Acetylcholinesterase inhibition by the ketone transition state analog phenoxyacetone and 1-halo-3-phenoxy-2-propanones.

doi:10.1016/0006-291X(82)90679-9

Paper

Acetylcholinesterase inhibition by the ketone transition state analog phenoxyacetone and 1-halo-3-phenoxy-2-propanones.

Published Jan 29, 1982 · A. Dafforn, J. Neenan, C. Ash

Biochemical and biophysical research communications

Q1 SJR score

6

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0

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Abstract

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Study Snapshot

Phenoxyacetone and 1-halo-3-phenoxy-2-propanones are competitive acetylcholinesterase inhibitors, with 1-chloro-3-phenoxy-2-propanone protecting the enzyme against irreversible inhibition by CH3SO2F.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Acetylcholinesterase inhibition by the ketone transition state analog phenoxyacetone and 1-halo-3-phenoxy-2-propanones.

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