What is Hexarelin?
Hexarelin (INN examorelin) is a synthetic growth hormone-releasing peptide — a six-amino-acid GHRP that activates the ghrelin receptor to release a pulse of GH.[1][2] Its standout trait: it also binds CD36, giving it direct cardiac effects most GHRPs lack.[3] The catch is desensitization — the GH response fades with continuous use,[4] so it's cycled. It's not FDA-approved and is banned by WADA.
What is Hexarelin, exactly?
Hexarelin is a synthetic peptide — a chain of six amino acids (His-D-2-methyl-Trp-Ala-Trp-D-Phe-Lys) — designed to stimulate the body's own release of growth hormone. Its international name is examorelin.[2]
It belongs to the growth hormone-releasing peptide (GHRP) family — the same class as GHRP-2 and GHRP-6 — developed in the Bowers/Deghenghi/Ghigo research lineage. Like its relatives it's a growth hormone secretagogue: it prompts the pituitary to secrete GH rather than being GH itself.[2]
What makes hexarelin notable within that family is a second target. Beyond the ghrelin receptor every GHRP uses, hexarelin also binds CD36 — a scavenger receptor on heart-muscle cells — which gives it direct cardiovascular activity largely independent of growth hormone.[3] That dual identity, plus its tendency to desensitize with repeated use, is the whole story of why hexarelin is studied and discussed.
Is Hexarelin a peptide?
Yes — Hexarelin is a peptide. Specifically it's a hexapeptide: a chain of six amino acids (His-D-2-methyl-Trp-Ala-Trp-D-Phe-Lys), which is where the "hexa" in its name comes from.[2]
Several of its residues are modified or D-amino acids — mirror-image building blocks the body's enzymes break down more slowly — which makes a synthetic peptide like this more stable than a fully natural sequence. It behaves like the other research peptides in this catalog: a lyophilized powder, reconstituted before subcutaneous use.
What does Hexarelin do?
Hexarelin does two distinct things, which is what sets it apart. The actions described in the research are:
- Releases growth hormone. In humans, hexarelin produces a strong GH pulse — larger than GH-releasing hormone alone in head-to-head testing.[2]
- Acts on the heart via CD36. Independently of GH, hexarelin binds CD36 on cardiac cells and has been studied for direct cardioprotective effects — a feature emphasised for hexarelin more than other GHRPs.[3]
- Nudges other hormones. Like the GHRP class, it transiently raises cortisol and prolactin (and ACTH), though its prolactin effect is modest.[2]
- Desensitizes over time. With continuous daily use the GH response progressively declines.[4]
The honest framing: these are short-term endocrine and preclinical findings. They establish that hexarelin reliably releases GH and engages CD36 — not that self-administering it delivers any proven muscle, recovery, anti-aging or heart-disease outcome. Those popular framings are research-stage extrapolations.
How does Hexarelin work?
Hexarelin works through two receptors, which is the key to understanding it.
Hexarelin's ghrelin-receptor (GHS-R1a) pathway
The GH side runs through the growth hormone secretagogue receptor (GHS-R1a) — the receptor cloned in 1996 and later identified as ghrelin's target.[1] Activating it tells the pituitary's somatotroph cells to release stored GH, through a pathway separate from GH-releasing hormone (and one that also synergizes with it). This is the mechanism hexarelin shares with the whole GHRP family.
Hexarelin vs GHRP-2 and GHRP-6 — the CD36 difference
Where hexarelin diverges from GHRP-2 and GHRP-6 is the CD36 receptor on heart cells, which mediates direct cardiovascular effects without needing growth hormone.[3] The other practical difference is desensitization: studies of long-term daily hexarelin show the GH response attenuates over weeks (partial and reversible), which is why protocols cycle it rather than run it continuously.[4] So hexarelin is best understood as a GHRP with an extra cardiac dimension and a built-in "use-it-and-it-fades" caveat. See the GHRP-2 & GHRP-6 guide for the rest of the family.
tuned Hexarelin
For laboratory research use only · available to researchers. Specifications, pricing & Certificate of Analysis on the product page.
Hexarelin peptide benefits
The Hexarelin peptide benefits discussed in research follow from its two actions — the GH pulse and the CD36 cardiac effect:
- Growth-hormone release. A strong, reliable GH pulse in human testing, the basis of the recovery/body-composition interest.[2]
- Cardiac interest. Direct CD36-mediated cardioprotective effects in preclinical models — the feature that distinguishes hexarelin.[3]
The honest qualifier — repeated deliberately — is that the evidenced findings are the acute GH pulse in short human studies and cardiac effects in preclinical models; the muscle, fat-loss, anti-aging and heart-health claims are extrapolations, not outcomes proven for hexarelin. And because of desensitization, even the GH benefit fades on continuous use.[4] These are research findings, not promised results, and hexarelin is not an approved treatment for any of them.
