Musilek_2007_J.Enzyme.Inhib.Med.Chem_22_425

Reference

Title : Synthesis of a novel series of non-symmetrical bispyridinium compounds bearing a xylene linker and evaluation of their reactivation activity against tabun and paraoxon-inhibited acetylcholinesterase - Musilek_2007_J.Enzyme.Inhib.Med.Chem_22_425
Author(s) : Musilek K , Holas O , Kuca K , Jun D , Dohnal V , Dolezal M
Ref : J Enzyme Inhib Med Chem , 22 :425 , 2007
Abstract : Nine potential non-symmetrical xylene-bridged AChE reactivators were synthesized using modifications of currently known synthetic pathways. Their potency to reactivate AChE inhibited by the nerve agent tabun and the insecticide paraoxon together with nine symmetrical xylene-bridged compounds, was tested in vitro. Seven compounds were promising against paraoxon-inhibited AChE. Two compounds were found to be more potent against tabun-inhibited AChE than obidoxime at a concentration applicable in vivo.
ESTHER : Musilek_2007_J.Enzyme.Inhib.Med.Chem_22_425
PubMedSearch : Musilek_2007_J.Enzyme.Inhib.Med.Chem_22_425
PubMedID: 17847708

Related information

Citations formats

Musilek K, Holas O, Kuca K, Jun D, Dohnal V, Dolezal M (2007)
Synthesis of a novel series of non-symmetrical bispyridinium compounds bearing a xylene linker and evaluation of their reactivation activity against tabun and paraoxon-inhibited acetylcholinesterase
J Enzyme Inhib Med Chem 22 :425

Musilek K, Holas O, Kuca K, Jun D, Dohnal V, Dolezal M (2007)
J Enzyme Inhib Med Chem 22 :425