Tetroxime: reactivation potency - in vitro and in silico study

被引:4
作者
Kuca, K. [1 ,2 ,3 ]
Korabecny, J. [1 ,4 ]
Dolezal, R. [1 ]
Nepovimova, E. [1 ,4 ]
Soukup, O. [1 ]
Gorecki, L. [1 ,4 ]
Musilek, K. [1 ,2 ,4 ]
机构
[1] Univ Hosp Hradec Kralove, Biomed Res Ctr, Hradec Kralove, Czech Republic
[2] Univ Hradec Kralove, Fac Sci, Dept Chem, Hradec Kralove, Czech Republic
[3] Florida Int Univ, Herbert Wertheim Coll Med, Dept Cellular Biol & Pharmacol, Miami, FL 33199 USA
[4] Univ Def, Fac Mil Hlth Sci, Dept Toxicol & Mil Pharm, Hradec Kralove, Czech Republic
关键词
PARAOXON-INHIBITED ACETYLCHOLINESTERASE; BISPYRIDINIUM COMPOUNDS BEARING; RAT-BRAIN ACETYLCHOLINESTERASE; NERVE AGENT; ORGANOPHOSPHATE INTOXICATION; CHOLINESTERASE REACTIVATORS; OXIME REACTIVATION; TABUN; LINKER; SERIES;
D O I
10.1039/c6ra16499d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Acetylcholinesterase (AChE) reactivators (oximes) are generally used as treatment in cases of nerve agent poisoning. There is no single oxime applicable in every case of nerve agent intoxication. Based on this fact, novel candidates with broader efficacy are still being sought. In this study, tetroxime a bisquaternary compound bearing four oxime groups, was evaluated for its potency to reactivate rat brain AChE inhibited by selected nerve agents (tabun, sarin, cyclosarin and VX agent). Despite the fact that this oxime contains four oxime groups that could be plausibly responsible for reactivation, it did not achieve broader reactivation activity. Satisfactory results were obtained only in the case of VX agent-inhibited AChE. In the cases of sarin-and cyclosarin-inhibited AChE, acceptable results were reached at higher oxime concentration only. Tetroxime was unable to reactivate tabun-inhibited AChE. However, compared with the gold standard pralidoxime, this oxime achieved more promising results.
引用
收藏
页码:7041 / 7045
页数:5
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