Kuca_2003_Bioorg.Med.Chem.Lett_13_3545

Reference

Title : Synthesis of a new reactivator of tabun-inhibited acetylcholinesterase - Kuca_2003_Bioorg.Med.Chem.Lett_13_3545
Author(s) : Kuca K , Bielavsky J , Cabal J , Kassa J
Ref : Bioorganic & Medicinal Chemistry Lett , 13 :3545 , 2003
Abstract :

Synthesis of a new asymmetric bisquaternary reactivator of tabun-inhibited acetylcholinesterase-1-(4-hydroxyiminomethylpyridinium)-4-(4-carbamoylpyridinium) butane dibromide is described. Reactivation potency of this oxime is compared to the currently used reactivators-pralidoxime, obidoxime and H-oxime HI-6.

PubMedSearch : Kuca_2003_Bioorg.Med.Chem.Lett_13_3545
PubMedID: 14505667

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Citations formats

Kuca K, Bielavsky J, Cabal J, Kassa J (2003)
Synthesis of a new reactivator of tabun-inhibited acetylcholinesterase
Bioorganic & Medicinal Chemistry Lett 13 :3545

Kuca K, Bielavsky J, Cabal J, Kassa J (2003)
Bioorganic & Medicinal Chemistry Lett 13 :3545