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Hexarelin vs Ipamorelin: Potency Against Selectivity
Hexarelin and ipamorelin both hit the same ghrelin/GHSR receptor to release growth hormone — but they sit at opposite ends of a trade-off. Hexarelin pushes harder (and uniquely reaches the heart through CD36) at the cost of more cortisol/prolactin and faster desensitisation. Ipamorelin trades raw potency for a clean, selective pulse. Both are supplied by New-U for laboratory research only — not for human use.
Same receptor, different temperament
Both are growth-hormone secretagogues that activate GHSR-1a. Hexarelin is a potency-optimised descendant of GHRP-6, with two non-natural amino-acid substitutions that boost stability and GH-releasing strength. Ipamorelin took the opposite design path: maximum receptor selectivity , so it triggers GH without the cortisol, prolactin and hunger that the GHRP-6 lineage carries.
Side-by-side
The CD36 wrinkle
Hexarelin's standout feature isn't GH at all — it's CD36, a scavenger receptor in heart muscle involved in fatty-acid uptake and calcium handling. Hexarelin activation of cardiac CD36 underpins the cardioprotective effects reported in post-ischaemic injury models, a research angle ipamorelin simply doesn't have. If a study is about the heart rather than the GH axis, that's the differentiator.
Which to reach for
For the cleanest, most repeatable GH pulse with the fewest confounders, ipamorelin is the selective workhorse — and the reason it's the standard partner in the CJC-1295 + ipamorelin pairing. For maximum GH output or for cardiac CD36 work, hexarelin is the more potent (but less forgiving) tool. As with all GHRPs, hexarelin protocols lean on lower amounts and cycling to manage desensitisation.
Frequently Asked Questions
Is hexarelin or ipamorelin better? They trade potency for selectivity. Hexarelin releases more GH and engages cardiac CD36, but raises cortisol/prolactin and desensitises faster. Ipamorelin is cleaner and more selective. Choice depends on whether potency or a clean signal matters. Both research use only.
What is the difference between hexarelin and ipamorelin? Both are GHSR agonists. Hexarelin is the more potent, GHRP-6-derived peptide with added cardiac CD36 activity but more cortisol/prolactin and faster desensitisation; ipamorelin is selective with a strong-but-clean pulse and slower desensitisation.
Does hexarelin desensitise faster than ipamorelin? Yes — continuous higher-amount exposure downregulates the ghrelin receptor faster, so hexarelin research protocols favour lower amounts and cycling. Research context only.
What is hexarelin's CD36 effect? Hexarelin activates CD36, a cardiomyocyte scavenger receptor tied to fatty-acid uptake and calcium handling, underlying its studied cardioprotective effects in post-ischaemic models — an angle ipamorelin lacks. Preclinical finding only.
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Research-Grade Hexarelin & Ipamorelin
New-U supplies both as sealed 10-vial packs of lyophilised reference peptide, independently HPLC-verified at >99% purity by Janoshik and Freedom Diagnostics, with a per-batch Certificate of Analysis. Research use only — not for human consumption.
Research-grade · >99% HPLC purity · COA per lot
Buy Ipamorelin from New-U Research Compounds
Lab-verified by Janoshik Analytical (RP-HPLC + ESI-MS), sealed vials, discreet tracked worldwide shipping. For laboratory research use only — not for human consumption.
Premium research peptides at >99% HPLC-verified purity, third-party tested by Janoshik Analytical with a Certificate of Analysis on every lot. Shipped lab-direct, discreet and cold-chain, worldwide. For laboratory research use only.
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