Dihexa vs GHK (without copper)

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

DihexaGHK (without copper)
CategoryPeptidesPeptides
Standard DoseResearch indicates 10-20 mg daily via oral or sublingual administration.Research indicates 1-3% concentration in topical formulations. Injectable dosing follows GHK-Cu protocols at 1-2 mg daily.
TimingMorning dosing preferred. Can be taken with or without food (orally active).Topical application morning and evening. Injectable in evening.
Cycle Duration2-4 week cycles with equal rest periods. Long-term safety data is extremely limited.Topical use can be ongoing indefinitely. Injectable cycles 8-12 weeks.
Evidence Levelanimal_plus_anecdotalmoderate_human
A

Dihexa

Peptides

Mechanism

Dihexa (N-hexanoic-Tyr-Ile-(6)-aminohexanoic amide) is an orally active, blood-brain barrier-permeable oligopeptide derived from angiotensin IV. It binds hepatocyte growth factor (HGF) with high affinity, inhibiting HGF dimerization and synergistically promoting c-Met receptor phosphorylation and signaling. Activation of HGF/c-Met drives procognitive effects through increased dendritic arborization, spinogenesis, and synaptogenesis via the PI3K/AKT signaling pathway. Research indicates it is approximately 10 million times more potent than BDNF for new synapse formation.

Standard Dosing

Research indicates 10-20 mg daily via oral or sublingual administration.

Timing

Morning dosing preferred. Can be taken with or without food (orally active).

Cycle Duration

2-4 week cycles with equal rest periods. Long-term safety data is extremely limited.

Side Effects

  • Headache
  • Jaw tension
  • Increased emotional sensitivity (anecdotal)
  • Potential for excessive synaptogenesis (theoretical long-term concern)

Contraindications

  • Active cancer (HGF/c-Met pathway promotes tumor growth)
  • Pregnancy and breastfeeding
  • History of cancer

Best Stacking Partners

SemaxP21NSI-189

Mechanism

GHK (glycyl-L-histidyl-L-lysine) is a naturally occurring tripeptide found in human plasma, saliva, and urine that has an extremely high affinity for copper(II) ions. Even without exogenously complexed copper, GHK rapidly chelates available copper in biological systems, making copper-free GHK functionally similar to GHK-Cu in vivo. The peptide stimulates collagen and glycosaminoglycan synthesis, modulates metalloproteinase activity, resets gene expression patterns toward a healthier state (affecting 31.2% of human genes), and activates wound healing cascades.

Standard Dosing

Research indicates 1-3% concentration in topical formulations. Injectable dosing follows GHK-Cu protocols at 1-2 mg daily.

Timing

Topical application morning and evening. Injectable in evening.

Cycle Duration

Topical use can be ongoing indefinitely. Injectable cycles 8-12 weeks.

Side Effects

  • Mild skin irritation (topical)
  • Injection site reactions

Contraindications

  • Wilson's disease
  • Pregnancy and breastfeeding

Best Stacking Partners

GHK-CuBPC-157Epitalon

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