PT-141 (Bremelanotide)
Melanocortin receptor agonist investigated for libido and sexual function in both sexes.

Research overview
PT-141, also known by its non-proprietary name bremelanotide, is a synthetic peptide analogue of the endogenous hormone α-Melanocyte-Stimulating Hormone (α-MSH). It was originally developed from Melanotan II as a research compound and has since been approved for a specific therapeutic use.
Its mechanism of action is centered on the central nervous system, where it functions as a non-selective agonist of the melanocortin receptors. Specifically, it is understood to activate the Melanocortin 4 Receptor (MC4R) and Melanocortin 3 Receptor (MC3R) in the brain. Unlike its parent compound, PT-141 has minimal activity at the Melanocortin 1 Receptor (MC1R) and therefore does not produce the skin tanning effect associated with Melanotan I and II. By activating these specific neural pathways, PT-141 modulates brain function related to sexual arousal and desire.
This selective action led to its development as a targeted therapeutic. PT-141, under the brand name Vyleesi, is an FDA-approved medication for the treatment of acquired, generalized hypoactive sexual desire disorder (HSDD) in premenopausal women, administered via subcutaneous injection on an as-needed basis.
Peer-Reviewed Research (PubMed)
Selected landmark / highly-cited studies indexed on PubMed.
- 1.Bremelanotide for the treatment of premenopausal women with acquired generalized hypoactive sexual desire disorder (RECONNECT trials)Kingsberg SA, et al. — Obstetrics & Gynecology, 2019
- 2.Double-blind, placebo controlled evaluation of the safety, pharmacokinetic properties and pharmacodynamic effects of intranasal PT-141, a melanocortin receptor agonist, in healthy males and patients with mild-to-moderate erectile dysfunctionDiamond LE, et al. — International Journal of Impotence Research, 2004
- 3.An effect on the subjective sexual response in premenopausal women with sexual arousal disorder by bremelanotide (PT-141), a melanocortin receptor agonistDiamond LE, et al. — Journal of Sexual Medicine, 2006
Studied benefits
- Activates MC4R pathways
- Studied for libido enhancement
- Centrally mediated mechanism
- Investigated in HSDD
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