Literature summary extracted from

Worek, F.; Thiermann, H.; Szinicz, L.; Eyer, P.
Kinetic analysis of interactions between human acetylcholinesterase, structurally different organophosphorus compounds and oximes (2004), Biochem. Pharmacol., 68, 2237-2248.

Inhibitors

EC Number	Inhibitors	Comment	Organism	Structure
3.1.1.7	(S-(2-diethylamino)isobutyl)methylphosphonothioate	i.e. VR, detailed analysis of inhibition kinetics	Homo sapiens
3.1.1.7	butylsarin	detailed analysis of inhibition kinetics	Homo sapiens
3.1.1.7	cyclosarin	detailed analysis of inhibition kinetics	Homo sapiens
3.1.1.7	diethyltabun	detailed analysis of inhibition kinetics	Homo sapiens
3.1.1.7	diisopropylfluorophosphate	detailed analysis of inhibition kinetics	Homo sapiens
3.1.1.7	fenamiphos	detailed analysis of inhibition kinetics	Homo sapiens
3.1.1.7	methamidophos	detailed analysis of inhibition kinetics	Homo sapiens
3.1.1.7	O-ethyl S-(2-(diisopropylamino)ethyl) methylphosphonothioate	i.e. VX, detailed analysis of inhibition kinetics	Homo sapiens
3.1.1.7	paraoxon-ethyl	detailed analysis of inhibition kinetics	Homo sapiens
3.1.1.7	paraoxon-methyl	detailed analysis of inhibition kinetics	Homo sapiens
3.1.1.7	sarin	detailed analysis of inhibition kinetics	Homo sapiens
3.1.1.7	soman	detailed analysis of inhibition kinetics	Homo sapiens
3.1.1.7	Tabun	detailed analysis of inhibition kinetics	Homo sapiens

Organism

EC Number	Organism	UniProt	Comment	Textmining
3.1.1.7	Homo sapiens	-	-	-

Source Tissue

EC Number	Source Tissue	Comment	Organism	Textmining
3.1.1.7	erythrocyte	-	Homo sapiens	-

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Release 2023.1 (January 2023)