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These are preclinical research findings, not evidence of benefit in people, and none is an approved treatment for cognitive decline

All the authors have approved the enclosed manuscript

We find that PP1 and PP2AB55 preferentially dephosphorylate phosphothreonine over phosphoserine residues and that a Pro residue at +1 reduces dephosphorylation kinetics across a large panel of peptides, consistent with recent and earlier data (Agostinis et al , 1987a

While the potential of Dihexa in improving on certain cognitive functions and models like learning and long term memory capacity is promising, it is important to note that further research is necessary to validate its efficacy and safety as cognitive enhancer in human subjects

To allow global fitting of Langmuir isotherms to determine K d values even for peptides that do not saturate, we assume that all peptides would bind PP1 at the same stoichiometry such that they would all saturate at the same final value