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MUSCLE & GROWTHPEPTIDE PROFILE

Hexarelin

Also known as Examorelin, HEX

Hexarelin is one of the most potent synthetic growth hormone releasing peptides (GHRPs), producing the strongest GH release of any GHRP. It is a hexapeptide analog of GHRP-6 with a methylated tryptophan residue. Beyond GH release, it acts directly on cardiac tissue independently of GH, an effect shown acutely in one small study of coronary artery disease patients and in rodent ischemia-reperfusion models.

Last updated April 10, 2026

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Hexarelin: quick citable summary

Hexarelin is listed by PeptaHub as a muscle & growth peptide with a research only legal-status classification. The page summarizes mechanism, research context, common routes, safety notes, and references for writers and AI answer engines.

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PeptaHub. “Hexarelin: Mechanism, Research Context, Safety.” peptahub.com, 2026. https://peptahub.com/peptides/hexarelin. Licensed CC BY 4.0.

License: Creative Commons Attribution 4.0 International. Link back to https://peptahub.com/peptides/hexarelin.

SAMEAS / EXTERNAL IDS
Hexarelin CAS: 140703-51-1
QUICK ANSWER

What is Hexarelin?

Hexarelin is a potent GHRP acting at the ghrelin receptor. It also acts on the heart via CD36: one small study in 24 bypass-surgery patients found acute, non-GH-mediated improvement in cardiac performance. There are no heart failure or cardiovascular outcome trials.

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Overview

Hexarelin is one of the most potent synthetic growth hormone releasing peptides (GHRPs), producing the strongest GH release of any GHRP. It is a hexapeptide analog of GHRP-6 with a methylated tryptophan residue. Beyond GH release, it acts directly on cardiac tissue independently of GH, an effect shown acutely in one small study of coronary artery disease patients and in rodent ischemia-reperfusion models.

§ 02

Mechanism of action

Hexarelin binds to the ghrelin receptor (GHS-R1a) in the pituitary and hypothalamus, stimulating robust GH release. It also acts on the heart, where CD36 rather than GHS-R1a has been identified as the receptor mediating its cardioprotective effects. In rats, hexarelin protected cardiomyocytes from in vivo ischemia-reperfusion injury through interleukin-1 signalling. Unlike Ipamorelin, hexarelin also raises cortisol and prolactin.

§ 03

Reported study ranges

PurposeRouteReported rangeFrequency
GH release / body compositionsubcutaneous100200 mcg2-3x daily

Reported ranges are for research context only. Consult a qualified healthcare professional before using any peptide.

Convert Hexarelin research-range units

Need to convert mg to mcg, dose volume, or U-100 syringe units? The Hexarelin dose calculator is preloaded with these ranges, or use the general dose unit converter.

§ 04

Research summary

Hexarelin is a potent GH secretagogue in animals and humans, though no published trial establishes a specific fold-increase over baseline at the doses used in community protocols. Its cardiac effects have been studied in one small human study: 24 men with coronary artery disease undergoing bypass surgery received a single 2 mcg/kg intravenous dose and showed prompt increases in left ventricular ejection fraction, cardiac index and cardiac output plus reduced wedge pressure. GHRH and recombinant GH produced no such effect, indicating the response is not GH-mediated (Broglio, Eur J Pharmacol 2002). There are no heart failure trials and no cardiovascular outcome trials. Preclinical work in rats shows protection from ischemia-reperfusion injury. Tachyphylaxis with sustained GH secretagogue dosing is described in the class literature. Reported side effects include cortisol and prolactin elevation, appetite stimulation, and water retention.[1][2][3][4][5]

📄This section cites 5 peer-reviewed sources. View all references →
§ 04b

Evidence grading

Each claimed benefit is graded by the strength of available evidence. Grades reflect study quality, not effect size.

