Musilek_2005_J.Enzyme.Inhib.Med.Chem_20_409

Reference

Title : Synthesis of a novel series of bispyridinium compounds bearing a xylene linker and evaluation of their reactivation activity against chlorpyrifos-inhibited acetylcholinesterase - Musilek_2005_J.Enzyme.Inhib.Med.Chem_20_409
Author(s) : Musilek K , Kuca K , Jun D , Dohnal V , Dolezal M
Ref : J Enzyme Inhib Med Chem , 20 :409 , 2005
Abstract :

Nine potential AChE reactivators were synthesized using a modification of currently known synthetic pathways. Their potency to reactivate AChE inhibited by insecticide chlorpyrifos was tested in vitro. 2,2'-Bis(hydroxyiminomethyl)-1,1'-(1,4-phenylenedimethyl)-bispyridinium dibromide seems to be the most potent AChE reactivator. The reactivation potency of these compounds depends on structural factors such as length of the linking chain between both pyridinium rings and position of the oxime moiety on the pyridinium ring.

PubMedSearch : Musilek_2005_J.Enzyme.Inhib.Med.Chem_20_409
PubMedID: 16335048

Related information

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Citations formats

Musilek K, Kuca K, Jun D, Dohnal V, Dolezal M (2005)
Synthesis of a novel series of bispyridinium compounds bearing a xylene linker and evaluation of their reactivation activity against chlorpyrifos-inhibited acetylcholinesterase
J Enzyme Inhib Med Chem 20 :409

Musilek K, Kuca K, Jun D, Dohnal V, Dolezal M (2005)
J Enzyme Inhib Med Chem 20 :409