Sexual Dysfunction. PT-141 (bremelanotide) is a synthetic peptide analog of α-MSH that acts on the melanocortin receptor system. Unlike PDE5...
PT-141 (bremelanotide) is a synthetic peptide analog of α-MSH that acts on the melanocortin receptor system. Unlike PDE5 inhibitors (Viagra, Cialis) which work on the vascular system, PT-141 works through the central nervous system to increase sexual desire. FDA-approved in 2019 as Vyleesi for hypoactive sexual desire disorder (HSDD) in premenopausal women.
PT-141 activates melanocortin-4 receptors (MC4R) in the hypothalamus, targeting desire and arousal at the neurological level rather than facilitating blood flow. Originally derived from Melanotan II, it was developed to isolate pro-sexual effects without tanning side effects.
Important: The evidence base for PT-141 varies by application. Many findings are from preclinical (animal or in vitro) studies. Large-scale human clinical trials may not be completed. Always evaluate the quality of evidence before drawing conclusions.
Nausea is the most common effect (~40% of trial participants). Other effects include flushing, headache, injection site reactions, and transient BP increases. FDA label warns of hyperpigmentation risk with repeated use. Limited to once per 24 hours, max 8 doses/month.
PT-141 (bremelanotide) is FDA-approved as Vyleesi for HSDD in premenopausal women. Off-label use requires a prescription. Available from compounding pharmacies and research suppliers.
These verified suppliers carry PT-141 with third-party COAs and US-based shipping.