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GHRP-2

Status unknown

Also known as: Pralmorelin, 158861-67-7, KP-102, D-Alanyl-3-(2-naphthalenyl)-D-alanyl-L-alanyl-L-tryptophyl-D-phenylalanyl-L-lysinamide, pralmorelina, pralmoreline, E6S6E1F19M, L-Lysinamide, D-alanyl-3-(2-naphthalenyl)-D-alanyl-L-alanyl-L-tryptophyl-D-phenylalanyl-

GHRP-2 (Pralmorelin, 158861-67-7, KP-102) is classified under ghrelin / gh secretagogues.

What the research says

Aggregated from the cited literature below. We summarize sources — we don't author claims.

GHRP-2 (also called pralmorelin and others) is described as a synthetic growth hormone-releasing peptide that mimics ghrelin and can increase plasma GH levels. Research has included diagnostic exploration for GH deficiency/hypothalamo-pituitary function and studies of appetite/food intake and downstream signaling pathways. (PMIDs: 15230633, 15699539, 9798733, 9688350)

Mechanism (as reported)

Cell and culture studies reported that GHRP-2 does not act via the human growth hormone-releasing factor (GRF) receptor in GC cells (PMID: 9798733). In cultured human acromegalic tumor cells, research concluded that GHRP-2 stimulated GH secretion mainly via a PKC pathway (with reported differences versus GHRH-related signaling) and did not act on the same receptor as GHRH on those tumor-derived somatotrophs. (PMID: 9688350)

Key findings (each cites a source)

  • Pralmorelin is described as GHRP-2 and a series of synthetic growth hormone-releasing peptides were developed; the work describes pralmorelin/GHRP-2 as orally active and synthetic, with activity related to mimicking ghrelin. (PMIDs: 15230633) [PMID 15230633]
  • Research reported that pralmorelin/GHRP-2 increased plasma GH levels in healthy subjects, while the effect was significantly lower in patients with GH deficiency; a receiver-operating characteristic analysis provided a GH peak cut-off threshold value of 15.0 microg/L for identifying GH deficiency. (PMIDs: 15230633) [PMID 15230633]
  • A human study reported that acute GHRP-2 increased food intake in lean healthy men during an ad libitum buffet meal after subcutaneous infusion, and that serum GH levels rose during infusion. (PMIDs: 15699539) [PMID 15699539]
  • In rat pituitary GC cells, research reported that GHRP-2 did not alter intracellular cAMP, [Ca2+]i, or GH secretion in cells lacking the human GRF receptor, and concluded that GHRP-2 does not act through the GRF receptor. (PMIDs: 9798733) [PMID 9798733]
  • In cultured human acromegalic tumor cells, research reported that application of GHRP-2 increased GH secretion from all tested tumor cultures and that the study concluded GHRP-2 increases GH secretion mainly via the PKC pathway (with reported differences from the effects of GHRH). (PMIDs: 9688350) [PMID 9688350]
  • In an arthritic rat model, research reported that GHRP-2 administration ameliorated external arthritis symptoms and decreased serum IL-6 levels; in vitro, peritoneal macrophage cultures exposed to GHRP-2 prevented endotoxin-induced IL-6 and decreased nitrite/nitrate release. (PMIDs: 9688350) [PMID 9688350]
  • An analytical study in an anti-doping context reported identification of a novel heptapeptide described as a glycine analogue of GHRP-2 in a seized injection vial, using liquid chromatography coupled to high-resolution tandem mass spectrometry and de novo sequencing. (PMIDs: 30051972) [PMID 30051972]

Independent test grades

No independent third-party test data is available for GHRP-2 yet. Our test grades are aggregated from Finnrick, which independently tests a subset of research peptides — many approved drugs and newer or niche compounds aren't covered.

Research literature (8)

Consolidated from PubMed — each links to the original record.

FAQ

What is GHRP-2?
GHRP-2 (Pralmorelin, 158861-67-7, KP-102) is classified under ghrelin / gh secretagogues. Research goals associated with it include gh axis support.
Is GHRP-2 FDA-approved?
The regulatory status of GHRP-2 is not established in our sources.
What does the research on GHRP-2 say?
peptideone aggregates 8 references from PubMed for GHRP-2. The summary on this page digests them with citations; we summarize sources and make no efficacy claims.
Aggregated from public sources, with attribution. Not medical advice; compounds discussed are not approved for human consumption. Last updated 2026-06-15.