GHRP-2

Most potent GHRP for GH release per dose. Approved in Japan as diagnostic agent for GH deficiency. Stronger than GHRP-6 with less appetite stimulation.

Normal Protocol

Advanced Protocol

Overview

Also Known As

Pralmorelin, KP-102, GHRP Kaken 100, D-Ala-D-β-Nal-Ala-Trp-D-Phe-Lys-NH2

Mechanism of Action

Potent GHS-R1a agonist. Dual mechanism: stimulates GH release via ghrelin receptor activation AND suppresses somatostatin. Synergistic with GHRH. Moderate cortisol/prolactin elevation (between GHRP-6 and ipamorelin). Less appetite stimulation than GHRP-6.

Product

Pralmorelin, KP-102, GHRP Kaken 100, D-Ala-D-β-Nal-Ala-Trp-D-Phe-Lys-NH2 vial
Dosing & Administration
Typical protocols and routes

Half-Life

15-60 minutes

Administration Routes

subcutaneousintravenous

Dosing Protocols

Average: 0.25 mg/day — reconstitute 5 mg vial with 2 mL bacteriostatic water, draw 10 units on insulin syringe (marked 1-100). Advanced: 0.5 mg/day — reconstitute 5 mg vial with 1 mL bacteriostatic water, draw 10 units on insulin syringe.
Research
Key findings and status

Key Research Findings

Approved in Japan as GHD diagnostic agent (Pralmorelin/GHRP Kaken 100). Bowers et al.: robust, reproducible GH response for GHD diagnosis. GHRP-2 + GHRH combination considered gold standard provocative test. Most potent GHRP per microgram in comparative studies.
Detailed Information

GHRP-2 (Growth Hormone Releasing Peptide-2, pralmorelin) is a synthetic hexapeptide growth hormone secretagogue that is considered the most potent GHRP for GH release per unit dose. Developed as a second-generation improvement over GHRP-6, it offers stronger GH release with less appetite stimulation, though it is less selective than ipamorelin regarding cortisol and prolactin effects.

Mechanism of Action

GHRP-2 is a potent ghrelin receptor (GHS-R1a) agonist that stimulates growth hormone release from the anterior pituitary. It acts synergistically with GHRH (additive or supraadditive effects when co-administered). GHRP-2 also stimulates GH release through suppression of somatostatin, the endogenous GH release inhibitor, creating a dual stimulatory mechanism.

Compared to GHRP-6, GHRP-2 produces stronger GH release per microgram administered. Its appetite-stimulating effect is present but notably less pronounced than GHRP-6, while still greater than ipamorelin. Cortisol and prolactin increases occur in a dose-dependent manner, falling between GHRP-6 (higher) and ipamorelin (lower) in magnitude.

Clinical Evidence

GHRP-2 has been extensively studied in clinical settings, primarily as a diagnostic tool for growth hormone deficiency. It is approved in Japan (as pralmorelin, brand name GHRP Kaken 100) as a diagnostic agent for GH secretory capacity. The GHRP-2 stimulation test is considered one of the most reliable provocative tests for diagnosing GHD.

Bowers et al. showed that IV administration of GHRP-2 at 1 mcg/kg produces a robust, reproducible GH response that can differentiate GH-deficient patients from normal subjects with high sensitivity and specificity. Combination testing with GHRP-2 + GHRH is considered the gold standard provocative test in some endocrinology protocols.

Safety & Legal

Side Effects & Warnings

Appetite increase (moderate, less than GHRP-6), water retention, cortisol and prolactin elevation (dose-dependent), flushing, dizziness, headache, injection site reactions. Generally well-tolerated at diagnostic doses.

Legal Status

Approved in Japan (Pralmorelin) for GH deficiency diagnosis. Available as research peptide.
Molecular Data
Chemical properties

Molecular Weight

817.97 g/mol

Amino Acid Sequence

D-Ala-D-β-Nal-Ala-Trp-D-Phe-Lys-NH2

Quick Facts

Class

GHRP

Research Status

Approved

Half-Life

15-60 minutes

Routes

subcutaneous
intravenous

Category

Growth Hormone Peptides