Non-selective MCR agonist: activates MC1R (melanocortin-1, melanogenesis → tanning), MC3R + MC4R (satiety, energy expenditure), and MC5R (sebum / immune). The MC4R-mediated effects drive appetite suppression and the sexual-response effects that led to the related PT-141 (bremelanotide) development. Unregulated product contamination is common; associated with spontaneous-priapism case reports.
Dosing Guidelines
SC: Typical 0.5 mg (Range: 0.25–1 mg)
Target Organ Systems
endocrine
digestive
integumentary
immune-hematologic
Interactions
PT-141 (synergistic): Bremelanotide is the MC4R-preferring metabolite of MT-II. Do not stack.