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Growth Hormone Releasing Peptide-2
Also known as: Pralmorelin, KP-102
CAS 158861-67-7Formula C45H55N9O6PubChem CID 6918245
GHRP-2 (pralmorelin) is a synthetic hexapeptide ghrelin receptor agonist that stimulates pituitary growth hormone release. It is approved in Japan (Kaken Pharmaceutical, 2004) as a single-dose diagnostic agent for GH deficiency, but is NOT FDA-approved in the US and is research-only. Unlike ipamorelin, GHRP-2 is non-selective and modestly raises ACTH, cortisol, and prolactin.
GHRP-2 binds the ghrelin/GHS-R1a receptor on pituitary somatotrophs and in the hypothalamus, triggering Gq-coupled calcium signaling and pulsatile GH release while also suppressing somatostatin tone. At therapeutic and supratherapeutic doses it produces measurable rises in ACTH, cortisol, and prolactin (less than GHRP-6 or hexarelin, but more than ipamorelin) and stimulates appetite through ghrelin-pathway activation.
GHRP-2 is approved in Japan (Kaken Pharmaceutical, 2004) as pralmorelin for single-dose diagnostic GH-stimulation testing; Chihara et al. (2007, PMID 17609397) validated a 100 mcg IV dose with a peak-GH <15 mcg/L cut-off against the insulin tolerance test. Arvat et al. (1997, PMID 9285939) showed GHRP-2 raises GH, prolactin, ACTH, and cortisol in healthy men, with hormonal effects similar to hexarelin. Laferrère et al. (2005, PMID 15699539) demonstrated that IV GHRP-2 significantly increases food intake in healthy men, consistent with its ghrelin-like activity. Pralmorelin review: Drugs R D 2004 (PMID 15230633). GHRP-2 is more potent than ipamorelin for raw GH output but is non-selective; grey-market anti-aging, muscle-gain, and performance use is not clinically validated in the US.
Aggregated from 13 lab-verified Certificates of Analysis uploaded directly by 1 verified lab. Purity averages exclude values outside [50%, 100%] to filter unit-misreads.
COAs
13
Verified labs
1
Avg purity
99.30%
±0.49%
Endotoxin tested
54%
Tested by
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