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[Relation between chemical structure and cholinesterase-reactivating effect in a series of new asymmetric pyridinium salts. I. Derivatives of 4-hydroxyiminomethylpyridine].

作者信息

Dirks E, Scherer A, Schmidt M, Zimmer G

出版信息

Arzneimittelforschung. 1970 Jan;20(1):55-62.

PMID:5467448
Abstract
摘要

相似文献

1
[Relation between chemical structure and cholinesterase-reactivating effect in a series of new asymmetric pyridinium salts. I. Derivatives of 4-hydroxyiminomethylpyridine].[一系列新型不对称吡啶鎓盐的化学结构与胆碱酯酶复活作用的关系。I. 4-羟基亚胺甲基吡啶的衍生物]
Arzneimittelforschung. 1970 Jan;20(1):55-62.
2
[Relations between chemical structure and cholinesterase-reactivating effect in a series of new asymmetric pyridinium salts. II. 2-hydroximino-methylpyridine derivates].[一系列新型不对称吡啶鎓盐的化学结构与胆碱酯酶复活作用之间的关系。II. 2-羟基亚氨基甲基吡啶衍生物]
Arzneimittelforschung. 1970 Feb;20(2):197-200.
3
Protective action of series of new mono-pyridinium salts and their effect on "aging" of acetylcholine esterase inhibited by fluostigmine.一系列新型单吡啶鎓盐的保护作用及其对被毒扁豆碱抑制的乙酰胆碱酯酶“老化”的影响。
Pol J Pharmacol Pharm. 1977 Nov-Dec;29(6):603-7.
4
Quaternary salts of 4,3' and 4,4' bis-pyridinium monooximes: synthesis and biological activity.
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Protective effects of a series of new pyridinium derivatives against inhibition of acetylcholinesterase by fluostigmine.一系列新型吡啶鎓衍生物对氟斯的明抑制乙酰胆碱酯酶的保护作用。
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Synthesis and biological activity of pyridinium-type acetylcholinesterase inhibitors.吡啶型乙酰胆碱酯酶抑制剂的合成及生物活性
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Synthesis and Evaluation of Chroman-4-One Linked to N-Benzyl Pyridinium Derivatives as New Acetylcholinesterase Inhibitors.作为新型乙酰胆碱酯酶抑制剂的与N-苄基吡啶鎓衍生物相连的色满-4-酮的合成与评价
Arch Pharm (Weinheim). 2015 Sep;348(9):643-9. doi: 10.1002/ardp.201500149. Epub 2015 Jul 20.
8
Proceedings: Effects of pinacolyl-pyridinium derivatives on structure-bound acetylcholinesterase (E.C.3.1.1.7.) in vitro.论文集:频哪基吡啶衍生物对体外结构结合型乙酰胆碱酯酶(E.C.3.1.1.7.)的影响
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9
Synthesis of the novel series of bispyridinium compounds bearing (E)-but-2-ene linker and evaluation of their reactivation activity against chlorpyrifos-inhibited acetylcholinesterase.含(E)-丁-2-烯连接基的新型双吡啶鎓化合物系列的合成及其对毒死蜱抑制的乙酰胆碱酯酶的复活活性评价。
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Monoquaternary pyridinium salts with modified side chain-synthesis and evaluation on model of tabun- and paraoxon-inhibited acetylcholinesterase.具有修饰侧链的单季铵吡啶盐的合成及其对塔崩和对氧磷抑制乙酰胆碱酯酶模型的评价
Bioorg Med Chem. 2008 Sep 1;16(17):8218-23. doi: 10.1016/j.bmc.2008.07.036. Epub 2008 Jul 20.

引用本文的文献

1
Reactivating and protective effects of pyridinium compounds in human erythrocyte acetylcholinesterase inhibition by organophosphates in vitro.吡啶鎓化合物对有机磷酸酯体外抑制人红细胞乙酰胆碱酯酶的复活及保护作用
Arch Toxicol. 1980 May;45(1):21-7. doi: 10.1007/BF00303291.
2
Characterization of cholinesterases in various tissues of guinea pig with respect to their reactivation by obidoxime after inactivation by diisopropylfluorophosphate.用双异丙基氟磷酸酯使豚鼠各组织中的胆碱酯酶失活后,观察其被氯解磷定重新激活的情况,对各组织中的胆碱酯酶进行表征。
Arch Toxikol. 1972;29(3):235-45. doi: 10.1007/BF00315601.
3
Reversible and irreversible inhibition of rat brain muscarinic receptors is related to different substitutions on bisquaternary pyridinium oximes.
Arch Toxicol. 1985 Oct;58(1):37-9. doi: 10.1007/BF00292614.