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Ipamorelin
MetabolicKRS-IPA-10

Ipamorelin

A pentapeptide ghrelin receptor agonist and selective GH secretagogue. Studied for its targeted GH-releasing properties with minimal impact on cortisol, prolactin, or appetite signaling compared to earlier secretagogues.

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Mechanism of Action

Ipamorelin is a pentapeptide (Aib-His-D-2-Nal-D-Phe-Lys-NH2) that selectively agonizes the ghrelin receptor (GHS-R1a) on pituitary somatotrophs. Developed by Novo Nordisk from the GHRP-1 scaffold, it was the first GHRP-receptor agonist with GH-release selectivity comparable to GHRH. Unlike GHRP-6 or GHRP-2, it produces GH release without meaningful stimulation of ACTH, cortisol, prolactin, FSH, LH, or TSH, even at doses >200x the ED50 for GH release.

Research References

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01

Raun K et al. Ipamorelin, the first selective growth hormone secretagogue. Eur J Endocrinol. 1998. PMID: 9849822

02

Gobburu JV et al. Pharmacokinetic-pharmacodynamic modeling of ipamorelin, a growth hormone releasing peptide, in human volunteers. Pharm Res. 1999

03

Johansen PB et al. Ipamorelin, a new growth-hormone-releasing peptide. Pharmacological studies

04

Beck DE et al. Prospective, Randomized, controlled proof of concept study of the Ghrelin mimetic ipamorelin for the management of postoperative ileus in bowel resection patients. Int J Colorectal Dis. 2014

Batch History & Certificates of Analysis

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For Research Use Only. This product is supplied exclusively for in vitro research, laboratory study, and experimental purposes. It is not a drug, supplement, food, or cosmetic, and is not intended for human or veterinary use. See our Compliance & RUO Policy.