What it is
Ipamorelin is a synthetic 5-amino-acid peptide developed in the late 1990s as a selective growth hormone secretagogue. It binds the ghrelin/GHS receptor in the pituitary to trigger growth hormone release. Unlike older GHS compounds, it does not significantly stimulate cortisol, prolactin, or aldosterone. Novo Nordisk advanced it to early clinical trials but discontinued development.
How it works
- 01
Ipamorelin selectively binds and activates the GHS-R1a receptor (the ghrelin receptor) in the anterior pituitary.
- 02
Receptor activation triggers a dose-dependent release of stored growth hormone from somatotroph cells, producing a transient GH spike.
- 03
Unlike older secretagogues (GHRP-2, GHRP-6, hexarelin), it shows minimal cross-activation of receptors that release ACTH, prolactin, or aldosterone — hence its 'clean' reputation.
- 04
Released GH stimulates hepatic IGF-1 production, which mediates many of the downstream anabolic and metabolic effects attributed to GH therapy.