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MONOGRAPH No. 021
SEQUENCE
D-Ala-D-βNal-Ala-Trp-D-Phe-Lys-NH₂
MW
817.9 g/mol
CAS
158861-67-7
EU STATUS
Research only
WADA
Prohibited S2
MIN PURITY
≥98% HPLC
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Growth Hormone Axis

GHRP-2 — EU research guide.

GHRP-2 (Growth Hormone Releasing Peptide-2, Pralmorelin) is a synthetic hexapeptide ghrelin mimetic that stimulates GH release via the ghrelin receptor (GHS-R1a). It is more potent and has less appetite-stimulating effect than GHRP-6.

Last reviewed:

What is GHRP-2?

GHRP-2 is a synthetic hexapeptide that binds the ghrelin receptor (GHS-R1a) with high affinity, triggering GH release from the anterior pituitary. Unlike Ipamorelin, GHRP-2 also activates the central cortisol and prolactin axes to a moderate degree. It has a stronger GH pulse amplitude than GHRP-6 with less appetite stimulation. It was approved as Pralmorelin for GH stimulation testing in Japan.

What does the research show?

Clinical studies for GH stimulation diagnostics showed reliable and reproducible GH release. Research in cachectic states, post-surgical recovery and GH deficiency models demonstrates anabolic and protective effects. GHRP-2 has been the subject of multiple human pharmacokinetic studies establishing its GH secretion profile.

EU legal status

Not approved as a therapeutic in the EU (approved in Japan for diagnostic use only). WADA-prohibited in sport (S2). Available for laboratory research only.

WADA-prohibited (S2). Stimulates cortisol and prolactin in addition to GH. Not for human use outside authorised medical settings. This is a research compound, not a medication.
✓ PeptideCompare tracks GHRP-2 from EU vendors. Verify purity ≥98% HPLC and confirm D-amino acid configuration by appropriate analytical method.
EVIDENCE SUMMARY
STRONG
GH secretion — Reliable, reproducible GH release in human studies; used diagnostically as a GH-stimulation test.
MODERATE (ANIMAL)
Anabolic & recovery models — Animal studies in cachexia, post-surgical recovery and GH-deficiency models show anabolic and protective effects.
LIMITED
Selectivity — Also raises appetite (ghrelin pathway) and modestly cortisol and prolactin — less selective than ipamorelin.

Molecular information

Molecular formula
C45H55N9O6
Molecular weight
817.9 g/mol
CAS number
158861-67-7

Pharmacokinetics

Half-life (t½)
≈ 25.2 min
Source: GH-secretagogue reviews (~20–30 min)

Potency retained over time

Each line is one storage condition: it starts at 100% and falls as potency is lost. Above the dashed 80% line the material is considered reliable — hover for exact values.

Freezer −20 °C
36+ mo
Stable · >95% potency
Fridge 4 °C
3-4 mo
In use · after recon
Room 20 °C
10-13 days
Limited · moderate loss
Warm 37 °C+
2-3 days
Critical · rapid degradation

⚠ Estimates modelled per compound from its molecular properties (sequence length, cyclisation, oxidation- and deamidation-prone residues, light sensitivity). Indicative only — not lab-measured per batch.

GHRP-2 across EU suppliers

COA-verified EU vendors · Updated monthly

Frequently asked questions

What is GHRP-2?

GHRP-2 is a synthetic hexapeptide that binds the ghrelin receptor (GHS-R1a) with high affinity to trigger GH release from the anterior pituitary. It was approved as Pralmorelin for GH stimulation testing in Japan.

How does GHRP-2 compare to Ipamorelin and GHRP-6?

It produces a stronger GH pulse amplitude than GHRP-6 with less appetite stimulation, but unlike ipamorelin it also moderately activates the cortisol and prolactin axes.

What does the research show?

Clinical studies for GH stimulation diagnostics showed reliable, reproducible GH release, and research in cachexia, post-surgical recovery and GH-deficiency models shows anabolic and protective effects.

Does GHRP-2 raise cortisol and prolactin?

Yes, to a moderate degree, which distinguishes it from the more selective ipamorelin.

Is GHRP-2 legal in the EU?

It is not approved as a therapeutic in the EU, though it is approved in Japan for GH stimulation testing, and is sold as a research compound for laboratory use only.

Is GHRP-2 banned in sport?

Yes. It appears on the WADA prohibited list (S2).

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