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All three are GH secretagogues that activate the GHS-R1a receptor, but they differ in selectivity: The choice depends on the research protocol: selectivity (ipamorelin), power (GHRP-2) or orexigenic effect (GHRP-6)
You'll see that
GHK-CU is the most researched copper peptide, with extensive documentation of its gene expression effects and safety profile
The supplement and peptide space already operates with minimal regulatory oversight
H3: "They Are Both Tripeptides, So They Must Work Similarly" This assumption is incorrect
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There are no shortcuts that don't introduce risk
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