Peptide Protocol

Hexarelin: the most potent GHRP — brief cycles only.

Synthetic hexapeptide — most potent GHRP available. Strong GH release plus unique cardioprotective effects. Short cycles essential.

Open Calculator 🌶️ All Protocols →
peppercalc.com · research use only
100–200 mcg
Per Dose
4–8 weeks on / 8 off
Cycle
SubQ
Route
2–3× daily
Frequency
Overview

What is Hexarelin?

Hexarelin is a D-2-Nal substituted analog of GHRP-6, with a single amino acid change that dramatically increases potency. It binds GHS-R1a receptors in the pituitary and hypothalamus, producing the strongest GH pulses of any GHRP at equivalent doses. It also binds CD36 receptors on cardiac myocytes, independently of GH, producing documented cardioprotective effects in preclinical models.

The downside of its potency is accelerated receptor desensitization. Hexarelin requires shorter cycles (4–8 weeks maximum) with extended off periods (8+ weeks) to preserve receptor sensitivity. Cortisol and prolactin elevation is moderate — more than Ipamorelin, less than GHRP-6. Its superior cardiac research profile and raw GH output make it a unique compound despite the shorter cycle length.

💪
GHS-R1a Potency
Most potent GHRP at GHS-R1a — produces GH pulses approximately 3× greater than GHRP-6. Activates calcium-dependent GH vesicle release via PKC pathway.
❤️
CD36 Cardioprotection
Directly binds CD36 receptors on cardiac tissue, activating eNOS and improving cardiac contractility — a unique mechanism independent of GH release.
Somatostatin Suppression
Strong hypothalamic somatostatin inhibition amplifies GH output further when co-administered with GHRH analogs.
⚠️
Rapid Desensitization
Intense GHS-R1a stimulation causes faster receptor downregulation than other GHRPs, necessitating short 4–8 week cycles with extended rests.
Dosing Protocol

Dosing Schedule

Parameters documented in published preclinical and clinical research.

⚠️ Research use only. The following documents parameters from published preclinical and clinical research. Not medical advice. Not for human consumption. Consult a licensed healthcare professional before any use.
PhaseDoseFrequencyDurationNotes
Start100 mcgOnce daily (bedtime)Days 1–7Begin conservatively. Potency means lower doses are effective.
Working dose100–200 mcg2× dailyWeeks 2–6AM fasted + bedtime. Short cycle — max 8 weeks to limit desensitization.
Advanced200 mcg3× dailyWeeks 2–6Doses above 200 mcg add minimal GH but accelerate desensitization.
Off cycle8+ weeksExtended rest is critical to restore receptor sensitivity before next cycle.
Safety Profile

Safety & Side Effects

✓ Generally Well Tolerated
Highest GH output per dose of any GHRP
Unique cardioprotective properties via CD36 binding
Well-characterized mechanism from multiple studies
Short half-life — controllable dosing
⚠ Potential Concerns
Rapid receptor desensitization — requires short cycles
Elevated cortisol and prolactin vs Ipamorelin
WADA S2 prohibited
More pronounced water retention and joint aches
⚠️
Research use onlyThis page is an educational reference. None of this constitutes medical advice. Consult a qualified professional before any use. All compounds are for research purposes only.
Evidence Base

Academic References

  1. [1]
    Laron Z, et al. (1995). Growth-enhancing effect of intranasal administration of hexarelin in children with short stature. Acta Endocrinol. 129(3):251–5. PubMed ↗
  2. [2]
    Muccioli G, et al. (2004). Hexarelin as a cardioprotective agent: structure-activity studies. Endocrinology. 145(1):257–66. PubMed ↗
  3. [3]
    Broglio F, et al. (1999). Hexarelin, a synthetic GH secretagogue, but not natural GH-releasing peptides, has a direct cardiotropic action. Eur J Endocrinol. 140(5):449–56. PubMed ↗
  4. [4]
    Torsello A, et al. (1997). Mechanism of action of Hexarelin, a synthetic growth hormone-releasing peptide. Neuroendocrinology. 65(3):205–14. PubMed ↗
Recommended Source
Source your compounds at White Market Peptides
Use code PEPPERCALC10 for 10% off + free 2-day shipping over $200
Shop Now →