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- W2078956743 abstract "Nowadays, the inhibition of acetylcholinesterase is one of the main pharmacological strategies for the treatment of Alzheimer’s disease. Therefore, a set of thirty-four derivatives of the diterpenoid dehydroabietylamine has been synthesized and screened in colorimetric Ellman’s assays to determine their ability to inhibit the enzymes acetylcholinesterase (AChE, from electric eel) and butyrylcholinesterase (BChE, from equine serum). A systematic variation of the substitution of dehydroabietylamides enabled an approach to analogs showing a remarkable inhibition potency for AChE. Particularly N-benzoyldehydroabietylamines 11, 12 and 13 were excellent inhibitors for AChE, showing inhibition rates comparable to standard galantamine hydrobromide." @default.
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- W2078956743 date "2011-09-01" @default.
- W2078956743 modified "2023-10-14" @default.
- W2078956743 title "The alterations in cholinesterase activity (AChE and BChE) among the frequent cellphone users and non users: A pilot study" @default.
- W2078956743 doi "https://doi.org/10.1016/j.neures.2011.07.1716" @default.
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