Korabecny_2025_J.Neurol.Sci_480_

Reference

Title : 7-substituted tacrine derivatives: Overcoming tacrine's hepatotoxicity while enhancing therapeutic potential in Alzheimer's disease - Korabecny_2025_J.Neurol.Sci_480_
Author(s) : Korabecny J , Svobodova B , Novak M , Horak M , Soukup O
Ref : Journal of the Neurological Sciences , 480 : , 2025
Abstract :

Tacrine (THA), the first FDA-approved acetylcholinesterase inhibitor for Alzheimer's disease (AD), was discontinued in 2013 due to its severe hepatotoxicity. This toxicity is largely attributed to the metabolic conversion of THA to 7-hydroxytacrine (7-OH-THA), which undergoes further transformation into a reactive quinone methide species, leading to glutathione depletion and liver damage

PubMedSearch : Korabecny_2025_J.Neurol.Sci_480_
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Related information

Inhibitor 3-Hydroxytacrine

Citations formats

Korabecny J, Svobodova B, Novak M, Horak M, Soukup O (2025)
7-substituted tacrine derivatives: Overcoming tacrine's hepatotoxicity while enhancing therapeutic potential in Alzheimer's disease
Journal of the Neurological Sciences 480 :

Korabecny J, Svobodova B, Novak M, Horak M, Soukup O (2025)
Journal of the Neurological Sciences 480 :