Synthesis and anticholinesterase activity of thioesters of chlorofluoronitroacetic acid
作者:Yu. Ya. Ivanov、V. I. Uvarov、V. K. Brel'、I. V. Martynov
DOI:10.1007/bf00769645
日期:1988.5
esters of chlorofluoronitroacetic acid showed high activity as irreversible inhibitors of cholinesterase (CE) [2, 3]. With the aim of exploring new inhibitors among this class of compounds, we synthesized thioesters of chlorofluoronitroacetic acid O2NCFCICOSR (Ia, b), R = Et (la) and Bu (Ib). The present work gives the results of a study of their anticholinesterase activity. They were compared in effectiveness
最近发现,氯氟硝基乙酸酯作为胆碱酯酶 (CE) 的不可逆抑制剂显示出高活性 [2, 3]。为了在此类化合物中探索新的抑制剂,我们合成了氯氟硝基乙酸的硫酯 O2NCFCICOSR (Ia, b)、R = Et (la) 和 Bu (Ib)。目前的工作给出了其抗胆碱酯酶活性的研究结果。将它们与氧类似物、氯氟硝基乙酸的乙酯 (IIa) 和丁酯 (IIb) 的有效性进行了比较。