Laboratory research materials for in vitro use only.

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PT-141

For laboratory research use only (in vitro). Not for human or animal use.

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Certificate of Analysis available upon request. Contact us for lot-specific documentation.

Product Specifications

Amino Acid Sequence Ac-Nle-c[Asp-His-D-Phe-Arg-Trp-Lys]-OH
Molecular Weight 1025.18 Da
Molecular Formula C50H68N14O10
CAS Number 189691-06-3
Purity ≥98% (HPLC)
Format Lyophilized Powder
Net Quantity 10mg
Vials Per Kit 10
Storage Store at -20C. Reconstituted: 2-8C
Research Status Approved

For laboratory research use only (in vitro). Not for human or animal use.

Description

Chemical Identity

PT-141 (Bremelanotide) is a synthetic cyclic heptapeptide with the molecular formula C50H68N14O10 and a molecular weight of 1025.18 Da (CAS number 189691-06-3). The amino acid sequence is Ac-Nle-c[Asp-His-D-Phe-Arg-Trp-Lys]-OH, structurally derived from Melanotan-2 but with a free carboxylic acid C-terminus instead of an amide. PT-141 was developed as a selective melanocortin receptor agonist for sexual dysfunction research.

PT-141 has received FDA approval under the brand name Vyleesi for hypoactive sexual desire disorder (HSDD) in premenopausal women, making it the first melanocortin receptor-targeted compound approved for a sexual dysfunction indication.

Property Value
Molecular Formula C50H68N14O10
Molecular Weight 1025.18 Da
CAS Number 189691-06-3
Sequence Ac-Nle-c[Asp-His-D-Phe-Arg-Trp-Lys]-OH
Research Status FDA-approved (Vyleesi)

Research Overview

PT-141 has been investigated through the complete clinical development pathway, culminating in FDA approval. The primary mechanism involves selective agonism of melanocortin-4 receptors (MC4R) in the central nervous system, particularly in hypothalamic regions involved in sexual arousal and desire. Unlike phosphodiesterase inhibitors that act peripherally on vascular smooth muscle, PT-141 acts centrally through neuronal pathways to modulate sexual function.

The development of PT-141 from Melanotan-2 illustrates rational drug design, where the melanogenesis-focused parent compound was modified to reduce MC1R-mediated pigmentation effects while preserving MC4R-mediated effects on sexual function.

Key areas of published research include:

  • Hypoactive Sexual Desire Disorder: Pivotal Phase 3 trials (RECONNECT studies) demonstrated that PT-141 significantly improved sexual desire, arousal, and associated distress scores compared to placebo in premenopausal women with HSDD, leading to FDA approval in 2019.
  • Male Erectile Function: Earlier clinical studies evaluated PT-141 for erectile dysfunction, demonstrating efficacy through a central mechanism distinct from PDE5 inhibitors. The compound showed activity in patients unresponsive to conventional treatments.
  • Melanocortin Receptor Pharmacology: PT-141 has been instrumental in characterizing the role of MC4R in sexual function, establishing this receptor as a validated therapeutic target for sexual dysfunction.

PT-141 is FDA-approved as Vyleesi for HSDD in premenopausal women. Research-grade material is available for preclinical studies.

Specifications

All PT-141 supplied by Prescott Bio Canada is manufactured to research-grade standards.

Specification Detail
Purity >98% (HPLC)
Form Lyophilized powder
Appearance White to off-white powder
Storage (lyophilized) -20°C, protected from light
Storage (reconstituted) 2-8°C, use within 30 days
Solubility Soluble in bacteriostatic water, sterile water, or normal saline

Each vial is accompanied by a Certificate of Analysis (COA) documenting purity, identity, and endotoxin testing.

Research Applications

PT-141 is supplied exclusively for in vitro and in vivo laboratory research. Published experimental applications include:

  • Melanocortin-4 receptor signaling and sexual function research
  • Central nervous system pathways of sexual arousal and desire
  • Comparative melanocortin receptor selectivity studies
  • Neuroendocrine regulation of reproductive behavior
  • Structure-activity relationship studies with melanocortin peptide analogs

Researchers should consult the primary literature and institutional review protocols before designing experiments with PT-141.

Storage and Handling

Lyophilized powder: Store at -20°C in the original sealed vial, protected from light and moisture. Under these conditions, PT-141 maintains stability for up to 24 months.

Reconstituted solution: Reconstitute with bacteriostatic water or sterile water. Store reconstituted PT-141 at 2-8°C and use within 30 days. Avoid repeated freeze-thaw cycles.

Handling precautions: This product is intended for research use only (RUO). Not for human or veterinary diagnostic or therapeutic use. Handle using standard laboratory safety practices including appropriate PPE.

Additional information

Size

10mg

Published Research

5 references

References are provided for informational purposes to support in vitro laboratory research. No claims are made regarding therapeutic applications.

Bremelanotide for the Treatment of Hypoactive Sexual Desire Disorder: Two Randomized Phase 3 Trials

Kingsberg SA, Clayton AH, Portman D, Williams LA, Krop J, Jordan R, Lucas J, Simon JA (2019). Obstetrics and Gynecology. PubMed 31599840

Safety Profile of Bremelanotide Across the Clinical Development Program

Clayton AH, Kingsberg SA, Portman D, Sadiq A, Krop J, Jordan R, Lucas J, Simon JA (2022). Journal of Women's Health. PubMed 35147466

The neurobiology of bremelanotide for the treatment of hypoactive sexual desire disorder in premenopausal women

Pfaus JG, Sadiq A, Spana C, Clayton AH (2022). CNS Spectrums. PubMed 33455598

Melanocortins in the treatment of male and female sexual dysfunction

Shadiack AM, Sharma SD, Earle DC, Spana C, Hallam TJ (2007). Current Topics in Medicinal Chemistry. PubMed 17584134

Bremelanotide: New Drug Approved for Treating Hypoactive Sexual Desire Disorder

Mayer D, Lynch SE (2020). Annals of Pharmacotherapy. PubMed 31893927

For laboratory research use only (in vitro). Not for human or animal use.

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