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首页> 外文期刊>Bioorganic and Medicinal Chemistry >Monooxime reactivators of acetylcholinesterase with (E)-but-2-ene linker—Preparation and reactivation of tabun-and paraoxon-inhibited acetylcholinesterase
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Monooxime reactivators of acetylcholinesterase with (E)-but-2-ene linker—Preparation and reactivation of tabun-and paraoxon-inhibited acetylcholinesterase

机译:具有(E)-丁-2-烯连接基的乙酰胆碱酯酶的单肟激活物—塔宾和对氧磷抑制的乙酰胆碱酯酶的制备和激活

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摘要

Acetylcholinesterase reactivators are crucial antidotes for the treatment of organophosphate intoxication. Fifteen new monooxime reactivators of acetylcholinesterase with a (E)-but-2-ene linker were developed in an effort to extend the properties of K-oxime (E)-1-(4-carbamoylpyridinium)-4-(4-hydroxyiminomethylpyridinium)-but-2-ene dibromide (K203). The known reactivators (pralidoxime, HI-6, obidoxime, K075, K203) and the new compounds were tested in vitro on a model of tabun- and paraoxon-inhibited AChE. Monooxime reactivators were not able to exceed the best known compounds for tabun poisoning, but some of them did show reactivation comparable with known compounds for paraoxon poisoning. However, extensive differences were found by a SAR study for various substitutions on the non-oxime part of the reactivator molecule.
机译:乙酰胆碱酯酶活化剂是治疗有机磷酸中毒的关键解毒剂。为了扩展K-肟(E)-1-(4-氨基甲酰基吡啶)-4-(4-羟基亚氨基甲基吡啶)的性质,开发了15种带有(E)-丁-2-烯连接基的乙酰胆碱酯酶单肟活化剂。 -丁-2-烯二溴化物(K203)。已知的活化剂(普利昔肟,HI-6,obidoxime,K075,K203)和新化合物在受tabun和paraoxon抑制的AChE模型上进行了体外测试。单肟再活化剂不能超过已知的塔宾中毒化合物,但是其中一些确实表现出与已知的对氧磷中毒相当的化合物。但是,通过SAR研究发现,活化剂分子非肟部分的各种取代存在很大差异。

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