Musilek_2008_Bioorg.Med.Chem_16_8218

Reference

Title : Monoquaternary pyridinium salts with modified side chain-synthesis and evaluation on model of tabun- and paraoxon-inhibited acetylcholinesterase - Musilek_2008_Bioorg.Med.Chem_16_8218
Author(s) : Musilek K , Kucera J , Jun D , Dohnal V , Opletalova V , Kuca K
Ref : Bioorganic & Medicinal Chemistry , 16 :8218 , 2008
Abstract :

Acetylcholinesterase reactivators are crucial antidotes for the treatment of organophosphate intoxication. Eighteen monoquaternary reactivators of acetylcholinesterase with modified side chain were developed in an effort to extend the properties of pralidoxime. The known reactivators (pralidoxime, HI-6, obidoxime, trimedoxime, methoxime) and the prepared compounds were tested in vitro on a model of tabun- and paraoxon-inhibited AChE. Monoquaternary reactivators were not able to exceed the best known compounds for tabun poisoning, but some of them did show reactivation better or comparable with pralidoxime for paraoxon poisoning. However, extensive differences were found by a SAR study for various side chains on the non-oxime part of the reactivator molecule.

PubMedSearch : Musilek_2008_Bioorg.Med.Chem_16_8218
PubMedID: 18676153

Related information

Citations formats

Musilek K, Kucera J, Jun D, Dohnal V, Opletalova V, Kuca K (2008)
Monoquaternary pyridinium salts with modified side chain-synthesis and evaluation on model of tabun- and paraoxon-inhibited acetylcholinesterase
Bioorganic & Medicinal Chemistry 16 :8218

Musilek K, Kucera J, Jun D, Dohnal V, Opletalova V, Kuca K (2008)
Bioorganic & Medicinal Chemistry 16 :8218