Twelve different HI-6 salts and their potency to reactivate cyclosarin inhibited AChE in vitro

被引:12
|
作者
Kuca, Kamil [1 ]
Musilek, Kamil
Stodulka, Petr
Marek, Jan
Hanusova, Petra
Jun, Daniel
Hrabinova, Martina
Kassa, Jiri
Dolezal, Bohuslav
机构
[1] Univ Def Trebesska, Fac Mil Hlth Sci, Dept Toxicol, Hradec Kralove 50001, Czech Republic
[2] Univ Def Trebesska, Fac Mil Hlth Sci, Ctr Adv Studies, Hradec Kralove 50001, Czech Republic
[3] Charles Univ Prague, Fac Pharm, Fac Mil Hlth Sci, Dept Pharmaceut Chem, CS-50165 Hradec Kralove, Czech Republic
[4] Vakos XT as, Prague, Czech Republic
关键词
HI-6; reactivator; acetylcholinesterase; cyclosarine; nerve agent; salt; ion exchange; antidote; oxime; quaternary nitrogen;
D O I
10.2174/157018007781788462
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
As it is generally known, different anions of pharmaceutical preparations are generally developed to achieve better pharmacological effect through their adsorption phase. In this article, reactivation potency of twelve salts (sulfate, chloride, acetate, bromide, phosphate, mesylate, tartarate, iodide, malonate, salicylate, maleinate, tosylate) of bisquaternary acetylcholinesterase reactivator HI-6 was tested to elucidate that chemically different anions have no effect on the reactivation of nerve agent-inhibited acetylcholinesterase. For this purpose, cyclosarin was taken as the appropriate member of the nerve agent family. It was found that the use of different salts has no effect on the reactivation potency.
引用
收藏
页码:510 / 512
页数:3
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