moderate
Growth hormone stimulationTorsello Eur J Endocrinol 1996 established GH-releasing activity in the rat; Sigalos and Pastuszak Sex Med Rev 2018 review summarises the human GH secretagogue data. Potent GH release is well replicated, but no published trial supports the specific fold-increase figures circulated in community sources
preliminary
Cardiac protection after ischemia-reperfusion injuryHuang Int Heart J 2017: rat in vivo ischemia-reperfusion model, protection via interleukin-1 signalling. Mao J Geriatr Cardiol 2014 review identifies CD36 as the cardiac receptor. Human data are limited to one acute study in 24 bypass-surgery patients (Broglio Eur J Pharmacol 2002); no cardiovascular outcome trials
preliminary
Tachyphylaxis (desensitization) with repeated dosingAttenuation of the GH response with sustained dosing is described for growth hormone secretagogues as a class (Sigalos and Pastuszak Sex Med Rev 2018). No published hexarelin-specific study defines the magnitude or time course
preliminary
Growth hormone deficiency diagnosisHexarelin was used as a provocative GH stimulation agent in European research settings in the 1990s. It was never adopted as an approved diagnostic, and no study establishing diagnostic accuracy is cited here
insufficient
Muscle mass and recovery in agingAnecdotal use only; no published clinical trials with muscle mass or functional outcomes as primary endpoints

Strong = multiple RCTs · Moderate = limited trials or observational · Preliminary = animal or in vitro only · Insufficient = anecdotal or no published data

§ 05

Side effects

Increased cortisol
Increased prolactin
Water retention
Appetite stimulation
Flushing
Injection site pain

Side effects vary by individual. This is not an exhaustive list. Report unusual symptoms to a healthcare professional.

§ 06

Common stacks

Peptides commonly paired with Hexarelin for synergistic effects.

§ 08

Sourcing & access

Research compound

Hexarelin is classified as a research compound. Regulatory status varies by jurisdiction. Always verify current legal status and source from vendors providing third-party certificates of analysis (COA).

§ 09

Frequently asked questions

Hexarelin (Examorelin) is a synthetic hexapeptide growth hormone releasing peptide and one of the more potent GHRPs. It also has direct cardiac effects that are independent of growth hormone, mediated through the CD36 receptor.

Hexarelin is described as the more potent GH releaser but, unlike Ipamorelin, it also raises cortisol and prolactin. No published head-to-head trial quantifies the difference in GH output between the two, so the fold-increase figures circulated in community sources are not sourced.

The human evidence is one small study: 24 men with coronary artery disease undergoing bypass surgery received a single 2 mcg/kg intravenous dose and showed a prompt rise in ejection fraction, cardiac index and cardiac output, and a fall in wedge pressure. GHRH and recombinant GH did not do this, so the effect is not GH-mediated. There have been no heart failure trials, and no trials of repeated dosing or clinical outcomes.

Attenuation of the GH response with sustained dosing is described for growth hormone secretagogues as a class. No published hexarelin study defines the time course, so the 4-to-8-weeks-on, 4-weeks-off cycling used in community protocols is a convention rather than a trial-derived schedule.

Community protocols use 100 to 200 mcg injected subcutaneously 2 to 3 times daily on an empty stomach. These are user-reported ranges, not trial-derived: the published human hexarelin work used single intravenous doses. Cortisol and prolactin elevation is a documented effect of hexarelin, and cycling is a community convention intended to limit receptor desensitization.

§ 10

Research references

  1. The cardiovascular action of hexarelinMao Y, Tokudome T, Kishimoto IJournal of Geriatric Cardiology, 2014Review
  2. Effects of acute hexarelin administration on cardiac performance in patients with coronary artery disease during by-pass surgeryBroglio F, Guarracino F, Benso A, Gottero C, et al.European Journal of Pharmacology, 2002PubMed
  3. The Growth Hormone Secretagogue Hexarelin Protects Rat Cardiomyocytes From in vivo Ischemia/Reperfusion Injury Through Interleukin-1 Signaling PathwayHuang J, Li Y, Zhang J, Liu Y, et al.International Heart Journal, 2017PubMed
  4. Mechanism of action of Hexarelin. I. Growth hormone-releasing activity in the ratTorsello A, Grilli R, Luoni M, Guidi M, et al.European Journal of Endocrinology, 1996PubMed
  5. The Safety and Efficacy of Growth Hormone SecretagoguesSigalos JT, Pastuszak AW.Sexual Medicine Reviews, 2018PubMed
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