PT-141 10mg

PT-141 10mg

$45.00

Melanocortin receptor agonist studied for sexual function and libido research. 10mg | For research and laboratory use only.

PT-141 (Bremelanotide) is a synthetic cyclic peptide analogue of alpha-melanocyte-stimulating hormone (α-MSH) that acts as a melanocortin receptor agonist. Unlike other compounds studied in sexual health research, PT-141 works through the central nervous system by targeting melanocortin receptors rather than the vascular system.

In laboratory research, PT-141 has been investigated for its potential effects on sexual arousal, libido, and related neurological pathways in both male and female experimental models. Its interaction with MC3R and MC4R receptors in the brain makes it a unique compound in neuroendocrine and sexual function research.

Key Research Features:
– Melanocortin Receptor Activity: Studied for its agonist activity at MC3R and MC4R receptors
– Sexual Function Research: Investigated for its effects on libido and arousal in laboratory models
– Central Nervous System Pathway: Explored for its CNS-mediated mechanism distinct from vascular pathways
– Neuroendocrine Studies: Associated with research on hypothalamic signaling and hormonal interaction
– Research-Grade Quality: Intended strictly for laboratory and scientific research purposes only

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Description

PT-141 (Bremelanotide) is a synthetic cyclic peptide analogue of alpha-melanocyte-stimulating hormone (α-MSH) that acts as a melanocortin receptor agonist. Unlike other compounds studied in sexual health research, PT-141 works through the central nervous system by targeting melanocortin receptors rather than the vascular system.

In laboratory research, PT-141 has been investigated for its potential effects on sexual arousal, libido, and related neurological pathways in both male and female experimental models. Its interaction with MC3R and MC4R receptors in the brain makes it a unique compound in neuroendocrine and sexual function research.

Key Research Features:
– Melanocortin Receptor Activity: Studied for its agonist activity at MC3R and MC4R receptors
– Sexual Function Research: Investigated for its effects on libido and arousal in laboratory models
– Central Nervous System Pathway: Explored for its CNS-mediated mechanism distinct from vascular pathways
– Neuroendocrine Studies: Associated with research on hypothalamic signaling and hormonal interaction
– Research-Grade Quality: Intended strictly for laboratory and scientific research purposes only

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