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  • GHRP-6 5MG 10MG
  • GHRP-6 5MG 10MG

GHRP-6 5MG 10MG

The peptide will be provided as lyophilized powder to ensure maximum stability.
GHRP-6 is a synthetic hexapeptide compound belonging to the family of growth hormone secretagogues (GHSs). Its core mechanism of action involves specifically binding to the growth hormone secretagogue receptor (GHSR) in the pituitary gland and peripheral tissues, thereby promoting the synthesis and secretion of growth hormone (GH). By activating intracellular signaling pathways in pituitary GH-secreting cells, GHRP-6 enhances GH release and indirectly regulates insulin-like growth factor-1 (IGF-1) levels, thereby participating in growth, development, and metabolic homeostasis. It influences appetite and energy metabolism via paracrine or autocrine mechanisms, exerting nutritional effects on muscle and bone, including promoting muscle protein synthesis and improving bone metabolism. GHRP-6 plays a positive role not only in studying growth hormone deficiency mechanisms and GH-IGF-1 axis function but is also widely applied in metabolic and muscular health research. It is used to analyze its effects on muscle mass maintenance and fat metabolism, promoting tissue repair.
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    GHRP-6 5mg

    The First-in-Human Ghrelin-Mimetic Hexapeptide  |  Foundational GHRP Family Research Tool

    His-D-Trp-Ala-Trp-D-Phe-Lys-NH₂ · SK&F 110679 Lineage · Research Use Only

    🏛 The Original GHRP

    The founding compound of the entire growth-hormone-releasing peptide class — first hexapeptide shown to stimulate GH release in humans (1991).

    🍽 Strongest Appetite Signal

    Produces the most prominent appetite stimulation of the GHRP family — a key property for ghrelin-pathway feeding research.

    🧬 Antagonist Scaffold

    The structural basis of D-Lys³-GHRP-6 — the standard ghrelin-receptor antagonist used in receptor-validation studies worldwide.

    🧊 D-Residue Stability

    D-Trp and D-Phe at positions 2 and 5 confer resistance to proteolytic degradation in research models.

    Product Overview

    GHRP-6 (Growth Hormone Releasing Peptide-6) is a synthetic hexapeptide with the sequence His-D-Trp-Ala-Trp-D-Phe-Lys-NH₂. It is the founding member of the GHRP family — a class of non-natural peptides with no structural homology to GHRH that potently stimulate somatotrope growth-hormone secretion via a specific receptor later identified as the ghrelin receptor GHS-R1a.

    GHRP-6 holds a unique place in endocrine-research history: it was the first GH-releasing peptide administered to humans, demonstrating dose-dependent GH release in healthy volunteers (1991) and synergistic action with GHRH. As a ghrelin mimetic, it also produces the strongest appetite stimulation in the GHRP family and activates the hypothalamo-pituitary-adrenal axis — properties that make it both a powerful secretagogue and a canonical tool for studying ghrelin-receptor biology, feeding circuits and HPA-axis crosstalk.

    Each vial contains 5mg of high-purity GHRP-6 as a white to off-white lyophilized powder, supplied strictly for in-vitro and laboratory research use only. 

    Specifications

    Product Name GHRP-6
    Synonyms GHRP · Growth Hormone Releasing Hexapeptide · His-D-Trp-Ala-Trp-D-Phe-Lys-NH₂
    CAS Number 87616-84-0
    Amino Acid Sequence His-D-Trp-Ala-Trp-D-Phe-Lys-NH₂ (6 residues, C-terminally amidated; single-letter HwAWfK-NH₂)
    Molecular Formula C46H56N12O6
    Molecular Weight ≈ 873.0 g/mol 
    Net Content 5 mg / vial 
    Appearance White to off-white lyophilized powder
    Purity ≥ 98% (by HPLC) 
    Solubility Soluble in water / aqueous buffer
    Storage Store lyophilized at -20°C, protected from light and moisture; refrigerate after reconstitution and use promptly 

    Historical Position: Where the GHRP Family Began

    🔬  1980s discovery — The GHRP series emerged from systematic synthetic-peptide screening; GHRP-6 (SK&F 110679 lineage) became the definitive hexapeptide of the class.

    🧑‍⚕️  1991 first-in-human milestone — GHRP was the first synthetic non-GHRH peptide shown to stimulate GH release in healthy men, and to act synergistically with GHRH — a result that opened the secretagogue field and ultimately led to identification of the ghrelin receptor (GHS-R1a, cloned 1996) and ghrelin itself (1999).

    🧪  Scaffold for pharmacological tools — the GHRP-6 sequence was subsequently modified to create D-Lys³-GHRP-6, the standard ghrelin-receptor antagonist used worldwide to validate GHS-R1a dependence in receptor and behavioral studies.

    🌳  Descendants — later GHRPs (GHRP-2, hexarelin, ipamorelin) were developed by modifying this scaffold for potency or selectivity — making GHRP-6 the reference ancestor of the whole family.

