Title : Two step synthesis of a non-symmetric acetylcholinesterase reactivator - Musilek_2007_Molecules_12_1755 |
Author(s) : Musilek K , Kuca K , Dohnal V , Jun D , Marek J , Koleckar V |
Ref : Molecules , 12 :1755 , 2007 |
Abstract :
The newly developed and very promising acetylcholinesterase reactivator (E)-1-(2-hydroxyiminomethylpyridinium)-4-(4-hydroxyiminomethylpyridinium)-but-2-e ne dibromide was prepared using two different pathways via a two-step synthesis involving the appropriate (E)-1-(4-bromobut-2-enyl)-2- or 4-hydroxyiminomethyl-pyridinium bromides. Afterwards, purities and yields of the desired product prepared by both routes were compared. Finally, its potency to reactivate several nerve agent-inhibited acetylcholinesterases was tested. |
PubMedSearch : Musilek_2007_Molecules_12_1755 |
PubMedID: 17960085 |
Musilek K, Kuca K, Dohnal V, Jun D, Marek J, Koleckar V (2007)
Two step synthesis of a non-symmetric acetylcholinesterase reactivator
Molecules
12 :1755
Musilek K, Kuca K, Dohnal V, Jun D, Marek J, Koleckar V (2007)
Molecules
12 :1755