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Combined with its stability in biological fluids and resistance to many proteases, GHK-Cu represents an almost ideal therapeutic moleculesmall enough to get where it needs to go, stable enough to survive the journey, and active enough to produce meaningful biological effects once it arrives

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Subjects received intravenous DSIP (25 nmol/kg) or placebo before sleep for three consecutive nights

Of course, this kind of structure determination is very inefficient and unreliable