanocortin receptors, with research attention focused on MC3R and MC4R in the central nervous system.

Cyclic heptapeptide

A ring-shaped peptide of seven amino acids, chemically the active metabolite of the melanocortin analogue Melanotan-II.

Central, not vascular

Studied for signalling in the hypothalamus, a mechanism described in the literature as central rather than acting on blood vessels.

Clinically studied compound

Unusually for this category, bremelanotide has been through randomised, placebo-controlled clinical trials.

No EU marketing authorisation

Authorised in the United States under a brand name, but not approved as a medicinal product in the EU. Supplied strictly as a research material.

Lyophilized powder

Supplied freeze-dried, the standard form used across the published research.

Research areas

Melanocortin signallingMC3R & MC4RNeuropeptidesCentral nervous systemSexual-function research

What is PT-141

PT-141, also called bremelanotide, is a synthetic cyclic peptide built from seven amino acids arranged in a ring. Chemically it is the active metabolite of Melanotan-II: when Melanotan-II is metabolised, bremelanotide is the fragment that remains active at melanocortin receptors.

The peptide came out of melanocortin research at the University of Arizona and was developed further by Palatin Technologies. Unlike most compounds in this category, bremelanotide went through the full clinical development path, including randomised, placebo-controlled Phase 3 trials, and holds a marketing authorisation in the United States under the brand name Vyleesi for a specific indication in premenopausal women.

There is no EU marketing authorisation for bremelanotide. We supply it as a lyophilized (freeze-dried) powder for laboratory research only, not as a medicine.

How it works

Bremelanotide is a melanocortin receptor agonist. The melanocortin system is a family of five receptors (MC1R to MC5R) sitting at the centre of several regulatory circuits: pigmentation, inflammation, energy balance and sexual function. Bremelanotide is active at several of them, and the research attention sits on MC3R and MC4R.

The distinction the literature keeps returning to is where it acts. Research compounds targeting PDE5 work on vascular smooth muscle and change blood flow. Bremelanotide instead acts on melanocortin receptors in the brain, which is why it is described as a central mechanism rather than a vascular one. In animal models, activation of MC4R in hypothalamic circuits alters signalling associated with sexual behaviour independently of the vascular route.

Its relationship to Melanotan-II explains part of the receptor profile. Melanotan-II is a broad melanocortin agonist with strong MC1R activity, and MC1R is the receptor that drives pigmentation. Bremelanotide differs structurally at the C-terminus and shows comparatively less of that pigmentation-driving activity, which is why the two peptides are studied for different endpoints despite being closely related.

One caution that matters for interpreting the literature: bremelanotide, Melanotan-II and afamelanotide are three distinct chemical entities. Findings for one should not be transferred to the others.

Often studied alongside

Melanotan-II is the parent compound PT-141 derives from, and the two are routinely discussed together in melanocortin research.

For reconstitution, the standard solvent used in published protocols is bacteriostatic or sterile water.

Documentation

Material specification

Purity

≥99% (HPLC verified)

Test method

HPLC + mass spectrometry

Form

Lyophilized powder

Storage (sealed)

2 to 8 °C, light-protected

Storage (reconstituted)

2 to 8 °C, use within 4 weeks

CoA

Batch-specific, third-party (Janoshik)

Research use only

This material is sold strictly for in-vitro research and laboratory use. Not intended for human or animal consumption, medical, cosmetic, or household applications. Suitable only for professional laboratory environments.

Storage and stability

  • Dry, lyophilized vials keep for months refrigerated, or up to 24 months frozen at -20°C.
  • After reconstitution in bacteriostatic water, use within about 30 days at 2 to 8°C, and avoid repeated freeze-thaw.
See the full storage and stability timeline

Frequently Asked Questions