Humanin vs Ipamorelin

Side-by-side comparison of mechanisms, dosing, interactions, and stacking potential.

HumaninIpamorelin
CategoryPeptidesPeptides
Standard DoseResearch indicates dosing remains experimental. Animal studies use 1-10 mcg/day equivalents. Human protocols are not established.Research indicates 200-300 mcg administered 1-3 times daily via subcutaneous injection.
TimingNo established timing protocol. Morning dosing suggested for neuroprotective applications.Best administered at bedtime for synergy with natural GH peak. Also effective upon waking and post-workout. Always on empty stomach.
Cycle DurationExperimental — no established cycle lengths.12-24 week cycles with 4-8 week breaks.
Evidence Levelanimal_plus_anecdotalmoderate_human
A

Humanin

Peptides

Mechanism

Humanin is a 24-amino acid mitochondrial-derived peptide encoded by the 16S rRNA gene of mitochondrial DNA. It binds IGFBP-3 with high affinity (via Phe-6), interfering with IGFBP-3 binding to importin-beta and suppressing IGFBP-3-mediated apoptosis. It also inhibits the pro-apoptotic protein Bax (Bcl-2 family), preventing mitochondrial outer membrane permeabilization and intrinsic apoptosis. Humanin and IGFBP-3 synergistically protect neurons from amyloid-beta-induced apoptosis, and it activates the STAT3 and ERK1/2 pathways for cytoprotection.

Standard Dosing

Research indicates dosing remains experimental. Animal studies use 1-10 mcg/day equivalents. Human protocols are not established.

Timing

No established timing protocol. Morning dosing suggested for neuroprotective applications.

Cycle Duration

Experimental — no established cycle lengths.

Side Effects

  • Limited data on side effects in humans
  • Theoretical: interference with normal apoptotic processes

Contraindications

  • Active cancer (anti-apoptotic effects could support tumor survival)
  • Pregnancy and breastfeeding

Best Stacking Partners

MOTS-cEpitalonSS-31
B

Ipamorelin

Peptides

Mechanism

Ipamorelin is a pentapeptide (Aib-His-D-2-Nal-D-Phe-Lys-NH2) that acts as the first selective growth hormone secretagogue receptor (GHS-R1a/ghrelin receptor) agonist. Unlike other GHRPs, it selectively stimulates GH release without significantly affecting ACTH, cortisol, prolactin, or aldosterone — even at doses 200-fold above the ED50 for GH release. This selectivity profile is comparable to GHRH itself but operates through the distinct ghrelin receptor on pituitary somatotrophs.

Standard Dosing

Research indicates 200-300 mcg administered 1-3 times daily via subcutaneous injection.

Timing

Best administered at bedtime for synergy with natural GH peak. Also effective upon waking and post-workout. Always on empty stomach.

Cycle Duration

12-24 week cycles with 4-8 week breaks.

Side Effects

  • Head rush post-injection
  • Mild hunger increase (less than GHRP-6)
  • Water retention (mild)
  • Tingling in extremities
  • Injection site irritation

Contraindications

  • Active cancer
  • Diabetic retinopathy
  • Pregnancy and breastfeeding

Best Stacking Partners

CJC-1295 (no DAC)BPC-157TB-500

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