Analysis
A potent brain compound with a cautionary family history
Dihexa was developed at Washington State University from angiotensin IV, a fragment of a blood pressure hormone. It acts on the HGF and c-Met system, which helps nerve cells grow new connections. A university announcement in 2012 claimed it was about seven orders of magnitude more potent than BDNF at building those connections, a line still used in online marketing.
In rats with drug-induced memory problems, and in older rats, oral Dihexa improved performance in a water maze test (McCoy and colleagues, 2013). The research led to a company, Athira Pharma, which developed a related compound, fosgonimeton, for Alzheimer's disease. In 2024 its larger trial failed to beat placebo on the main measure of cognition and function. Dihexa itself has never been tested in people.
Our view. the rodent results are interesting, but the closest human test of the same idea did not work. Because the HGF and c-Met pathway also drives growth in some cancers, taking an untested, highly potent activator carries risks that have not been studied.
Studies and reports cited
- McCoy AT et al. Evaluation of metabolically stabilized angiotensin IV analogs as procognitive/antidementia agents. J Pharmacol Exp Ther, 2013
- Benoist CC et al. The procognitive and synaptogenic effects of angiotensin IV-derived peptides are dependent on activation of the hepatocyte growth factor/c-Met system. J Pharmacol Exp Ther, 2014
Summary of published research for general information. It is not medical advice and not a recommendation to use this substance.