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GHRP-2: Research Overview — Mechanism, Research Areas & References

By the Banger Labs Research Team · Updated June 2026

GHRP-2 research peptide

Short answer: GHRP-2 (pralmorelin) is a synthetic hexapeptide and ghrelin-receptor (GHS-R1a) agonist studied as a growth hormone secretagogue in laboratory and preclinical research. This material is provided for research-use-only and educational purposes; it is not a drug and no human, therapeutic, or efficacy use is described or implied.

What is GHRP-2?

GHRP-2, also known as pralmorelin (developmental codes KP-102, GPA-748, WAY-GPA-748), is a synthetic peptide of the growth hormone-releasing peptide (GHRP) family with the sequence H-D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-NH2 (where D-2-Nal denotes D-2-naphthylalanine). It is classed as a hexapeptide (six amino-acid residues, molecular weight ~817.97) and was among the first synthetic growth hormone secretagogues described in the scientific literature. It is used in research settings as a tool compound for probing the growth hormone secretagogue / ghrelin-receptor system.

GHRP-2 — molecular structure (research illustration)

How GHRP-2 is studied

In published research, GHRP-2 acts as an agonist at the growth hormone secretagogue receptor type 1a (GHS-R1a), the same G-protein-coupled receptor bound by the endogenous peptide ghrelin, which is expressed in the anterior pituitary and hypothalamus. Receptor activation is associated in preclinical models with Gq/11–phospholipase C signaling and stimulation of growth hormone release from pituitary somatotrophs. Studies also report interactions with other signaling pathways, including opioid-receptor-linked effects observed in rodent models.

GHRP-2 — receptor & cell-signaling research illustration

Research areas

  • Studied in preclinical models as a growth hormone secretagogue acting via the GHS-R1a/ghrelin receptor
  • Investigated in animal models of pain signaling (e.g., supraspinal antinociception involving opioid receptors in mice)
  • Examined in rodent models of muscle proteolysis and catabolic/injury states (e.g., MuRF-1/MAFbx expression)
  • Used as a pharmacological tool to probe ghrelin-receptor signaling and downstream second-messenger cascades
  • Studied in endocrine research contexts as a probe of growth hormone axis physiology

These describe laboratory/preclinical research only. No therapeutic, medical, or efficacy claims are made.

GHRP-2 research in a laboratory setting

GHRP-2 specifications

Class Synthetic growth hormone-releasing hexapeptide (ghrelin/GHS-R agonist)
Form Lyophilized powder (reconstitute with bacteriostatic water)
Purity standard ≥ 99% HPLC
Certificate of Analysis Available per batch on request
Use Research use only — not for human or veterinary use

Handling & quality

GHRP-2 is held to a ≥ 99% HPLC purity standard with a Certificate of Analysis available per batch. Reconstitute with bacteriostatic water and store refrigerated; handle strictly for research. See reconstitution & storage.

GHRP-2 vial — research-grade detail

Frequently asked questions

What is GHRP-2?

GHRP-2, also known as pralmorelin (developmental codes KP-102, GPA-748, WAY-GPA-748), is a synthetic peptide of the growth hormone-releasing peptide (GHRP) family with the sequence H-D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-NH2 (where D-2-Nal denotes D-2-naphthylalanine). It is classed as a hexapeptide (six amino-acid residues, molecular weight ~817.97) and was among the first synthetic growth hormone secretagogues described in the scientific literature. It is used in research settings as a tool compound for probing the growth hormone secretagogue / ghrelin-receptor system.

Is GHRP-2 research use only?

Yes. GHRP-2 is supplied strictly for laboratory research — not for human or veterinary use, and not as a drug, food, or supplement.

Does Banger Labs provide a COA for GHRP-2?

Yes — a Certificate of Analysis (HPLC purity + mass-spec identity) is available per batch on request. See the COA Library.

References

  1. Pralmorelin (GHRP-2) — structure, peptide class, developmental codes, and ghrelin/GHS-R agonist mechanismWikipedia
  2. Ghrelin receptor agonist, GHRP-2, produces antinociceptive effects at the supraspinal level via the opioid receptor in mice (Peptides, 2014)PubMed (PMID 24607724)
  3. Ghrelin receptor agonist, GHRP-2, attenuates burn injury-induced MuRF-1 and MAFbx expression and muscle proteolysis in rats (Peptides, 2009)PubMed (PMID 19577604)
  4. Pralmorelin — drug entity record (identity, class, GHS-R1a mechanism)NCATS Inxight Drugs

Sources are provided for scientific reference and describe laboratory/preclinical research; they do not constitute medical advice or efficacy claims.

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By the Banger Labs Research Team. For research use only. Not for human or veterinary use. Not a drug, food, or cosmetic. Educational information, not medical advice.