The molecule was developed by Frank Ng's group at Monash University and Metabolic Pharmaceuticals in Australia during the 1990s and 2000s as a potential anti-obesity drug intended to isolate the lipolytic region of hGH without activating the growth hormone receptor or raising IGF-1.nnIn published preclinical work, the fragment has been shown to stimulate lipolysis, suppress lipogenesis, and modulate the beta-3 adrenergic receptor pathway in adipose tissue rather than acting through the classical hGH receptor
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When sourcing, the purity of the Ghk-cu Copper Peptide is non-negotiable, as contaminants can completely skew research outcomes
[DOI] [PubMed] [Google Scholar] 153.Fan K, Jia X, Zhou M, Wang K, Conde J, He J, Tian J, Yan X
