| 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 |
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