Design of a potent reactivator of tabun-inhibited acetyleholinesterase-synthesis and evaluation of (E)-1-(4-carbamoylpyridinium)-4-(4-hydroxyiminomethylpyridinium)-but-2-ene dibromide (K203) Article

Musilek, Kamil, Jun, Daniel, Cabal, Jiri et al. (2007). Design of a potent reactivator of tabun-inhibited acetyleholinesterase-synthesis and evaluation of (E)-1-(4-carbamoylpyridinium)-4-(4-hydroxyiminomethylpyridinium)-but-2-ene dibromide (K203) . JOURNAL OF MEDICINAL CHEMISTRY, 50(22), 5514-5518. 10.1021/jm070653r

International Collaboration

cited authors

  • Musilek, Kamil; Jun, Daniel; Cabal, Jiri; Kassa, Jiri; Gunn-Moore, Frank; Kuca, Kamil

sustainable development goals

authors

publication date

  • November 1, 2007

published in

keywords

  • ACETYLCHOLINESTERASE REACTIVATORS
  • AGENT
  • BISPYRIDINIUM COMPOUNDS BEARING
  • CHOLINESTERASE REACTIVATORS
  • CRYSTAL-STRUCTURES
  • Chemistry, Medicinal
  • LINKER
  • Life Sciences & Biomedicine
  • OBIDOXIME
  • OXIMES
  • Pharmacology & Pharmacy
  • SERIES
  • Science & Technology
  • TOXICITY

Digital Object Identifier (DOI)

publisher

  • AMER CHEMICAL SOC

start page

  • 5514

end page

  • 5518

volume

  • 50

issue

  • 22