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The primary focus of PT-141 is its ability to enhance sexual arousal. By binding predominantly to the MC-4R and MC-1R, PT-141 influences sexual function and response. This interaction with melanocortin receptors is crucial for its therapeutic effects, particularly in addressing issues related to sexual desire.
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PT-141, known generically as Bremelanotide, is a synthetic peptide that represents a significantly modified derivative of alpha-melanocyte-stimulating hormone (α-MSH). It has been explored in clinical trials as a potential treatment for hypoactive sexual desire in both men and women. This peptide functions as an agonist for the melanocortin-4 (MC-4R) and melanocortin-1 (MC-1R) receptors, making it unique among similar compounds.
The primary focus of PT-141 is its ability to enhance sexual arousal. By binding predominantly to the MC-4R and MC-1R, PT-141 influences sexual function and response. This interaction with melanocortin receptors is crucial for its therapeutic effects, particularly in addressing issues related to sexual desire.
Emerging research indicates that PT-141’s agonistic activity may extend beyond sexual arousal, hinting at a role in stimulating the immune system as well. This multifaceted action positions PT-141 as a peptide with significant therapeutic potential for various physiological and clinical challenges.
Originating from melanotan 2 (MT-2), PT-141 is part of a lineage of synthetic melanocortins. Its diverse applications highlight its importance in addressing both sexual health and broader health concerns.
PRODUCTS ARE FOR RESEARCH PURPOSES ONLY
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