Public educational draft · 04 November 2026Clinical review pending →
GHRP-2 / pralmorelin reference card with source-verified molecular imagery and original research-informed diagrams. Evidence levels and limitations are marked; full citations accompany the card on the website.

Visual summary only. The research findings, limitations and references accompany the card on this page.

The chemical drawing shows source-verified two-dimensional connectivity and stereochemistry, not an experimental three-dimensional conformation. The biological setting is an illustration. Original study diagrams summarize cited research without reproducing publication artwork or inventing quantitative results.

Verified chemical reference record

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GH axis

GHRP-2 / pralmorelin

Ghrelin receptor / GHSR

Pralmorelin peptide parent with C-terminal amide
Molecular formula
C45H55N9O6
Molecular weight
818 g/mol
Class
Synthetic hexapeptide
Identity
D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-NH2

Research snapshot

GHRP-2, also called pralmorelin, is a synthetic ghrelin-receptor agonist used in endocrine research. Acute human experiments have examined growth-hormone release and food intake.

Small human physiology experiment

Identity & representation

Literature reference molecule. Catalog naming is not analytical confirmation of AXON contents, salt, purity or formulation. D-2-Nal = D-2-naphthylalanine. Ala3, Trp4 and Lys6 are L. Distinct from GHRP-6.

Educational reference only. Not a dosing guide, treatment recommendation or product endorsement.

Stereodefined hexapeptide parent · C-terminal amide[3]

View the chemical structure →

Sources checked: 2026-11-06. Identity and evidence limits are stated above. Independent specialist review is pending.

ClassSynthetic hexapeptide

Target / pathwayGhrelin receptor / GHSR

Selected evidenceSmall human physiology experiment

ScopeResearch summary; not a product or treatment assessment

What researchers study

GHRP-2, also called pralmorelin, is a synthetic ghrelin-receptor agonist used in endocrine research. Acute human experiments have examined growth-hormone release and food intake.

  • Growth-hormone secretagogue receptor pharmacology

  • Appetite and energy intake in controlled human experiments

  • Separation of acute endocrine effects from clinical outcomes

Mechanism in context

  1. Activates the growth-hormone secretagogue receptor
  2. Produces acute endocrine and appetite-related responses
  3. Human physiology studies measure GH and meal intake

Acute hormone and meal-intake responses do not establish long-term functional benefit or safety.

Simplified publication-grounded schematic, not a solved protein structure or proof of clinical benefit.

Selected evidence

Selected human evidence is summarized above; this is not an exhaustive clinical or regulatory review.

Growth hormone releasing peptide-2 (GHRP-2), like ghrelin, increases food intake in healthy men.[1]

Small randomized double-blind crossover experiment · Lean healthy men · 270-minute experimental sessions · Reported n: 7

Observed: Participants ate more during GHRP-2 exposure and had increased GH release versus saline.

Limit: A seven-person acute experiment cannot establish sustained body-composition benefit or long-term safety.

Reference identity in detail

Sequences and form distinctions describe the cited reference substance, not a verified supplier preparation.

Read the sequence and form notes
Sequence
D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-NH2
Sequence notes
D-2-Nal = D-2-naphthylalanine. Ala3, Trp4 and Lys6 are L. Distinct from GHRP-6.
Molecular formula
C45H55N9O6
Molecular weight (g/mol)
818

Safety & evidence limits

  • The selected study measured food intake and growth hormone, not durable muscle gain, fat loss or improved health.

  • Results from seven healthy men do not establish responses across sexes, ages, disease states or prolonged exposure.

  • GHRP-2 and GHRP-6 have different sequences; their properties and findings cannot be treated as identical.

Practical identity notes

  • D-2-Nal = D-2-naphthylalanine. Ala3, Trp4 and Lys6 are L. Distinct from GHRP-6.
  • Formula and mass apply only to the named reference form, excluding unspecified counterions, solvent and water.
  • Educational molecular reference • Selected studies, not a systematic review • No dosing guidance

The 10-second takeaway

A ghrelin-receptor research peptide with acute human endocrine and appetite findings, not established long-term body-composition benefit.

What the visual panels show

Original diagrams summarize the cited research or documented evidence search. They are not copied publication figures or claims of treatment benefit.

  • ACUTE ENDOCRINE RESEARCH[1]

    Publication-grounded mechanism schematic · Original publication-grounded diagram

    Engage the growth-hormone secretagogue pathway · Measure GH during controlled experimental sessions · Compare meal intake with saline exposure

    Interpretation: Acute physiology is not durable functional benefit.

  • Acute GH response[1]

    HUMAN CROSSOVER STUDY · Original publication-grounded diagram

    GH release increased versus saline

    Seven lean healthy men; acute sessions.

    Interpretation: Hormone-response schematic only; no fabricated time curve or long-term benefit.

  • Measured meal intake[1]

    SAME HUMAN STUDY · Original publication-grounded diagram

    Participants ate more during GHRP-2 exposure

    Randomized double-blind crossover; 270-minute sessions.

    Interpretation: Meal intake is the measured endpoint, not a body-composition or health improvement.

  • Other endocrine responses[2]

    ANIMAL COMPARISON · Original publication-grounded diagram

    ACTH and cortisol also increased in swine

    Comparative secretagogue assay; not human risk estimates.

    Interpretation: Retain species and endocrine caveat. Do not label GHRP-2 selectively GH-only.

Follow the evidence

Sources & what they support

  1. Growth hormone releasing peptide-2 (GHRP-2), like ghrelin, increases food intake in healthy men.

    J Clin Endocrinol Metab · 2005 · PMID: 15699539 · DOI: 10.1210/jc.2004-1719

    Supports: Human GH and food-intake physiology

  2. Ipamorelin, the first selective growth hormone secretagogue.

    Eur J Endocrinol · 1998 · PMID: 9849822 · DOI: 10.1530/eje.0.1390552

    Supports: Comparative preclinical secretagogue hormone responses

  3. PubChem CID 6918245

    Supports: Reference chemical graph, formula and molecular mass; not product identity

    Original structure record · Download source SDF

    Original PubChem 2D source structure record.

Source-linked educational drafts. Scientific and clinical review is pending. These cards describe molecules and study context, not product quality, approval or treatment recommendations.

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