Precision Research ChemicalsThird-Party TestedBatch-Specific CoASame-Day Shipping14 Compounds99%+ Purity
Precision Research ChemicalsThird-Party TestedBatch-Specific CoASame-Day Shipping14 Compounds99%+ Purity
KERN
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PT-141 (Bremelanotide) (10mg)

PT-141

Melanocortin receptor agonist derived from Melanotan II. FDA-approved analog Vyleesi indicated for HSDD. Research analog for in vitro study.

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$189$194.85USD

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Research Use Only. This product is intended for laboratory research purposes only. Not for human or veterinary use. Not for sale to minors.

Certificate of Analysis

Latest

Independent third-party analytical certificates for PT-141. A batch-specific CoA is provided with every purchase.

01At a Glance01 / 08

PT-141 — Key Data

A snapshot of published research on PT-141. Each figure links to the literature summarized below.

Women Studied (Phase 3)
0RECONNECT trials, double-blind, placebo-controlled
Satisfying Sexual Events
0vs 9.8% placebo (p < .001)
Sildenafil Non-Responders
0Response rate in male ED
Approved (Vyleesi)
0For premenopausal women with HSDD
Onset
0Subcutaneous administration before activity
02Mechanism02 / 08

How PT-141 Works

PT-141 (Bremelanotide) is a melanocortin receptor agonist derived from Melanotan II, designed to concentrate binding at MC3R and MC4R. Unlike PDE5 inhibitors (sildenafil), it works centrally on the nervous system. The FDA-approved analog Vyleesi is indicated for HSDD in premenopausal women. In male ED, 33% of sildenafil non-responders responded to bremelanotide. Onset is approximately 45 minutes. For research use only.

Discovered ~2000100+ publicationsActive metabolite of Melanotan II; developed by Palatin Technologies

  1. 01

    MC4R Central Activation

    Primary
    • High affinity for MC4R (primary target for sexual function)
    • Central nervous system mechanism (not peripheral like PDE5i)
    • Nanomolar potency at melanocortin receptors
03Findings03 / 08

What the Studies Show

Peer-reviewed outcomes from published PT-141 research.

0

RECONNECT Phase 3 trials (n=1,267). vs 9.8% placebo (p < .001). FSFI desire domain improvement: +0.35 vs placebo.

Kingsberg et al., 2019

Additional Clinical Outcomes

  1. 0

    n=342 male ED patients. ~86% achieved erections within 1 hour. Mean intercourse frequency increased from 1.2 to 2.2/week.

    Rosen et al., 2003

Mechanism of Action Comparison

Central (MC4R in hypothalamus)
PT-141 (Bremelanotide)
Peripheral (PDE5 in vasculature)
Sildenafil (Viagra)
33% response rate
PT-141 in Sildenafil Non-Responders

Central mechanism means PT-141 can work when peripheral approaches fail

04Applications04 / 08

Research Applications

Reported areas of investigation across the PT-141 literature.

  1. 01
    FEMALE SEXUAL HEALTH

    HSDD Phase 3 Results (1,267 Women)

    25% increase in satisfying sexual events vs 9.8% placebo in the RECONNECT Phase 3 trials. FDA-approved as Vyleesi.

    Satisfying events increase
    +25%
    Placebo increase
    +9.8%
    Significance
    p < .001

    Study finding. FSFI desire domain improvement: +0.35 vs placebo. Double-blind, placebo-controlled.

    Kingsberg et al., 2019
  2. 02
    MALE SEXUAL HEALTH

    Response in PDE5 Inhibitor Non-Responders

    33% of sildenafil non-responders achieved erections with bremelanotide. ~86% achieved erections within 1 hour.

    Non-responder response rate
    33%
    Erection within 1 hour
    ~86%
    Intercourse frequency
    1.2 to 2.2/week

    Study finding. n=342 male ED patients. Central mechanism enables response where peripheral approaches fail.

    Rosen et al., 2003
05Safety05 / 08

Reported Observations

  • 40%Nausea: 40.0% vs 1.3% placebo (median duration 2.4 hours)
  • Blood pressure: systolic +3 mmHg, diastolic +2 mmHg (returned to baseline by 8-10h)
  • Flushing (20.6%), headache (12.0%)
  • Max: 1 dose per 24 hours, max 12 doses per 4-week period

This summary reflects observations from published peer-reviewed research. It is not a comprehensive safety assessment. Researchers should review primary literature before designing protocols. For Research Use Only.

