Dihexa Protocol
Dosing & Research
Last Updated: September 4, 2026
Also known as: PNB-0408, N-hexanoic-Tyr-Ile-(6)-aminohexanoic amide
- Amino Acid Sequence
- N-hexanoic-Tyr-Ile-(6)-aminohexanoic amide
- Molecular Formula
- C27H44N4O5
- Molecular Weight
- 504.67 g/mol
- CAS Number
- 1401708-83-5
Synaptogenesis and dendritic-spine formation research, HGF/c-Met pathway modulation studies, Animal cognitive/memory models, Oral angiotensin IV analog pharmacology
How It Works
- Orally active angiotensin IV analog originally proposed to positively modulate the HGF/c-Met signaling pathway, promoting dendritic spine formation and synaptogenesis in animal neuron models. Caution: the foundational mechanism papers from the originating laboratory (Kawas, Wright, Harding et al.) were formally retracted in April 2025 following a Washington State University research-misconduct investigation that found falsified/fabricated image data, so the HGF/c-Met mechanism should be treated as unconfirmed pending independent replication.
- Synaptogenesis and dendritic-spine formation research
- HGF/c-Met pathway modulation studies
- Animal cognitive/memory models
- Oral angiotensin IV analog pharmacology
Dosing Structure
Example Protocols
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What Is Dihexa?
Dihexa (PNB-0408) is an orally active, synthetic angiotensin IV analog studied in rodent models for its proposed ability to promote synaptogenesis and dendritic spine formation. It is not derived from an approved drug and has zero completed human clinical trials. Critically, the foundational laboratory papers describing its HGF/c-Met mechanism were formally retracted in April 2025 after a university investigation found falsified image data, so the evidence base behind Dihexa should be treated with significant caution pending independent replication.
- ▸Origin: Dihexa emerged from an angiotensin IV analog research program at Washington State University aimed at developing orally bioavailable cognition-enhancing compounds.
- ▸Proposed mechanism: The compound was reported to positively modulate the hepatocyte growth factor (HGF)/c-Met signaling pathway, promoting dendritic spine formation and synaptogenesis in cultured neurons and rodent cognitive models.
- ▸Retraction (April 2025): Following a Washington State University research-misconduct investigation, the foundational 2012 mechanism paper (Kawas, McCoy, Yamamoto, Wright, Harding -- J Pharmacol Exp Ther) and a related paper describing Dihexa's procognitive/synaptogenic effects were formally retracted after the investigation found altered/fabricated image data in the first author's dissertation and co-authored papers.
- ▸No human data: There are no completed, registered human clinical trials evaluating Dihexa's safety, pharmacokinetics, or cognitive effects.
Evidence Summary
Research & Studies
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