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GHRP-2

Growth Hormone Releasing Peptide-2 · Pralmorelin · Hexapeptide

A 6-amino-acid synthetic growth hormone secretagogue that sits between GHRP-6 and ipamorelin in terms of selectivity. Produces strong GH release with moderate cortisol and prolactin elevation. FDA-approved in Japan as a GH deficiency diagnostic (pralmorelin).

6 amino acids
GHS-R1a agonist
Moderate selectivity
Japan FDA-approved
Diagnostic for GH deficiency
Educational content only. Not medical advice. This peptide may not be FDA-approved. Full disclaimer →
Category
GH Secretagogue
Route
SC / IV injection
Japan approval
Diagnostic (pralmorelin)
Selectivity
Moderate
Evidence
Clinical

What Is GHRP-2?

GHRP-2 (D-Ala-D-BNal-Ala-Trp-D-Phe-Lys-NH2), also known as pralmorelin, is a second-generation hexapeptide GH secretagogue. It was developed to improve upon GHRP-6's selectivity while maintaining potent GH release.

GHRP-2 is notable as the only GHRP with regulatory approval anywhere in the world — it is approved in Japan as pralmorelin for the diagnosis of growth hormone deficiency (the GHRP-2 stimulation test). Its moderate selectivity profile places it between the non-selective GHRP-6 and the highly selective ipamorelin.

Core Concept
GHRP-2 activates GHS-R1a with slightly different receptor kinetics than GHRP-6, producing strong GH release with less appetite stimulation. It still elevates cortisol and prolactin, but to a lesser degree than GHRP-6. The D-beta-naphthylalanine (D-BNal) residue at position 2 is unique to GHRP-2 and contributes to its distinct receptor interaction profile.

Structure & Sequence

GHRP-2
DADBNalAWDPheK
MW: 817.9 Da · 6 (includes non-standard D-BNal) residues
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Mechanism of Action

GHRP-2's mechanism is fundamentally the same as other GHRPs — GHS-R1a activation leading to GH release. Its improved selectivity over GHRP-6 comes from subtle differences in receptor binding kinetics due to the D-beta-naphthylalanine residue, which provides a bulkier aromatic interaction in the receptor binding pocket.

GHRP-2 Mechanism
Binds
GHS-R1a
Activates
Gq -> PLC -> Ca2+
GH release
Strong pituitary response
Moderate
cortisol/prolactin increase
Less
appetite stimulation vs GHRP-6
Result
GH release with moderate side effects

Key Mechanisms

PathwayEffectSignificance
GH releasePotent GHS-R1a agonism on somatotrophsStrong, dose-dependent GH increase
Moderate appetite effectLess ghrelin-mimetic hunger than GHRP-6More tolerable for patients not seeking appetite stimulation
Cortisol/prolactinModerate HPA axis activationLess than GHRP-6 but more than ipamorelin
GH diagnosticStandardized IV bolus test protocolApproved diagnostic for GH deficiency in Japan
Synergy with GHRHEnhanced GH release when combined with GHRH analogsCommon combination protocol in clinical use

Evidence Base

StudyDesignFindingsLevel
GH deficiency diagnosisJapanese clinical validationGHRP-2 stimulation test reliably differentiates GH-deficient from GH-sufficient subjects. Basis for Japanese regulatory approval.Level I-II
GH release comparisonClinical studiesGH release: GHRP-6 > GHRP-2 > ipamorelin. Selectivity: ipamorelin > GHRP-2 > GHRP-6.Level II
Body compositionClinical researchImproved lean mass and reduced fat mass in GH-deficient subjects over 12 weeksLevel II-III
Cortisol comparisonClinical pharmacologyGHRP-2 increased cortisol ~40% less than GHRP-6 at equipotent GH-releasing dosesLevel II

Safety & Side Effects

Cortisol elevation: Less than GHRP-6 but still present. Monitor with chronic use.

Prolactin increase: Moderate elevation. Less gynecomastia risk than GHRP-6 but not negligible.

Appetite stimulation: Present but milder than GHRP-6. Some users report moderate hunger increase.

Water retention: GH-mediated. Standard precautions as with all GH-elevating therapies.

Regulatory Status

JurisdictionStatus
JapanApproved as pralmorelin for GH deficiency diagnosis
FDANot approved
WADABanned under S2

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