By entering this website, you confirm that you are at least 21 years of age andunderstand: that all products are sold strictly for research use only, for in vitrolaboratory use.
These products are not approved by the FDA for human or animal consumption.
administration, or any form of bodily introduction, as prohibited by law.
Sort by
Display
per page
From $36.00
Melanotan-1 -10mg
BBT-US-30-699788
Melanotan-1, also known as afamelanotide, is a synthetic peptide analog of alpha-melanocyte-stimulating hormone (α-MSH). It interacts with melanocortin receptors, particularly MC1R, to increase eumelanin production in the skin, which enhances natural photoprotection.
It has been extensively studied in relation to photosensitivity disorders such as erythropoietic protoporphyria (EPP), and is distinct from Melanotan-II due to its higher receptor selectivity and reduced off-target activity.
From $36.00
From $39.00
Melanotan-2 -10mg
PPT- US-881234
Melanotan-2 (MT-II) is a synthetic peptide analog of alpha-melanocyte-stimulating hormone (α-MSH). It activates melanocortin receptors involved in pigmentation, sexual behavior, appetite regulation, and energy balance. Originally developed to study enhanced melanin production and photoprotection, MT-II is now widely researched for its multifaceted neuroendocrine and metabolic effects.
From $39.00
From $45.00
PT-141 (Bremelanotide) -10mg
BBT-US-30-699799
PT-141, also known as Bremelanotide, is a synthetic peptide derived from the melanocortin family. Unlike PDE-5 inhibitors (e.g., sildenafil) that act on vascular pathways, PT-141 works centrally by activating melanocortin receptors (MC3R/MC4R) in the brain. This mechanism enhances sexual desire and arousal through neural circuits linked to motivation and reward. It has been studied for both erectile dysfunction (ED) in men and hypoactive sexual desire disorder (HSDD) in women.
From $45.00
From $33.00
PT-141 (Bremelanotide) – 5mg
BBT-US-35-995386
PT-141, also known as Bremelanotide, is a synthetic peptide derived from the melanocortin family. Unlike PDE-5 inhibitors (e.g., sildenafil) that act on vascular pathways, PT-141 works centrally by activating melanocortin receptors (MC3R/MC4R) in the brain. This mechanism enhances sexual desire and arousal through neural circuits linked to motivation and reward. It has been studied for both erectile dysfunction (ED) in men and hypoactive sexual desire disorder (HSDD) in women.
From $33.00