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Barendrecht et al, 2007

Currently, the dysregulation of transition metal homeostasis is recognized as a critical pathogenic element in A aggregation, particularly involving Cu 2+

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Tables 1 and 2 summarize passive membrane diffusion and active transport membrane permeability, respectively, for select small molecule NNMT inhibitors for which structure activity relationships had been previously developed.[17] 1-MNA, a product inhibitor of NNMT[12, 24, 25] exhibited no passive permeability (Table 1)

10.12998/wjcc.v3.i5.418 World J