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Peptidogen
“Laboratory Research Compounds”

PT-141

PT-141 (Bremelanotide) is a synthetic peptide analog of α-melanocyte–stimulating hormone (α-MSH), evaluated in controlled in vitro research for its agonist activity at melanocortin receptors, particularly MC3R and MC4R. Studies often investigate its influence on central neurochemical pathways, including those associated with sexual behavior, hormonal regulation, and peptide–receptor binding dynamics within the central nervous system. Experimental models may also assess its role in modulating neuronal signaling and neuroendocrine function. This compound is supplied exclusively for qualified laboratory research purposes and is not approved for human or veterinary administration, diagnostic use, or therapeutic application.

For laboratory research use only. Not for human or veterinary use. Not intended for diagnostic, therapeutic, or clinical applications.

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PT-141

Form: Scientific-grade, Lyophilized Powder

Purity: ≥99%

CAS Number: 189691-06-3

PT-141 is a research-use-only peptide investigated for its binding activity to melanocortin receptors, particularly MC4R. It is commonly explored in studies related to neurochemical signaling and peptide-mediated modulation of physiological responses.

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Chemical Structure & Identifiers

PubChem CID: 9941379 Structure: Laboratory Chemical Safety Summary (LCSS) Datasheet Molecular Formula: C50H68N14O10 Synonyms: Bremelanotide, PT-141, Bremelanotida, PT-141 Free Base, 189691-06-3, 6Y24O4F92S Molecular Weight: 1025.2 g/mol Computed by PubChem: (PubChem release 2025.04.14) Date Created: 2006-10-25 Last Modified: 2025-07-28

PT-141 (Bremelanotide) is provided for non-clinical research applications involving melanocortin receptor studies, neurochemical pathway analysis, and peptide-receptor binding. Not for diagnostic, therapeutic, or in vivo use.

 Molecular Structure

Mechanism of Action

PT-141 (Bremelanotide) is a synthetic melanocortin receptor agonist. Its primary mechanism of action involves selectively activating melanocortin receptors in the central nervous system, particularly the MC3R and MC4R subtypes. Unlike some other treatments for sexual dysfunction that target vascular mechanisms, PT-141 acts directly on neural pathways in the brain to influence sexual desire and arousal.

  • MC3R and MC4R Activation: These receptors are found in various brain regions, including the hypothalamus, which plays a crucial role in regulating appetite, energy expenditure, and sexual behavior. Activation of these specific receptors is believed to mediate the peptide's effects on sexual function.
  • Central Nervous System Pathway: By signaling through these brain receptors, PT-141 stimulates neural pathways that are distinct from those involved in physiological arousal (like blood flow) and instead directly influence central aspects of sexual response, such as desire and subjective arousal.
  • Modulation of Dopamine and Norepinephrine: While not fully elucidated, research suggests that the activation of MC3R and MC4R may lead to downstream effects on neurotransmitter systems, such as dopamine and norepinephrine, which are known to be involved in reward, motivation, and sexual behavior.

This central mechanism differentiates PT-141 from peripheral-acting drugs, making it a unique compound in research for certain types of sexual dysfunction.

Clinical Development & Research Focus

PT-141 (Bremelanotide) has undergone significant **clinical development**, particularly for the treatment of Hypoactive Sexual Desire Disorder (HSDD) in premenopausal women. It has been a subject of rigorous research due to its novel central mechanism of action, distinct from existing treatments. Key areas of research and clinical focus include:

  • Hypoactive Sexual Desire Disorder (HSDD): The primary focus of its clinical trials has been to evaluate its efficacy and safety in increasing sexual desire and reducing associated distress in women diagnosed with HSDD.
  • Erectile Dysfunction (ED) in Men: Earlier research and some clinical trials also investigated its potential for treating ED in men, particularly those who did not respond to traditional phosphodiesterase-5 (PDE5) inhibitors (e.g., sildenafil) due to its central mechanism.
  • Pharmacokinetics and Pharmacodynamics: Extensive studies have characterized its absorption, distribution, metabolism, and excretion, as well as its dose-response relationships and the duration of its effects.
  • Safety Profile and Side Effects: Clinical trials have meticulously documented common and rare side effects, including nausea, flushing, headache, and transient blood pressure increases, and have evaluated its overall safety profile for potential therapeutic use.

