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首页> 外文期刊>Bulletin of the Korean Chemical Society >In vitro Screening of Oxime Reactivators on the Model of Paraoxon-inhibited Acetylcholinesterase-SAR Study
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In vitro Screening of Oxime Reactivators on the Model of Paraoxon-inhibited Acetylcholinesterase-SAR Study

机译:对氧磷抑制的乙酰胆碱酯酶-SAR研究模型中肟活化剂的体外筛选

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Acetylcholinesterase reactivators are crucial antidotes for the treatment of organophosphate intoxication. Standard in vitro test was chosen using a rat brain homogenate as the source of AChE. Screening of reactivation potency was performed with two concentration of reactivator (1000 μM and 10 μM). Results were compared to established reactivators pralidoxime, methoxime, HI-6, trimedoxime and obidoxime. More than 30 novel reactivators performed equal or better reactivation ability of POX-inhibited AChE compared to currently used reactivators. The structure-activity relationship for reactivators of paraoxon-inhibited AChE was developed.
机译:乙酰胆碱酯酶激活剂是治疗有机磷酸中毒的关键解毒剂。使用大鼠脑匀浆作为AChE的来源选择标准体外测试。用两种浓度的活化剂(1000μM和10μM)进行活化活性的筛选。将结果与确定的再活化剂普利昔肟,甲氧肟,HI-6,三甲肟和obidoxime进行比较。与当前使用的活化剂相比,超过30种新型活化剂具有与POX抑制的AChE相同或更好的活化能力。建立了对氧磷抑制的乙酰胆碱酯酶活化剂的构效关系。

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