Kuca_2004_J.Enzyme.Inhib.Med.Chem_19_39

Reference

Title : Reactivation of cyclosarin-inhibited rat brain acetylcholinesterase by pyridinium--oximes - Kuca_2004_J.Enzyme.Inhib.Med.Chem_19_39
Author(s) : Kuca K , Patocka J
Ref : J Enzyme Inhib Med Chem , 19 :39 , 2004
Abstract :

Cyclohexyl methylphosphonofluoridate (cyclosarin, cyclosin, GF) is a highly toxic organophosphate, which is resistant to conventional oxime therapy. To gain insight into the reactivation kinetics, rat brain acetylcholinesterase (AChE) was inhibited in vitro by cyclosarin (pH 8.0, 25 degrees C) and reactivated with 22 different pyridiniumoximes. Three compounds were shown to be superior to the other oximes: 4-carbamoyl-4'-[(hydroxyimino)methyl]-1,1'-(oxydimethylene)dipyridin-1-ium dichloride (HS-6), 4'-carbamoyl-2-[(hydroxyimino)methyl]-1,1'-(oxydimethylene)dipyridin-1-ium dichloride (HI-6), and 4'-carbamoyl-2-[(hydroxyimino)-methyl]-1,1'-(but-2-ene-1,4-diyl)dipyridin-1-ium dichloride (BI-6).

PubMedSearch : Kuca_2004_J.Enzyme.Inhib.Med.Chem_19_39
PubMedID: 15202491

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Citations formats

Kuca K, Patocka J (2004)
Reactivation of cyclosarin-inhibited rat brain acetylcholinesterase by pyridinium--oximes
J Enzyme Inhib Med Chem 19 :39

Kuca K, Patocka J (2004)
J Enzyme Inhib Med Chem 19 :39