It's important to note that while Bremelanotide (PT-141) did receive FDA approval for HSDD under a specific brand name (Vyleesi®) via an injectable route, the research chemical PT-141 sold for laboratory use is not the approved pharmaceutical product and is strictly for research purposes, not for human consumption or therapeutic use.

Guidelines for Experimental Use

PT-141 is strictly intended for **laboratory research purposes only**. It should be handled by qualified personnel in a controlled environment, adhering to all applicable safety protocols and guidelines for research chemicals. This product is **not approved for human consumption, therapeutic use, or veterinary application**. It is solely for scientific investigation and analysis in a research setting. Proper laboratory safety equipment and procedures must be employed during its handling and experimental application.

Key Scientific References

Further information on PT-141 and related research can be found in the following scientific literature:

*(Note: Direct PubMed references for PT-141 are provided, including key clinical trials and reviews on its mechanism and applications in sexual dysfunction.)*

Storage and Handling Recommendations

For optimal stability and preservation of PT-141, observe the following recommendations:

  • Storage: Store lyophilized powder at -20°C to -80°C (long-term) or 2°C to 8°C (short-term, for up to 2-4 weeks), away from light and moisture.
  • Reconstitution: Reconstitute with sterile, deionized water or a suitable solvent as per specific experimental protocols. Avoid repeated freeze-thaw cycles.
  • Handling: Handle under aseptic conditions to prevent contamination. Use appropriate personal protective equipment (PPE), including gloves and eye protection.
  • Stability: Once reconstituted, solutions should be stored at 2°C to 8°C and used within a short period, typically 24-72 hours, depending on the solvent and concentration. Long-term storage of reconstituted solutions is not recommended.
  • Disposal: Dispose of PT-141 and any waste materials in accordance with local and institutional hazardous waste regulations.

Strict adherence to these guidelines will help maintain the integrity and purity of the compound for research applications.

Important Compliance Statement

This product, PT-141, is sold exclusively for **research and development purposes**. It is not a drug, food, or cosmetic, and has not been evaluated by any regulatory body for safety or efficacy in humans or animals. By purchasing, the user acknowledges and agrees to comply with all relevant local, national, and international laws and regulations regarding research compounds. Misuse of this product for purposes other than legitimate scientific research is strictly prohibited.

Analytical Validation & Documentation (COA, HPLC, MS)

Each production lot is subjected to rigorous analytical validation to confirm quality, purity, and molecular identity under research-grade standards. Full supporting documentation is available upon request.

  • COA (Certificate of Analysis): Includes batch number, purity percentage, traceability of each constituent ingredient, storage instructions, and full QC test results.
  • HPLC (High-Performance Liquid Chromatography): Provides chromatographic confirmation of purity and compound homogeneity.
  • MS (Mass Spectrometry): Confirms molecular weight and verifies structural integrity of the compound.
  • Traceability: Documents are traceable to their respective manufacturing lot and are intended to support reproducibility and transparency in scientific investigation.
  • COA Page 1 COA Page 2 COA Page 3

    Displayed above: Sample Certificate of Analysis – AOD-9604 (3-page image preview)

Storage & Shipping

All of our products are manufactured using the Lyophilization (Freeze Drying) process, which ensures stability during transit and long-term storage. Below are the official recommendations:

  • Stability During Shipping: Products are 100% stable for shipping for up to 3–4 months at ambient temperature.
  • After Reconstitution: Once reconstituted with bacteriostatic water, the peptide must be stored in a refrigerator and will remain stable for up to 30 days.
  • Room Temperature Storage: Lyophilized powder can be safely stored at room temperature until reconstitution, provided it remains sealed and protected from light.
  • Refrigerated Storage (Short Term): Store under 4°C (39°F) if not used immediately. Suitable for storage up to several weeks or months.
  • Frozen Storage (Long Term): For extended stability (months to years), store in a freezer at -80°C (-112°F).

Note: Avoid repeated freeze-thaw cycles. Always aliquot after reconstitution when necessary. Follow institutional safety protocols for handling all research compounds.

For advanced storage tips and reconstitution guidance, contact us or refer to our extended documentation.

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