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• W1964518576 endingPage "4881" @default.
• W1964518576 startingPage "4867" @default.
• W1964518576 abstract "Selective and nanomolar acetylcholinesterase inhibitors were obtained by connecting tri- and tetracyclic quinazolinones-previously described as moderately active and unselective cholinesterase (ChE) inhibitors-via a hydroxyl group in para position to an anilinic nitrogen with different amines linked via a three carbon atom spacer. These tri- and tetracyclic quinazolinones containing different alicyclic ring sizes and connected to tertiary amines were docked to a high-resolution hAChE crystal structure to investigate the preferred binding mode in relation to results obtained by experimental structure-activity relationships. While the 'classical orientation' locating the heterocycle in the active site was rarely found, an alternative binding mode with the basic aliphatic amine in the active center ('inverted' orientation) was obtained for most compounds. Analyses of extended SARs based on this inverted binding mode are able to explain the compounds' binding affinities at AChE." @default.
• W1964518576 created "2016-06-24" @default.
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• W1964518576 date "2014-09-01" @default.
• W1964518576 modified "2023-09-30" @default.
• W1964518576 title "Amine substitution of quinazolinones leads to selective nanomolar AChE inhibitors with ‘inverted’ binding mode" @default.
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• W1964518576 doi "https://doi.org/10.1016/j.bmc.2014.06.045" @default.
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