Dihexa, what the science actually shows

Dihexa is a synthetic angiotensin IV analog studied for cognitive enhancement and neuroprotection. Not FDA-approved. Evidence base: primarily animal studies; no human trial data identified.

Reported to be 10 million times more potent than BDNF at promoting synaptic connections in animal models. The gap between animal promise and human evidence is the widest in the nootropic category.

Evidence
★☆☆☆☆ Preliminary
Type
Synthetic Peptide
Structure
Modified hexapeptide

What Dihexa is

Developed by Joseph Harding at Washington State University. Stable, orally active analogue of Nle1-angiotensin IV. Named for two hexanoic acid modifications. Originally developed as potential Alzheimer's therapeutic.

Mechanism, in plain English

Enhances hepatocyte growth factor (HGF) activation of the c-Met receptor. c-Met promotes synaptogenesis, neuronal survival, and neurite outgrowth. Crosses blood-brain barrier orally and intranasally. Dramatically improves memory in animal models at picomolar concentrations.

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What the evidence shows

All evidence is preclinical. Restored cognitive function in aged rats to young-animal levels. Effective at picomolar concentrations. Rescued synaptic connectivity in Alzheimer's-like models. Published in JPET (2013). No human clinical trials conducted. No human safety data.

FDA status

Not FDA-approved. No human trials. Available only as research chemical.

Common synonyms

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

Safety and adverse-event landscape

No human safety data. HGF/c-Met pathway has cancer concerns: involved in tumor proliferation/metastasis. Oncogenic risk at cognitive enhancement doses is unknown. This is not a dismissible concern.

Frequently asked questions

Unknown. No human safety trials. The HGF/c-Met mechanism has theoretical cancer risk.
Extraordinary preclinical potency data. Potency in rats does not equal safety in humans.
None registered or published.
No. Peptexa is educational only.

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