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Collect. Czech. Chem. Commun. 1975, 40, 1794-1800
https://doi.org/10.1135/cccc19751794

Kinetic and thermodynamic parameters of reactivation of O-isopropyl-methylphosphonylated rat brain acetylcholinesterase by asymmetric bis-quaternary 4-pyridine aldoximes

J. Patočka and J. Bielavský

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  • Cabal Jiri, Kuca K., Kassa J.: Specification of the Structure of Oximes Able to Reactivate Tabun-Inhibited Acetylcholinesterase. Pharmacol Toxicol 2004, 95, 81. <https://doi.org/10.1111/j.1742-7843.2004.950207.x>
  • Kuča Kamil, Bielavský Jiřı́, Cabal Jiřı́, Bielavská Marcela: Synthesis of a potential reactivator of acetylcholinesterase—1-(4-hydroxyiminomethylpyridinium)-3-(carbamoylpyridinium)propane dibromide. Tetrahedron Letters 2003, 44, 3123. <https://doi.org/10.1016/S0040-4039(03)00538-0>
  • Kuča Kamil, Bielavský Jiřı́, Cabal Jiřı́, Kassa Jiřı́: Synthesis of a new reactivator of tabun-inhibited acetylcholinesterase. Bioorganic & Medicinal Chemistry Letters 2003, 13, 3545. <https://doi.org/10.1016/S0960-894X(03)00751-0>
  • Kassa J., Cabal J.: A comparison of the efficacy of a new asymmetric bispyridinium oxime BI-6 with currently available oximes and H oximes against soman by in vitro and in vivo methods. Toxicology 1999, 132, 111. <https://doi.org/10.1016/S0300-483X(98)00146-2>
  • Kassa Jiří, Cabal Jiří: A Comparison of the Efficacy of Acetylcholinesterase Reactivators against Cyclohexyl Methylphosphonofluoridate (GF Agent) by in vitro and in vivo Methods. Pharmacology & Toxicology 1999, 84, 41. <https://doi.org/10.1111/j.1600-0773.1999.tb02109.x>
  • Kassa J, Cabal J: A comparison of the efficacy of a new asymmetric bispyridinium oxime BI-6 with presently used oximes and H oximes against sarin by in vitro and in vivo methods. Hum Exp Toxicol 1999, 18, 560. <https://doi.org/10.1191/096032799678845106>