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Review rat study data, NO pathway mechanisms, and safety considerations.
It engages binding sites with approximately ten times greater affinity than that of comparable NNMT inhibitors [2]
Some research also points to GHK-Cu inhibiting 5-alpha-reductase activity, the enzyme that converts testosterone to follicle-damaging DHT, though this finding is preliminary and far less established than its skin-remodeling effects
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Prakash, A, and K L Goa
How it works: Stimulates GH and IGF-1 with greater intensity, improving body composition and reducing persistent abdominal fat
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