Catalog/Sexual Health/PT-141 (Bremelanotide)
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PT-141 (Bremelanotide)

Melanocortin receptor agonist

CAS Number

189691-06-3

Molecular Weight

1025.18 g/mol

Available Forms
Lyophilized Powder
Available Sizes
10mg20mg

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Research Areas
Sexual Function ResearchMelanocortin SignalingCNS PharmacologyFemale HSDD

Melanocortin receptor agonist for sexual health research. PT-141 is a synthetic peptide that activates melanocortin receptors in the central nervous system, with FDA approval for hypoactive sexual desire disorder in premenopausal women.

PT-141 (Bremelanotide) Research Compound

Research Use Only

This product is intended for laboratory research purposes only. It is not intended for human or veterinary use, food, cosmetic, household, or agricultural applications. Not for human consumption.

Overview

PT-141 (Bremelanotide) is a synthetic cyclic heptapeptide melanocortin receptor agonist. Originally derived from the tanning peptide Melanotan II, PT-141 was developed specifically for its effects on sexual function mediated through central nervous system melanocortin pathways. In 2019, it was FDA-approved as Vyleesi for the treatment of hypoactive sexual desire disorder (HSDD) in premenopausal women, making it the first peptide drug approved for this indication.

Molecular Characteristics

PropertyValue
Molecular FormulaC50H68N14O10
Molecular Weight1025.18 g/mol
CAS Number189691-06-3
SequenceAc-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH
StructureCyclic heptapeptide
Purity≥99% (HPLC)
Storage-20°C, protected from light

Mechanism of Action

PT-141 acts through melanocortin receptor activation in the CNS:

MC4R Activation

  • Primary target: Melanocortin-4 receptor (MC4R)
  • Secondary: MC3R and MC1R binding
  • Hypothalamic signaling pathway
  • Limbic system activation

Central Nervous System Effects

  • Not dependent on vascular mechanisms
  • Dopaminergic pathway interactions
  • Oxytocin system modulation
  • Emotional/motivational circuit activation

Distinct Mechanism

  • Works at CNS level (not peripheral)
  • Different from PDE5 inhibitors
  • Effects on desire, not mechanics
  • Both sexes responsive in research

Research Applications

Sexual Function Research

  • Desire vs. arousal pathways
  • Gender-comparative studies
  • Melanocortin pharmacology
  • CNS sexual response mapping

Melanocortin Receptor Studies

  • Receptor binding profiles
  • Signal transduction analysis
  • MC4R function research
  • Receptor subtype selectivity

CNS Pharmacology

  • Blood-brain barrier penetration
  • Central vs. peripheral effects
  • Neuroimaging studies
  • Behavioral pharmacology

Gender-Specific Research

  • Female HSDD models
  • Male erectile function
  • Comparative mechanism studies
  • Hormonal interaction research

Available Formats

SizeFormatCatalog Code
10mgLyophilizedPT-10
20mgLyophilizedPT-20

Handling & Storage

  • Store lyophilized peptide at -20°C
  • Protect from light and moisture
  • Reconstitute with bacteriostatic water
  • Reconstituted solution stable at 2-8°C for up to 3 weeks
  • Contains tryptophan (light-sensitive)
  • Avoid repeated freeze-thaw cycles

Quality Specifications

  • Purity: ≥99% by HPLC
  • Appearance: White lyophilized powder
  • Solubility: Soluble in water
  • Endotoxin: Less than 1 EU/mg
  • Certificate of Analysis provided

Regulatory Status

RegionStatus
USAFDA-approved (Vyleesi) for premenopausal women with HSDD
ResearchAvailable for research purposes
CompoundPrimary EffectReceptor Profile
PT-141Sexual functionMC4R > MC3R > MC1R
Melanotan IITanning + libidoMC1R > MC4R
Alpha-MSHPigmentationMC1R primary

References

  1. Kingsberg SA, et al. "Bremelanotide for the treatment of hypoactive sexual desire disorder." Obstet Gynecol. 2019.
  2. Clayton AH, et al. "Bremelanotide for female sexual dysfunctions in premenopausal women." Exp Opin Investig Drugs. 2018.
  3. Pfaus JG, et al. "A review of the role of melanocortins in sexual function." J Sex Med. 2007.

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