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新型双吡啶肟作为二异丙基氟磷酸酯抑制的乙酰胆碱酯酶复活剂的合成与评价

Synthesis and evaluation of novel bis-pyridinium oximes as reactivators of DFP-inhibited acetylcholinesterase.

作者信息

Acharya Jyotiranjan, Gupta Arvind Kumar, Dubey Devendra Kumar, Raza Syed Kalbey

机构信息

Process Technology Development Division, Defence Research and Development Establishment, Jhansi Road, Gwalior, Madhya Pradesh 474002, India.

出版信息

Eur J Med Chem. 2009 Mar;44(3):1335-40. doi: 10.1016/j.ejmech.2008.02.029. Epub 2008 Mar 7.

Abstract

A series of novel bis-pyridinium oximes connected by bis-methoxymethyl benzene, 1,4-bis-methoxymethyl (cis)-but-2-ene and 1,4-bis-methoxymethyl but-2-yne linkers were synthesized and their in vitro reactivation efficacy was evaluated against diisopropyl phosphorofluoridate (DFP) inhibited acetylcholinesterase (AChE) and compared with the established antidote 2-PAM and obidoxime. However, the best reactivation was observed with the standard oxime 2-PAM. The reactivation efficacy of 1,3-dimethoxymethyl benzene bis-[4,4'-(hydroxyiminomethyl) pyridinium] dichloride (3d) and 1,4-dimethoxy but-2-ene bis-[4,4'-(hydroxyiminomethyl) pyridinium] dichloride (3g) was comparable with that of obidoxime, another standard antidote.

摘要

合成了一系列通过双甲氧基甲基苯、1,4 - 双甲氧基甲基(顺式)- 丁 - 2 - 烯和1,4 - 双甲氧基甲基丁 - 2 - 炔连接基相连的新型双吡啶肟,并评估了它们对二异丙基氟磷酸酯(DFP)抑制的乙酰胆碱酯酶(AChE)的体外复活效力,并与已确立的解毒剂2 - PAM和氯解磷定进行了比较。然而,标准肟2 - PAM表现出最佳的复活效果。1,3 - 二甲氧基甲基苯双 - [4,4' - (羟基亚氨基甲基)吡啶鎓]二氯化物(3d)和1,4 - 二甲氧基丁 - 2 - 烯双 - [4,4' - (羟基亚氨基甲基)吡啶鎓]二氯化物(3g)的复活效力与另一种标准解毒剂氯解磷定相当。

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