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Product Usage: This product is intended solely for use as a research chemical in vitro and laboratory experimentation by licensed, qualified professionals. It is not approved for human or animal consumption. Misuse, misbranding, or mislabeling as a drug, food, or cosmetic is strictly prohibited. All information provided is for educational purposes only.
PT-141
Product information
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Product description
PT-141, scientifically known as bremelanotide, is a synthetic peptide and melanocortin receptor agonist under investigation for its potential to address sexual dysfunction. It uniquely influences sexual arousal through central nervous system pathways rather than focusing on vascular mechanisms, distinguishing it from other treatments such as PDE5 inhibitors. PT-141 has gained approval for the management of generalized hypoactive sexual desire disorder (HSDD) in premenopausal women, demonstrating its clinical relevance.
Product Usage: This product is intended solely for use as a research chemical in vitro and laboratory experimentation by licensed, qualified professionals. It is not approved for human or animal consumption. Misuse, misbranding, or mislabeling as a drug, food, or cosmetic is strictly prohibited. All information provided is for educational purposes only.
- Characteristics
- How does PT-141 work?
- Research
- Side Effects
- Summary
- Certificate of Analysis (COA)
- References
Table of Contents
- Characteristics
- How does PT-141 work?
- Research
- Side Effects
- Summary
- Certificate of Analysis (COA)
- References
Characteristics
| NAME | ROLE |
|---|---|
Molecular Formula | C50H68N14O10 |
CAS Number | 189691-06-3 |
Molar Mass | 1025.2 g/mol |
Amino Acid Sequence | Ac-Nle-c[Asp-His-D-Phe-Arg-Trp-Lys]-OH |
Synonyms | Bremelanotide, PT-141, PT141, PT 141 |
Solubility | Water-soluble |
Organoleptic Profile | White to off-white powder |
Composition | Lyophilized powder |
How does PT-141 work?
PT-141 primarily acts as a melanocortin receptor agonist, with highest affinity for the melanocortin 4 receptor (MC4R) and melanocortin 1 receptor (MC1R). Research suggests the following mechanisms:
1. Central Nervous System: PT-141 activates MC4R in specific brain regions, particularly the hypothalamus and brainstem areas involved in sexual response. This activation is thought to influence neural pathways related to sexual desire and arousal.
2. Neurotransmitter Modulation: Studies indicate that PT-141 may increase dopamine release in the medial preoptic area, a region crucial for sexual motivation.
3. Peripheral Effects: PT-141's interaction with MC1R on melanocytes has been studied for potential effects on skin pigmentation.
Research
1. HSDD in Premenopausal Women:
Multiple Phase III clinical trials have evaluated PT-141's efficacy for HSDD.
Studies typically measured changes in sexual desire and related distress using validated scales like the Female Sexual Function Index (FSFI) and Female Sexual Distress Scale-Desire/Arousal/Orgasm (FSDS-DAO).
Research has examined various dosing regimens and administration methods.
2. Other Areas of Investigation:
Male Sexual Function: Some studies have explored potential effects on erectile function, though this is not an FDA-approved use.
Dermatology: Limited research has investigated PT-141's influence on melanogenesis and potential applications in pigmentation disorders.
Cardiovascular Effects: Studies have examined PT-141's impact on blood pressure and heart rate, primarily for safety monitoring.
Side Effects
Nausea
Flushing
Headache
Focal hyperpigmentation, which is generally reversible upon discontinuation of the drug
Summary
PT-141 (Bremelanotide) is a synthetic peptide that has been the subject of extensive clinical research, particularly in the field of female sexual health. It is approved use for HSDD in premenopausal women represents a significant development in this therapeutic area. Ongoing studies continue to explore its mechanisms of action, potential applications, and long-term safety profile.
References
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