Melanocortin receptor agonist · Also known as Bremelanotide, Vyleesi
An FDA-approved peptide (marketed as Vyleesi) for treating hypoactive sexual desire disorder (HSDD) in premenopausal women. Unlike PDE5 inhibitors that work on blood flow, PT-141 acts directly on the central nervous system to increase sexual desire.
PT-141 was originally developed as a sunless tanning agent derived from Melanotan II, but researchers discovered its potent effects on sexual arousal during clinical trials. In 2019 the FDA approved bremelanotide (Vyleesi) for HSDD in premenopausal women, making it the first injectable treatment for this condition. It works through a fundamentally different mechanism than drugs like sildenafil. rather than enhancing blood flow, it activates melanocortin receptors in the brain to modulate desire and arousal pathways.
PT-141 is a nonselective melanocortin receptor (MCR) agonist, with highest potency at MC1R and MC4R. The MC4R receptors in the hypothalamus are involved in regulating sexual behavior and arousal. By activating these central nervous system pathways, PT-141 increases sexual desire and arousal independent of peripheral blood flow mechanisms.
The exact mechanism by which PT-141 improves HSDD is not fully characterized, but activation of MC4R in the brain is thought to modulate dopaminergic and oxytocinergic pathways involved in sexual motivation. Because it works centrally rather than peripherally, it is effective for desire-related dysfunction in both men and women, though it is only FDA-approved for women.
1.75 mg as needed
Single dose, at least 45 min before activity1.75 mg as needed
OngoingMost side effects tend to improve as your body adjusts.