4.7 Article

NO-Donating Tacrine Hybrid Compounds Improve Scopolamine-Induced Cognition Impairment and Show Less Hepatotoxicity

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 51, Issue 24, Pages 7666-7669

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jm801131a

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A series of tacrine-NO donor hybrid compounds are synthesized and evaluated for cholinesterase inhibitor), activity, cogonition improving activity, and hepatotoxicity. The pharmacological results indicate that hybrid compounds 1, 2, and 3a potently inhibit cholinesterase in vitro and significantly improve the scopolamine-induced cognition impairment, whereas an analogue (3h) of 2 without the NO donor moiety does not. Compared to tacrine, 1 and 2 show much less hepatotoxicity. Molecular modeling studies suggest that 2 may interact with the catalytic and the peripheral anionic site of acetylcholinesterase.

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