What the research says about Hexarelin dosing
There is no established or approved human dose of Hexarelin — it has no approved use, and no controlled trial has set a dosing protocol. Figures circulated in peptide communities are vendor and forum conventions, not trial-derived, and remain unverified.
The one well-evidenced point about hexarelin dosing is desensitization: controlled studies show the GH response attenuates over weeks of repeated administration (partial and reversible), which is the basis for the "cycling" discussed in communities.[4]
Because Hexarelin is supplied strictly for laboratory research and is not for human consumption, this page does not provide dosing amounts, syringe measurements, reconstitution instructions, or administration guidance.
Hexarelin side effects
In the controlled studies, hexarelin was generally well tolerated short-term, but it carries the GHRP class effects plus its own quirk. The documented and reported effects are:
- Transient cortisol & prolactin rise. A class effect of the GHRPs, documented for hexarelin in human work (its prolactin effect is modest).[2]
- Desensitization. The signature hexarelin issue — the GH response progressively declines with continuous daily use (partial and reversible), which is why it's cycled.[4]
- Community-reported. Injection-site reactions, water retention and tingling — anecdotal, not trial endpoints.
The key honesty point is the same as for its GHRP siblings: there's no long-term human safety data for repeated hexarelin self-administration. The literature is short-term endocrine studies and preclinical cardiac work, not safety trials.
Is Hexarelin safe and FDA approved?
No — Hexarelin is not FDA-approved and has no marketing approval anywhere; it's handled as a research chemical. For athletes, hexarelin is explicitly named on the WADA Prohibited List — listed as "examorelin (hexarelin)" under class S2 (GH-releasing peptides), banned at all times.
How to choose Hexarelin
For a research peptide with no GMP supply chain, material quality is the dominant variable — endotoxin and impurities, not the molecule, are the realistic risks. A batch-specific Certificate of Analysis (UPLC purity, identity, endotoxin) does more for safety than any dosing convention; the absence of a recent, lot-matched CoA is itself a risk signal.
Common questions
What is Hexarelin?
What are the benefits of Hexarelin?
What is a typical Hexarelin dosage?
How is Hexarelin different from GHRP-2 and GHRP-6?
Is Hexarelin banned by WADA?
References
- Howard AD, Feighner SD, Cully DF, et al. A receptor in pituitary and hypothalamus that functions in growth hormone release. Science, 1996;273(5277):974–977. PMID 8688086. (GHS-R cloning — the ghrelin/GHRP receptor.)
- Arvat E, di Vito L, Maccagno B, et al. Effects of GHRP-2 and hexarelin, two synthetic GH-releasing peptides, on GH, prolactin, ACTH and cortisol levels in man. Peptides, 1997;18(6):885–891. PMID 9285939. (Hexarelin strong GH response; modest prolactin; cortisol/ACTH.)
- Bodart V, Febbraio M, Demers A, et al. CD36 mediates the cardiovascular action of growth hormone-releasing peptides in the heart. Circ Res, 2002;90(8):844–849. PMID 11988484. (Hexarelin's CD36 cardiac mechanism.)
- Rahim A, O'Neill PA, Shalet SM. Growth hormone status during long-term hexarelin therapy. J Clin Endocrinol Metab, 1998;83(5):1644–1649. PMID 9589671. (Desensitization over 16 weeks — partial & reversible.)
Hexarelin (examorelin) is a synthetic hexapeptide GH secretagogue acting at the ghrelin receptor (GHS-R1a) [1] to release a strong GH pulse and transiently raise cortisol/prolactin [2]; uniquely it also binds CD36 for direct cardiac effects [3], and its GH response desensitizes over weeks of daily use (partial, reversible) [4]. Not FDA-approved (no approval anywhere); WADA-prohibited as "examorelin (hexarelin)" (class S2 — verified against the 2026 Prohibited List). Muscle/anti-aging/heart claims are research-stage extrapolations; community ~100 mcg dosing and cycle lengths are vendor-derived and unverified. Not medical advice.
For research use only. Not for human consumption. This page summarises published research for educational purposes. It is not medical advice and is not intended to diagnose, treat, cure, or prevent any disease.
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