06Compound06 / 08

Compound Profile

Molecular Profile

What Is PT-141?

TypeSynthetic Cyclic Heptapeptide (Melanocortin Agonist)
CAS Number189691-06-3
Molecular Weight1,025.16 g/mol
Amino Acids7 (cyclic)
SequenceAc-Nle-cyclo[Asp-His-D-Phe-Arg-Trp-Lys]-OH
FormulaC50H68N14O10
View on PubChem
Storage & Handling

Stability Information

  • Protect from light
  • Avoid repeated freeze-thaw cycles
  • Store in original sealed container

Lyophilized (powder)

up to 2 years

-20°C

Reconstituted

up to 30 days

2-8°C

Working solution

Use within 24 hours

Room temp
07Questions07 / 08

PT-141 (Bremelanotide) is a melanocortin receptor agonist derived from Melanotan II. It selectively targets MC3R and MC4R receptors in the central nervous system, which are involved in sexual arousal and desire. An FDA-approved version (Vyleesi) was approved in 2019 for the treatment of hypoactive sexual desire disorder (HSDD) in premenopausal women. The research-grade form is used for in vitro and preclinical studies.

The pharmaceutical version (Bremelanotide, brand name Vyleesi) is FDA-approved specifically for HSDD in premenopausal women. It is not approved for use in men or for general sexual function enhancement. Research-grade PT-141 is a separate product sold exclusively for laboratory and in vitro research purposes. For Research Use Only.

PDE5 inhibitors (such as sildenafil and tadalafil) work by increasing blood flow through vasodilation. They address the mechanical/vascular component of sexual function. PT-141 works in the central nervous system by activating melanocortin receptors involved in sexual desire and arousal. It operates upstream at the level of desire rather than downstream at the level of blood flow. These are fundamentally different mechanisms.

In the clinical trials that led to FDA approval, nausea was the most common side effect, occurring in approximately 40% of subjects. Other reported effects include headache, flushing, transient blood pressure elevation, and mild hyperpigmentation with repeated administration. The 12-month safety extension study includes a warning about blood pressure effects and limits use to no more than 8 administrations per month.

PT-141 selectively targets MC3R and MC4R (sexual function pathways) with minimal MC1R activation (pigmentation). Melanotan II activates all melanocortin receptor subtypes broadly, producing both tanning and sexual function effects along with appetite suppression. PT-141 was developed specifically to isolate the sexual function response.

Store lyophilized PT-141 at -20C. Reconstitute with bacteriostatic water and refrigerate at 2-8C. Use reconstituted vials within 30 days.

Every batch undergoes third-party HPLC and mass spectrometry testing. HPLC confirms purity (99%+ standard). Mass spectrometry confirms molecular identity. A batch-specific Certificate of Analysis is provided with every purchase and available for download directly on this page.

All Kern products ship same-day (orders placed before 1pm EST). Lyophilized peptides are shipped at ambient temperature and are stable during transit. Upon receipt, store at -20C for long-term stability or 2-8C for near-term use. If the product arrives damaged, contact us within 7 days with photos for a free replacement.

Price differences usually reflect differences in purity, testing standards, and manufacturing quality. Low-cost vendors may skip mass spectrometry verification (which confirms you actually have the right molecule), use lower-grade raw materials, or skip sterility and endotoxin testing. Kern tests every batch with both HPLC and mass spec, and our CoAs are available before you buy.

08References08 / 08

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The statements made within this website have not been evaluated by the US Food and Drug Administration. The products we offer are not intended to diagnose, treat, cure, or prevent any disease. The peptides sold on this website are intended for research use only. The buyer is responsible for adhering to all local laws and regulations. Kern is not a pharmacy and does not provide medical advice or prescriptions. They are not for human consumption, are not FDA approved, and are not supplements or pharmaceutical drugs. The information provided on this website is for informational purposes and not a substitute for professional medical advice, diagnosis, or treatment. If you have questions or concerns about your health, please talk to your doctor. This site is an advertisement for education, research peptides, and not any specific medication. By purchasing from Kern, you confirm that you are a qualified researcher purchasing these compounds for legitimate in vitro or laboratory research purposes only. You must be 21 years of age or older to purchase.