876385-20-5Relevant academic research and scientific papers
Isosorbide-2-carbamate esters: Potent and selective butyrylcholinesterase inhibitors
Carolan, Ciaran G.,Dillon, Gerald P.,Gaynor, Joanne M.,Reidy, Sean,Ryder, Sheila A.,Khan, Denise,Marquez, Juan F.,Gilmer, John F.
experimental part, p. 6400 - 6409 (2009/10/23)
In this study, we report the SAR and characterization of two groups of isosorbide-based cholinesterase inhibitors. The first was based directly on the clinically used nitrate isosorbide mononitrate (ISMN) retention of the 5-nitrate group and introduction of a series of 2-carbamate functionalities. The compounds proved to be potent and selective inhibitors of human plasma butyrylcholinesterase (huBuChE). In the second group, the nitrate ester was removed and replaced with a variety of alkyl and aryl esters. These generally exhibited nanomolar potency with high selectivity for BuChE over acetylcholinesterase (AChE). The most potent and selective compound was isosorbide-2-benzyl carbamate-5-benzoate with an IC50 of 4.3 nM for BuChE and > 50000 fold selectivity over human erythrocyte AChE. Inhibition with these compounds is time-dependent, competitive, and slowly reversible, indicating active site carbamylation.
