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Growth Hormone Peptides

GHRP-2

GHRP-2 (Pralmorelin) is a synthetic hexapeptide GHS-R1a agonist approved in Japan for GH stimulation testing — a potent non-selective GHRP that stimulates GH alongside cortisol and prolactin.

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  • HPLC purity tested
  • COA per lot, on request
  • Lyophilized, sealed
  • US shipping, tracked
  • Japanese regulatory approval for GH stimulation testing — human pharmacokinetic data published
  • Among the most potent GHS-R1a agonists characterized — reference compound for maximal GH response research
  • Stimulates GH, cortisol, prolactin, and ACTH — appropriate for broad GHS-R1a agonism pharmacology research
  • ~15–20 minute half-life produces sharp GH pulses with clean kinetic windows
  • Synergistic with GHRH analogs for combined GH pulse amplification studies

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In your order

What ships when you order GHRP-2

  • Lyophilized vial

    Sterile-filtered, freeze-dried peptide in glass vial, sealed under inert gas.

  • Lot ID on every vial

    Printed lot ID ties this exact vial to its analytical record.

  • COA on request

    Independent third-party HPLC certificate, matched to your lot, sent on request.

  • Carrier-tracked shipping

    Shipped from a US facility with full carrier tracking and protective packaging.

The Peptific standard

Why researchers buy from Peptific instead of grey-market vendors

Peptide quality is invisible until it isn’t. Lot identity, purity, fill integrity, and chain of custody are the difference between usable research material and wasted budget.

  • Third-party HPLC tested

    Every lot is tested for identity and purity by an independent analytical lab. Certificate of Analysis available on request, tied to the exact lot you receive.

  • Lyophilized and lot-tracked

    Sterile-filtered, freeze-dried, sealed under inert gas. Each vial carries its own lot ID — full chain of custody from fill to delivery.

  • US-based fulfillment

    Orders ship from a temperature-controlled US facility with carrier tracking. No drop-shipping, no opaque overseas relay.

  • Real support, not a ticket queue

    A real person responds to research questions, lot questions, and order questions — usually same business day. No bot triage.

How it works

The GHRP-2 mechanism

GHRP-2 activates GHS-R1a (ghrelin receptor) via phospholipase C / calcium-mediated signaling, producing potent GH release. Unlike ipamorelin, GHRP-2 also significantly stimulates cortisol, prolactin, and ACTH at GH-effective doses — a non-selective GHS-R1a agonism profile useful for full GH secretagogue pharmacology research.

Compound profile

Class
Synthetic hexapeptide GHRP / GHS-R1a agonist
Amino acids
6
Molecular weight
~818 Da
Half-life
~15–20 minutes in vivo
CAS
158861-67-7
Selectivity
Non-selective — stimulates GH, cortisol, prolactin, ACTH
Clinical status
Approved in Japan for GH stimulation testing
Research category
GH secretagogue, GHS-R1a pharmacology, GH axis
Storage
Lyophilized: −20°C. Reconstituted: 2–8°C, use within 30 days

Product definition

What is GHRP-2?

GHRP-2 (Pralmorelin) is a synthetic hexapeptide GHS-R1a agonist approved in Japan for GH stimulation testing — a potent non-selective GHRP that stimulates GH alongside cortisol and prolactin.

GHRP-2 (D-Ala-D-βNal-Ala-Trp-D-Phe-Lys-NH2) is a synthetic hexapeptide developed as a potent GHS-R1a agonist, and among the first GHRPs characterized in human subjects. Kaken Pharmaceutical's regulatory approval in Japan for GH stimulation testing provides human dose-response and pharmacokinetic data that is available in the published literature — unusual for a GHRP-class compound. The compound's GH-stimulating potency is among the highest of any characterized GHRP hexapeptide. In rodent and human studies, GHRP-2 produces dose-dependent GH release with EC50 in the nanomolar range. However, the same receptor engagement that produces GH release also activates ACTH/cortisol and prolactin secretion at effective GH doses — the pharmacological property that distinguishes it from ipamorelin's selective profile and defines its utility: GHRP-2 is appropriate for full GHS-R1a agonism research; ipamorelin is appropriate for GH-isolated research.

Research audience

Who studies GHRP-2?

GHRP-2 is used by researchers studying GHS-R1a pharmacology, GH secretagogue potency comparison, ACTH/cortisol co-stimulation mechanisms, pituitary hormone co-secretion, and GH axis diagnostic testing paradigms.

Research context

What does the preclinical literature say about GHRP-2?

GHRP-2 was characterized in the early 1990s as part of the systematic development of synthetic GH secretagogues following Bowers et al.'s original discovery of the GHRP pharmacological class. Its development into a Japanese-approved GH stimulation test agent represents one of the few examples of a research GHRP reaching regulatory validation — providing a published human pharmacokinetic dataset that anchors its dose-response characterization. In comparative GHRP research, GHRP-2 serves as the 'potent non-selective' reference point against which ipamorelin's selectivity is measured. Studies directly comparing GHRP-2 and ipamorelin in the same animal models documented that ipamorelin produces equivalent or greater GH release with dramatically lower cortisol and prolactin stimulation — establishing ipamorelin's selectivity claim in the published literature. The clinical GH stimulation test use of GHRP-2 (alone and in combination with GHRH) has produced a body of human data on GH reserve assessment that is relevant to researchers studying GH deficiency mechanisms and pituitary somatotrope responsiveness.

Common questions

Why use GHRP-2 instead of ipamorelin for GH axis research?
The question is what you're studying. If GH-isolated effects are needed, ipamorelin's selectivity (no cortisol/prolactin co-stimulation) is the appropriate choice. If full GHS-R1a agonism — including the cortisol, prolactin, and ACTH components — is the research endpoint, GHRP-2 is appropriate. GHRP-2 also offers the highest GH peak output among characterized hexapeptide GHRPs, making it the tool when maximal GH response is required regardless of co-stimulation.
Is GHRP-2 approved for clinical use?
GHRP-2 is approved in Japan as a GH stimulation test agent (Kaken Pharmaceutical). It is not FDA-approved in the United States. The Japanese approval provides a human pharmacokinetic and pharmacodynamic dataset in the published literature, distinguishing it from most GHRP-class compounds which have only animal data.
Can GHRP-2 be combined with CJC-1295 Without DAC for research?
Yes — the GHRH+GHRP combination is well-studied. GHRP-2 paired with a GHRH analog produces synergistic GH release greater than either alone, consistent with the mechanistic model of GHRH priming (somatotrope recruitment) and GHRP amplification (GHS-R1a-mediated pulse enhancement). When cortisol/prolactin co-stimulation is an acceptable confound or is itself part of the study design, GHRP-2 is a valid GHRP partner for this combination.

Research Use Only

Sold for laboratory and research purposes only. Not approved for, nor intended for, human or veterinary consumption, diagnostic use, or therapeutic application. These products have not been evaluated by the Food and Drug Administration. Keep out of reach of children. For use by qualified researchers only.

Nothing on this page constitutes medical advice, a treatment recommendation, or a clinical protocol. Consult a qualified healthcare provider before making any health or treatment decisions.

By accessing this product page you confirm that you are a qualified researcher aged 18 or older and that you will use this product solely for lawful laboratory research purposes. View Research Use Policy

GHRP-2 (Pralmorelin) — GH Secretagogue Research Peptide | Peptific | Peptific