Formation of potent inhibitors of AChE by reaction of pyridinaldoximes with isopropyl methylphosphonofluoridate (GB)
- 1 January 1959
- journal article
- Published by Elsevier in Archives of Biochemistry and Biophysics
- Vol. 80 (1) , 211-214
- https://doi.org/10.1016/0003-9861(59)90359-5
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Pyridinium Aldoximes1The Journal of Organic Chemistry, 1958
- The Stereochemistry of Asymmetric Phosphorus Compounds. II. Stereospecificity in the Irreversible Inactivation of Cholinesterases by the Enantiomorphs of an Organophosphorus InhibitorJournal of the American Chemical Society, 1958
- Pyridine-2-Aldoxime Methiodide and Poisoning by AnticholinesterasesScience, 1957
- A specific antidote against lethal alkyl phosphate intoxication. III. Repair of chemical lesionArchives of Biochemistry and Biophysics, 1957
- A specific antidote against lethal alkyl phosphate intoxication. II. Antidotal propertiesArchives of Biochemistry and Biophysics, 1956
- 756. The reaction of oximes with isopropyl methylphosphono-fluoridate (Sarin)Journal of the Chemical Society, 1956
- A specific antidote against lethal alkylphosphate intoxicationArchives of Biochemistry and Biophysics, 1956
- A powerful reactivator of alkylphosphate-inhibited acetylcholinesteraseBiochimica et Biophysica Acta, 1955
- The mechanism of reaction between esterases and phosphorus-containing anti-esterasesDiscussions of the Faraday Society, 1955