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• W4229366237 startingPage "116807" @default.
• W4229366237 abstract "The chromane ring system is widely distributed in nature and has proven to be a highly potent pharmacophore in medicinal chemistry, which includes the area of Alzheimer's and Parkinson's diseases. We report on the development of a gem-dimethylchroman-4-ol family that was shown to give good inhibition of equine serum butyrylcholinesterase (eqBuChE) (in the range 2.9 - 7.3 μM) and in the same range of currently used drugs. We also synthesized a small library of gem-dimethylchroman-4-amine compounds, via a simple reductive amination of the corresponding chromanone precursor, that were also selective for eqBuChE presenting inhibitions in the range 7.6 - 67 μM. Kinetic studies revealed that they were mixed inhibitors. Insights into their mechanism of action were obtained through molecular docking and STD-NMR experiments, and the most active examples showed excellent drug-likeness and pharmacological properties predicted using Swiss-ADME. We also prepared a set of propargyl gem-dimethylchromanamines, for monoamine oxidase (MAO) inhibition but they were only moderately active (the best being 28% inhibition at 1 µM on MAO-B). Overall, our compounds were found to be best suited as inhibitors for BuChE." @default.
• W4229366237 created "2022-05-10" @default.
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• W4229366237 date "2022-08-01" @default.
• W4229366237 modified "2023-10-18" @default.
• W4229366237 title "Evaluation of chromane derivatives: Promising privileged scaffolds for lead discovery within Alzheimer’s disease" @default.
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• W4229366237 doi "https://doi.org/10.1016/j.bmc.2022.116807" @default.
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