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Life Sci 90:131139

Therefore, future efforts are needed to achieve greater rationalization of their design, improvement of their chemical synthesis (less laborious synthetic routes, with fewer steps, good yields, minimal waste and unwanted products), and optimization of their pharmacokinetic/pharmacodynamic profile

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A key mechanistic distinction documented in preclinical literature is Ipamorelins selectivity profile: unlike earlier GHRP compounds such as GHRP-2 and GHRP-6, Ipamorelin does not stimulate release of ACTH or cortisol in preclinical systems, making it a cleaner experimental tool for isolating GH axis effects without confounding stress hormone activation [2]

doi: 10.1016/j.bpobgyn.2023.102351