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The medicinal-chemistry programme that produced cagrilintide, described by Kruse and colleagues in the Journal of Medicinal Chemistry in 2021, addressed this by re-engineering the amylin backbone with structural elements borrowed from calcitonin (a related, non-aggregating peptide) and attaching a fatty-acid side chain that enables reversible binding to serum albumin [1]

Studies using human dermal papilla cells show that GHK-Cu increases proliferation, reduces caspase-3 (a key apoptosis enzyme) by roughly 43 percent, and upregulates growth factors including VEGF and basic fibroblast growth factor

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