Kuca_2004_Acta.Medica.(Hradec.Kralove)_47_107

Reference

Title : In vitro reactivation of acetylcholinesterase inhibited by cyclosarin using bisquaternary pyridinium aldoximes K005, K033, K027 AND K048 - Kuca_2004_Acta.Medica.(Hradec.Kralove)_47_107
Author(s) : Kuca K , Sevelova-Bartosova L , Krejcova-Kunesova G
Ref : Acta Medica (Hradec Kralove) , 47 :107 , 2004
Abstract :

We have tested four new bisquaternary pyridinium acetylcholinesterase (AChE; EC 3.1.1.7) reactivators - K005 (1,3-bis(2-hydroxyiminomethylpyridinium) propane dibromide), K033 (1,4-bis(2-hydroxyiminomethylpyridinium) butane dibromide), K027 (1 -(4-hydroxyiminomethylpyridinium)-3-(4-carbamoylpyridinium) propane dibromide) and K048 (1-(4-hydroxyiminomethylpyridinium)-4-(4-carbamoylpyridinium) butane dibromide) as the potential reactivators of AChE inhibited by cyclosarin. Their reactivation potencies were studied using standard in vitro reactivation test. Rat brain homogenate was used as the source of the enzyme. Oxime K033 seems to be the most potent reactivator of cyclosarin-inhibited AChE. Its reactivation potency is significantly higher than the efficacy of all other tested AChE reactivators.

PubMedSearch : Kuca_2004_Acta.Medica.(Hradec.Kralove)_47_107
PubMedID: 15446359

Related information

Reactivator K005    K027    K033    K048

Citations formats

Kuca K, Sevelova-Bartosova L, Krejcova-Kunesova G (2004)
In vitro reactivation of acetylcholinesterase inhibited by cyclosarin using bisquaternary pyridinium aldoximes K005, K033, K027 AND K048
Acta Medica (Hradec Kralove) 47 :107

Kuca K, Sevelova-Bartosova L, Krejcova-Kunesova G (2004)
Acta Medica (Hradec Kralove) 47 :107