Synthesis and in vitro screening of N-phenacylpyridinium oximes as reactivators of organophosphorus (OP)-inhibited electric eel acetylcholinesterase (AChE)

被引:0
作者
Valiveti, Aditya Kapil [1 ]
Acharya, Jyotiranjan [1 ]
Pratap, Ajay [1 ]
Halve, Anand K. [2 ]
Kaushik, Mahabir Parshad [1 ]
机构
[1] Def Res & Dev Estab, Proc Technol Dev Div, Gwalior 474002, India
[2] Jiwaji Univ, Sch Studies Chem, Gwalior 474011, India
关键词
Pyridinium oximes; Reactivators; 2-PAM; Obidoxime; Acetylcholinesterase; Phenacyl; Sarin; MONOQUATERNARY PYRIDINIUM OXIMES; RECOMBINANT HUMAN ACETYLCHOLINESTERASE; NERVE AGENTS; POTENCY; CHOLINESTERASES; ANTIDOTES; TOXICITY; EFFICACY;
D O I
10.1007/s00044-015-1384-y
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pyridinium oxime-based drugs are generally used in the treatment of acute organophosphorus (OP) nerve agent poisoning. In this regard, a series of mono-pyridinium oximes bearing substituted phenacyl moieties as side chain were synthesized and screened for their in vitro reactivation efficacies against electric eel acetylcholinesterase (AChE) inhibited by OP inhibitors such as DFP, sarin and VX. The results of the in vitro reactivation data of the synthesized compounds were compared to standard antidotes 2-PAM and obidoxime. Among the synthesized compounds, 1a, 2a, 7a, 8a, 11a, 12a, 13a, 14a and 16a have shown better reactivation efficacy than 2-PAM and obidoxime against VX-inhibited AChE. Oximes 8a, 8b, 11a and 12a were at par with obidoxime in the reactivation of sarin-inhibited AChE. The pKa values for all the oximes were determined and correlated with their observed reactivation potential.
引用
收藏
页码:3353 / 3371
页数:19
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