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Literature summary for 3.1.1.7 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.
    View publication on PubMed

Inhibitors

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

Organism

Organism UniProt Comment Textmining
Homo sapiens
-
-
-

Source Tissue

Source Tissue Comment Organism Textmining
erythrocyte
-
Homo sapiens
-