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To gain insight into the cellular response to FA, we obtained human pre-B lymphoblastic leukemic Nalm6 cells deficient in the FA-metabolizing enzyme ADH5 ( ADH5 ) and explored the tolerance to FA, the accumulation of the DNA double-strand break (DSB) marker -H2AX, and the phosphorylation of the tumour suppressor p53

Additionally, the gastrointestinal (GI) absorption efficiencies and bloodbrain barrier (BBB) penetration capabilities were evaluated using the BOILED-Egg classification model, which categorizes the compounds according to their predicted passive absorption and central nervous system access based on the apparent polarity (TPSA) and lipophilicity (WLOGP) values ( Results ChE inhibitory effects of the phenolic compounds As shown in Table 1, all compounds from various chemical groups were tested against 10 mM of the ChEs, of which 12 compounds were able to inhibit AChE, while 8 compounds achieved BChE inhibition over 50%

J., Mowat, A

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