Synthesis of a new reactivator of tabun-inhibited acetylcholinesterase
Authors:
- 1 October 2003
- journal article
- research article
- Published by Elsevier in Bioorganic & Medicinal Chemistry Letters
- Vol. 13 (20) , 3545-3547
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- The Influence of Anticholinergic Drug and Oxime Selection on the Effectiveness of Antidotal Treatment Against Tabun-Induced Poisoning in MiceActa Medica (Hradec Kralove, Czech Republic), 2002
- Modern strategies in therapy of organophosphate poisoningToxicology Letters, 1999
- Reactivating potency of obidoxime, pralidoxime, HI 6 and HLö 7 in human erythrocyte acetylcholinesterase inhibited by highly toxic organophosphorus compoundsArchives of Toxicology, 1998
- A comparison of the efficacy of HI6 and 2-PAM against soman, tabun, sarin, and VX in the rabbitToxicology Letters, 1994
- Organophosphate poisoningPharmacology & Therapeutics, 1993
- Pharmacology of HI-6, an H-series oximeCanadian Journal of Physiology and Pharmacology, 1989
- Efficacy of a combination of acetylcholinesterase reactivators, HI-6 and obidoxime, against tabun and soman poisoning of miceArchives of Toxicology, 1987
- Reactivation of nerve agent inhibited human acetylcholinesterases by HI-6 and obidoximeBiochemical Pharmacology, 1986
- HI-6: Reactivation of central and peripheral acetylcholinesterase following inhibition by soman, sarin and tabun in vivo in the ratBiochemical Pharmacology, 1982
- A specific antidote against lethal alkyl phosphate intoxication. V. Antidotal propertiesArchives of Biochemistry and Biophysics, 1957