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It acts as a dual agonist at amylin receptors (AMY1R, AMY2R, AMY3R, formed by calcitonin receptor heterodimerized with RAMP1-3) and calcitonin receptors, with structural modifications (e.g., N-terminal fatty acid acylation, proline substitutions) preventing fibril formation, enhancing stability, and enabling once-weekly dosing via albumin binding for prolonged circulation

Some people round to the nearest whole unit, like drawing 13 units instead of 12.5, which adds 0.25 mg to the dose

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Important Safety Considerations Both GHK-Cu and AHK-Cu are research compounds without FDA approval for any indication