Cognitive ⏱ Half-life: Not fully characterized. Oral bioavailability confirmed in animal models.

Dihexa

Dihexa (N-hexanoic-Tyr-Ile-(6) aminohexanoic amide)

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Half-Life
Not fully characterized. Oral bioavailability confirmed in animal models.
Mol. Weight
507.63 g/mol

What is Dihexa?

Dihexa is one of the most potent synaptogenic compounds ever identified in research — an orally bioavailable peptidomimetic that promotes new synapse formation through the HGF/c-Met pathway at concentrations millions of times lower than traditional neurotrophic factors.

Research Applications

Synaptogenesis research, cognitive restoration models, HGF/c-Met signaling, Alzheimer’s disease models, and neurotrophic factor pharmacology.

Dosage Information (Research Use)

Animal research: 0.25-2 mg/kg oral or IP. Human dosing not established. Extreme potency requires careful protocol design. Research use only.

Reconstitution & Handling

Orally bioavailable — typically supplied as capsules or powder for oral administration. Can also be dissolved in DMSO for research injection protocols.

Half-Life & Pharmacokinetics

Not fully characterized. Oral bioavailability confirmed in animal models.

Reported Observations in Literature

No published toxicity data in animals at research doses. Theoretical concern about c-Met pathway activation and cell proliferation — not confirmed in published data. No human safety data exists.

Key Research References

  • McCoy AT, et al. “Evaluation of metabolically stabilized angiotensin IV analogs as procognitive/antidementia agents.” J Pharmacol Exp Ther. 2013

How Dihexa Works

Dihexa is a synthetic peptidomimetic derived from angiotensin IV that acts on hepatocyte growth factor (HGF) and its receptor c-Met. It facilitates HGF/c-Met dimerization, dramatically amplifying synaptogenic (new synapse formation) signaling. Published data describes it as approximately 10 million times more potent than BDNF at promoting new synapse connections. Orally bioavailable and blood-brain barrier permeable — unusual for a compound of this potency targeting CNS pathways.

Research Findings

Animal studies (rats with scopolamine-induced cognitive impairment) showed full restoration of cognitive function. The extreme potency of synaptogenic signaling has raised theoretical concerns about uncontrolled cell proliferation, though no tumorigenic effects have been published. Very early-stage research — no human clinical trials. The combination of oral bioavailability, BBB penetrance, and extreme potency makes it both promising and requiring careful research protocol design.

Dosage & Administration

Animal research: 0.25-2 mg/kg oral or IP. Human dosing not established. Extreme potency requires careful protocol design. Research use only.

Safety & Side Effects

No published toxicity data in animals at research doses. Theoretical concern about c-Met pathway activation and cell proliferation — not confirmed in published data. No human safety data exists.

Important: All safety information is derived from published research, primarily animal studies. No controlled human clinical trial data exists unless explicitly noted. This compound is sold for research purposes only.

Quick Facts

Sequence N-hexanoic-Tyr-Ile-(6) aminohexanoic amide (peptidomimetic)
Molecular Weight 507.63 g/mol
Half-Life Not fully characterized. Oral bioavailability confirmed in animal models.
Available Sizes 500mg (oral)
Storage Room temperature, protect from moisture and light.

Key Research References

  • McCoy AT, et al. "Evaluation of metabolically stabilized angiotensin IV analogs as procognitive/antidementia agents." J Pharmacol Exp Ther. 2013

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