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Hexarelin

Potent growth hormone releasing peptide with cardioprotective effects

Hexarelin molecular structure

WADA BANNED - Prohibited in competitive sports as potent growth hormone releasing agent

Overview

Hexarelin (Examorelin) is a synthetic hexapeptide growth hormone secretagogue that demonstrates unique dual activity: potent GH stimulation through ghrelin receptor activation and distinct cardioprotective effects through CD36 receptor binding. Research shows Hexarelin produces the strongest GH release among the GHRP family peptides, though it is subject to desensitization with prolonged use. The cardioprotective properties are independent of GH release and involve direct effects on cardiac tissue, including improved contractility, reduced apoptosis, and protection against ischemia-reperfusion injury. Studies demonstrate Hexarelin may improve cardiac function in heart failure models and protect against doxorubicin-induced cardiotoxicity. The peptide has been investigated for both growth hormone deficiency and cardiovascular applications. Like other GHRPs, Hexarelin increases appetite and produces modest elevations in cortisol and prolactin. Administration requires subcutaneous injection, and cycling protocols are often recommended to prevent receptor desensitization. The unique cardiac benefits distinguish Hexarelin from other growth hormone secretagogues.

Last reviewed: 2026-08-18

Identity & Aliases

Also known as

ExamorelinHexarelin acetateGHS-R1a agonist hexapeptideGHRP-like hexapeptide

Status: Research compound - Growth hormone agonist

CAS140703-51-1
PubChem6918245

Full composition (formula, molecular weight, sequence) in Quick Facts →

Research Areas

Growth hormone secretionGrowth hormone deficiencyHeart failure and cardiac functionAging and sarcopenia

Available Evidence

Human

Clinical studies show hexarelin stimulates GH release in a dose-dependent manner in healthy subjects, including via intranasal and oral routes without short-term desensitization, and its blunted GH response in elderly subjects can be restored by arginine/GHRH priming. Cardiotropic studies reported GH-independent improvements in cardiac function measures in patients with dilated or ischemic cardiomyopathy.

Animal

Rodent studies identified CD36 as the cardiac binding site mediating GH-independent cardiovascular actions of growth hormone-releasing peptides such as hexarelin, supporting direct cardioprotective effects beyond GH release.

In Vitro

Hexarelin acts as an agonist at the ghrelin receptor GHS-R1a, and laboratory assays demonstrate CD36 binding in cardiac tissue.

Uncertain

Clinical evidence is largely from small, short-term studies from the 1990s-2000s; long-term efficacy for muscle, aging, or cardiac outcomes is unproven, and there is no approved indication.

Key Studies & Findings

4 studies
Clinical2001

GH-independent cardiotropic activity of hexarelin observed in normal subjects, GH-deficient patients, and patients with idiopathic or ischemic dilated cardiomyopathy.

Preclinical2002

CD36 identified as the cardiac receptor site mediating the cardiovascular action of growth hormone-releasing peptides including hexarelin.

Benefits & Effects

12 documented

Muscle growth

anecdotal

Enhanced recovery

anecdotal

Improved strength

anecdotal

Fat loss

anecdotal

Anti-aging effects

anecdotal

Better sleep

anecdotal

Cardiac Performance: LVEF increased 10-14% in CAD/GHD patients

clinical

Cardiac Fibrosis Reduction: Reduces collagen, hypertrophy

clinical

Cardioprotective effects via cardiac CD36 receptor

preclinicalcardiovascular

Improved cardiac function post-myocardial infarction

preclinicalcardiovascular

Reduced visceral fat and liver triglycerides

preclinicalmetabolic

Improved insulin sensitivity

preclinicalmetabolic

Side Effects & Safety

10 reported

Appetite increase

mildcommon

ACTH/cortisol stimulation

mildcommon

Blood glucose effects

moderateuncommon

Cortisol elevation

Mild

Desensitization

Mild

Water retention

MildUncommon

Joint stiffness

MildUncommon

Appetite increase

MildUncommon

Rare prolactin-related effects

SevereRare

Mild-Moderate side effect

Mild-ModerateCommon Reversible

Onset: Hours

Management: Monitor; more pronounced than other GHRPs

Dose-dependent

Limitations & Open Questions

Most human studies are small and short-term; no large randomized trials for functional or long-term outcomes exist; effects on GH output in aging are modest and often require combination strategies; no approved therapeutic use.

Pharmacology

Hexarelin is a synthetic hexapeptide growth hormone secretagogue that agonizes the ghrelin receptor (GHS-R1a). In studies it has been given intravenously, subcutaneously, intranasally, and orally; like most peptides it is rapidly degraded, giving a short duration of action.

Reported Research Dosing

Reported values from research literature and community protocols. Educational reference only — not a dosing recommendation or medical advice.

100-300 mcg 2-3x/day

Route: SC
Half-life: 30-55 minutes

Research Protocols

GH Optimization

Dose
100 mcg
Frequency
3x daily (morning, midday, evening)
Route
SubQ

Cardioprotection Research

Dose
100-200 mcg
Frequency
2x daily
Route
SubQ

Recovery/Anti-Aging

Dose
100 mcg
Frequency
2x daily (morning and bedtime)
Route
SubQ

With GHRH (Synergistic)

Dose
100 mcg hexarelin + 100 mcg CJC-1295
Frequency
2-3x daily
Route
SubQ

Research protocols are for educational purposes only. Always consult qualified medical professionals.

Frequently Asked Questions

Is hexarelin approved for medical use?

No. It has been studied clinically for GH stimulation and cardiac function but has no approved indication and is sold only as a research compound.

How does hexarelin differ from GHRH or GH itself?

Hexarelin stimulates the ghrelin (GHS-R1a) pathway rather than the GHRH receptor, and it also has GH-independent effects such as direct cardiac actions.

Research Citations

3
The cardiovascular action of hexarelin.

Mao Y, Tokudome T, Kishimoto I (2014)

4
Hexarelin alleviates apoptosis on ischemic acute kidney injury via MDM2/p53 pathway.

Guan C, Li C, Shen X, Yang C, Liu Z, Zhang N, Xu L, Zhao L, Zhou B, Man X, Luo C, Luan H, Che L, Wang Y, Xu Y (2023)

5
Hexarelin attenuates abdominal aortic aneurysm formation by inhibiting SMC phenotype switch and inflammasome activation.

Jiang B, Wang M, Li X, Ren P, Li G, Wang Y, Wang L, Li X, Yang D, Qin L, Xin S (2022)

+ 21 more citations

Related Resources

Quick Facts

Formula

C47H58N12O6

Molecular Weight

887.04

Sequence

His-D-2MeTrp-Ala-Trp-D-Phe-Lys-NH2

Mechanism

Synthetic hexapeptide with strong GH-releasing activity

Safety Information

Research compound only. Limited human safety data available.

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