| Title : Synthesis of Bisquaternary Symmetric - X,d-Bis(2-Hydroxyiminomethylpyridinium) Alkane Dibromides and Their Reactivation of Cyclosarin-Inhibited Acetylcholinesterase - Kuca_2004_Lett.org.chem_1_ |
| Author(s) : Kuca K , Cabal J , Patocka J , Kassa J |
| Ref : Letters in Organic Chemistry , 1 , 2004 |
|
Abstract :
Preparations of the symmetric bisquaternary oximes - 1,4-bis(2-hydroxyiminomethypyridinium) butane dibromide and 1,3-bis(2-hydroxyiminomethypyridinium)propane dibromide, and their abilities to reactivate cyclosarin-inhibited acetylcholinesterase are described. Common reactivator (pralidoxime) was used as a standard for comparison of the reactivation efficacy. The first oxime seems to be very good reactivator of cyclosarin-inhibited acetylcholinesterase |
| PubMedSearch : Kuca_2004_Lett.org.chem_1_ |
| PubMedID: |
Kuca K, Cabal J, Patocka J, Kassa J (2004)
Synthesis of Bisquaternary Symmetric - X,d-Bis(2-Hydroxyiminomethylpyridinium) Alkane Dibromides and Their Reactivation of Cyclosarin-Inhibited Acetylcholinesterase
Letters in Organic Chemistry
1
Kuca K, Cabal J, Patocka J, Kassa J (2004)
Letters in Organic Chemistry
1