Isosorbide-based cholinesterase inhibitors; replacement of 5-ester groups leading to increased stability

Gerald P. Dillon, Joanne M. Gaynor, Denise Khan, Ciaran G. Carolan, Sheila A. Ryder, Juan F. Marquez, Sean Reidy, John F. Gilmer

Full text: http://dx.doi.org/10.1016/j.bmc.2009.12.052

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Abstract

Isosorbide-2-carbamate-5-esters are highly potent and selective butyrylcholinesterase inhibitors with potential utility in the treatment of Alzheimer’s Disease (AD). They are stable in human plasma but in mouse plasma they undergo hydrolysis at the 5-ester group potentially attenuating in vivo potency. In this paper we explore the role of the 5-position in modulating potency. The focus of the study was to increase metabolic stability while preserving potency and selectivity. Dicarbamates and 5-keto derivatives were markedly less potent than the ester class. The 2-benzylcarbamate-5-benzyl ether was found to be potent (IC50 52 nM) and stable in the presence of mouse plasma and liver homogenate. The compound produces sustained moderate inhibition of mouse butyrylcholinesterase at 1 mg/kg, IP.

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