Description
About PT-141
PT-141 is a cyclic heptapeptide melanocortin-receptor agonist derived from the α-MSH scaffold, supplied as a lyophilised research compound. The lactam bridge constrains the peptide backbone into a defined conformation, which is why this melanocortin agonist is widely used as a reference ligand for receptor-subtype selectivity work in vitro.
Key features of PT-141
- Cyclic melanocortin receptor agonist (7-amino-acid)
- Sequence: Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH (7 amino acids)
- Lyophilised solid — stable, easy to store, straightforward to reconstitute
- Unit size: 10 mg / vial
- Every batch released only after identity, purity, and appearance QC
- Certificate of Analysis (CoA) and batch documentation available on request
PT-141 technical specifications
| Product name | PT-141 |
| Synonyms | Bremelanotide; PT-141 acetate; melanocortin receptor agonist |
| Amino-acid sequence | Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH |
| Class | Cyclic melanocortin receptor agonist (7-amino-acid) |
| Molecular formula | C₅₀H₆₈N₁₄O₁₀ (free base) |
| Molecular weight | ~1,025.2 g/mol |
| CAS number | 189691-06-3 |
| Purity | ≥99% (HPLC) |
| Physical form | Lyophilised powder |
| Appearance | White to off-white solid |
| Unit size | 10 mg / vial |
| Note | Lactam-bridged cyclic structure derived from the α-MSH scaffold |
Reconstituting and storing PT-141
- Before reconstitution: Store lyophilised vials at 2–8 °C, protected from light and moisture.
- Equilibrate: Allow vial and diluent to reach room temperature before opening.
- Reconstitute: Add Bacteriostatic Water (10 ml recommended). Swirl gently — do not vortex.
- After reconstitution: Store at 2–8 °C. Prepare aliquots to minimise freeze–thaw cycles.
- Compatibility: Use only within protocols that comply with your institution’s SOPs and local regulations.
Looking for complementary materials? See Bacteriostatic Water 10ml — recommended diluent, KPV 10mg — minimal melanocortin fragment, Oxytocin 2mg.
PT-141 in research
Researchers examine PT-141 to characterise receptor engagement across the melanocortin subtypes, profile G-protein and cAMP second-messenger responses, and establish structure-activity relationships between constrained and linear α-MSH analogues in cell-based assays. Its conformational rigidity makes this melanocortin agonist a useful probe when distinguishing MC3R from MC4R responses.
Synthesis and quality assurance
Avanti Peptides manufactures PT-141 via controlled, validated solid-phase peptide synthesis (SPPS) to deliver high purity and lot-to-lot consistency. Each batch undergoes identity verification, HPLC purity analysis (≥99%), and appearance inspection before release.




