CJC-1295 exists in two forms in circulation — with and without the drug affinity complex — and they have very different half-lives. Product descriptions frequently do not say which, and the difference is not cosmetic.
GHRH analogues versus ghrelin mimetics: different mechanisms, conflated discussion
Adding the measurement that post #5 says would settle it.
Ipamorelin selectivity claims originate in preclinical characterisation and are reasonably well supported for what they claim: less effect on cortisol and prolactin than earlier GHRPs. Whether that translates to something clinically meaningful is a different question from whether the selectivity is real.
That holds under the stated conditions and I have stated them.
Post #15 is right about the mechanism and I think understates the practical bit.
Sermorelin and the growth hormone releasing hormone analogues depend on a functioning pituitary response, which is the mechanistic reason they behave differently in different people rather than a dosing problem.
This follows post #20 rather than contradicting it.
CJC-1295 exists in two forms in circulation — with and without the drug affinity complex — and they have very different half-lives. Product descriptions frequently do not say which, and the difference is not cosmetic.
Written quickly, so the reasoning may be tighter than the wording.
That is a cleaner way of putting what I was circling around.
A methods point on GHRH analogues versus ghrelin mimetics rather than a substantive one: if the comparison is not like for like, the difference you are measuring is the difference in method.
Sermorelin and the growth hormone releasing hormone analogues depend on a functioning pituitary response, which is the mechanistic reason they behave differently in different people rather than a dosing problem.
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