4.4 Article

Azole derivatives inhibit wildtype butyrylcholinesterase and its common mutants

Journal

DRUG DEVELOPMENT RESEARCH
Volume -, Issue -, Pages -

Publisher

WILEY
DOI: 10.1002/ddr.22071

Keywords

acetylcholinesterase; butyrylcholinesterase; enzyme kinetics

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This study examined the inhibitory effects of a class of compounds called Azoles on AChE and BChE, and discovered two derivatives with strong inhibition against both wildtype and mutant BChE. Kinetic analysis and molecular modeling further supported these findings and provided insights into the inhibitory behavior of these compounds against mutant BChE forms.
Azoles, which have been used for antifungal chemotherapy for decades, have recently been of interest for their efficacy against acetylcholinesterase (AChE) and butyrylcholinesterase (BChE). There is little known about the potential of azoles against BChE, however there is none regarding their inhibitory effects against mutants of BChE. In the current study, an azole library of 1-aryl-2-(1H-imidazol-1-yl)ethanol/ethanone oxime esters were tested against AChE and BChE, which yielded derivates more potent than the positive control, galantamine, against both isoforms. Kinetic analyses were performed for wildtype and mutant (A328F and A328Y) inhibition for the two most potent BChE inhibitors, pivalic and 3-bezoylpropanoic acid esters of 2-(1H-imidazol-1-yl)-1-(2-naphthyl)ethanol, which were found to have great affinity to the wildtype and mutant BChE types with K-i values as low as 0.173 +/- 0.012 mu M. The compounds were identified to show linear competitive or mixed type inhibition. Molecular modeling confirmed these kinetic data and provided further insights regarding molecular basis of BChE inhibition by the active derivatives. Thus, current study suggests new azole derivatives with promising cholinesterase inhibitory effects and reveals the first set of information to promote our understanding for the inhibitory behavior of this class against the mutant BChE forms.

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