    Mechanism of Action

    Step What Happens
    1. GHS-R1a Binding GHRP-6 binds the ghrelin / growth-hormone-secretagogue receptor 1a (GHS-R1a) at pituitary and hypothalamic levels — the receptor later shown to be activated by endogenous ghrelin.
    2. GH Secretion Somatotrophs release GH in robust, dose-dependent pulses; GHRP-6 acts synergistically with GHRH, exceeding the response to either compound alone.
    3. Appetite Stimulation As a ghrelin mimetic, GHRP-6 produces the strongest food-intake stimulation of the GHRP family in animal models — a canonical phenotype for feeding-circuit research.
    4. HPA & Prolactin Activation GHRP-6 activates the hypothalamo-pituitary-adrenal axis — raising ACTH and cortisol — and elevates prolactin, mirroring ghrelin's full signaling profile. These co-stimulatory effects define first-generation GHRPs and distinguish them from selective agonists like ipamorelin.

    GHRP-6 vs GHRP-2 vs Ipamorelin

    Aspect GHRP-6 (this product) GHRP-2 Ipamorelin
    Sequence His-D-Trp-Ala-Trp-D-Phe-Lys-NH₂ D-Ala-D-2-Nal-Ala-Trp-D-Phe-Lys-NH₂ Aib-His-D-2-Nal-D-Phe-Lys-NH₂
    Family Position Founding member; first-in-human GHRP (1991) Potency reference (pralmorelin) Selectivity benchmark
    Appetite Stimulation Strongest in the family Strong Markedly weaker
    Cortisol / ACTH / Prolactin Elevated (ghrelin-like full profile) Elevated at higher doses No significant elevation
    Typical Research Use Feeding-circuit and GHS-R biology; antagonist-scaffold reference Peak-GH potency studies; diagnostic lineage Clean GH-axis protocols; dual-pathway blends

    Research Highlights

    📖 First-in-Human GH Stimulation (1991)

    The GH-releasing hexapeptide stimulated GH release in normal men and acted synergistically with GH-releasing hormone — the study that opened the secretagogue era (PubMed: 2108187).

    📖 Mallo et al., 1993 — Regulation Studies

    In-vivo GH responses to GHRP-6 characterized under controlled conditions, defining dose-response and regulation of the secretagogue response.

    📖 Ghrelin-Mimetic Feeding Effect

    GHRP-6 stimulates eating and food intake through ghrelin-receptor pathways; its appetite effect is consistently described as the most prominent in the research peptide space, stronger than ipamorelin or GHRP-2.

    📖 D-Lys³-GHRP-6 Antagonist Legacy

    Derivatives of the GHRP-6 scaffold (notably D-Lys³-GHRP-6) became the standard ghrelin-receptor antagonists, used to confirm receptor dependence in countless GHS-R1a studies — a testament to the scaffold's central role in ghrelin biology.

    Research Applications & Compliance Notes

    🍽  Feeding-circuit research — ghrelin-mimetic appetite stimulation, food-intake behavioral paradigms, satiety-pathway studies.
    🧬  GHS-R1a receptor pharmacology — agonist characterization, antagonist validation (with D-Lys³-GHRP-6), and receptor-dependence controls.
    ⚡  HPA-axis crosstalk studies — cortisol/ACTH and prolactin co-stimulation readouts versus selective agonists.
    📐  GH-secretagogue structure-activity studies — hexapeptide scaffold modifications across the GHRP family.

    Compliance note: GHRP-6 and related secretagogues fall under peptide hormones / growth factors on the WADA Prohibited List (category S2), and are established detection targets in doping control. Buyers conducting sports-related research should factor this in.

    Reconstitution & Handling

    💧  Add sterile or bacteriostatic water slowly down the side of the vial; swirl gently until fully dissolved — do not shake vigorously.
    🧪  Aliquot reconstituted solution to avoid repeated freeze-thaw cycles; label each aliquot with batch, concentration and preparation date.
    🧊  Lyophilized powder: store frozen (-20°C), protected from light and moisture; reconstituted solution: refrigerate and use within your validated stability window. 
    ⚖️  Handle with aseptic technique and appropriate PPE per your laboratory SOP.

    Quality Assurance

    ✔  Lot-specific Certificate of Analysis: HPLC purity confirmation + mass-spectrometry identity verification (expected intact mass ≈ 873 Da for the amidated hexapeptide; confirm salt form per your batch documentation). 

    ✔  Third-party batch testing documentation available upon request.

    References & Further Reading

    1. Bowers CY, et al. Growth hormone (GH)-releasing peptide stimulates GH release in normal men and acts synergistically with GH-releasing hormone. PubMed: 2108187. 1991.
    2. Mallo F, et al. Regulation of His-D-Trp-Ala-Trp-D-Phe-Lys-NH₂ (GHRP-6)-induced GH secretion. PubMed: 8510800. 1993.
    3. Petersenn S, et al. Growth hormone-releasing peptides — structure and kinetics. J Pediatr Endocrinol Metab. 1993. (First three GHRPs administered to humans: GHRP-6, GHRP-1, GHRP-2)
    4. Lengyel AMJ. Novel aspects of growth hormone-releasing peptides and ghrelin. Braz J Med Biol Res. 2006.
    5. GHRP-6 — ChemicalBook CB8421540 (CAS 87616-84-0, C₄₆H₅₆N₁₂O₆, MW 873.02).
    Disclaimer: This product is intended exclusively for in-vitro laboratory research use. It is not approved for human or animal use, is not a drug, food, cosmetic, or dietary supplement, and is not intended to diagnose, treat, cure or prevent any disease. All products are supplied strictly for research purposes only.
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