PT-141 (10mg)
Technical Specifications
| Purity (HPLC) | ≥99% (HPLC) |
| CAS Number | 189691-06-3 |
PT-141 (10mg)
| Purity (HPLC) | ≥99% (HPLC) |
| CAS Number | 189691-06-3 |
| Form | White lyophilized powder |
| Storage | -20°C |
| Sequence | Ac-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH |
| Molecular Weight | 1,025.21 g/mol |
| Salt Form | Acetate |
| Solubility | Soluble in water |
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Melanocortin receptor agonist for CNS research.
Mechanism: Agonist at MC3R/MC4R in hypothalamus, activates central arousal pathways.
Applications: Sexual function models, melanocortin studies, CNS pharmacology.
Note: FDA-approved as Vyleesi® for HSDD.
Strictly for Laboratory Research Use Only.
Not for human consumption, veterinary use, or diagnostic purposes.
A cyclic heptapeptide melanocortin receptor agonist (primarily MC4R) developed from the Melanotan II scaffold. Unlike phosphodiesterase inhibitors, PT-141 acts centrally through hypothalamic melanocortin pathways, representing a mechanistically distinct approach to sexual function research.
A cyclic heptapeptide melanocortin receptor agonist (primarily MC4R) developed from the Melanotan II scaffold. Unlike phosphodiesterase inhibitors, PT-141 acts centrally through hypothalamic melanocortin pathways, representing a mechanistically distinct approach to sexual function research.
Origin: Derived from Melanotan II; developed by Palatin Technologies
Commonly studied routes: Subcutaneous. Reconstitute with bacteriostatic water. Consult published literature for dose ranges; use our Peptide Calculator for volumetric preparation.
-20°C lyophilized, 2-8°C reconstituted
PT-141 (10mg) is supplied for laboratory research use only (RUO). Not for human or veterinary use, diagnostics, or therapeutics.
Synthesized for strict analytical consistency. Verified via HPLC/MS.View Quality Standards →