精选吲哚类化合物的合成和胆碱酯酶抑制活性。

IF 1.2 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY
Uroš Grošelj, Marija Gršič, Anže Meden, Damijan Knez, Marko Jukič, Jurij Svete, Stanislav Gobec
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引用次数: 0

摘要

本研究公开了 18 种以前未发表过的吲哚和色氨酸衍生化合物的合成和抗胆碱酯酶活性。这些富含 sp3 的化合物含有一个吲哚结构单元,对人丁酰胆碱酯酶(hBChE)具有选择性亚摩尔抑制作用。新合成化合物的结构通过 1H 和 13C NMR、红外光谱以及高分辨率质谱法得到了证实。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Synthesis and Cholinesterase Inhibitory Activity of Selected Indole-Based Compounds.

Synthesis and anticholinesterase activity of 18 previously unpublished indole- and tryptophan-derived compounds are disclosed. These sp3-rich compounds containing an indole structural unit exhibit selective submicromolar inhibition of human butyrylcholinesterase (hBChE). The structures of the newly synthesized compounds were confirmed by 1H and 13C NMR, IR spectroscopy, and high-resolution mass spectrometry.

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来源期刊
Acta Chimica Slovenica
Acta Chimica Slovenica 化学-化学综合
CiteScore
2.50
自引率
25.00%
发文量
80
审稿时长
1.0 months
期刊介绍: Is an international, peer-reviewed and Open Access journal. It provides a forum for the publication of original scientific research in all fields of chemistry and closely related areas. Reviews, feature, scientific and technical articles, and short communications are welcome.
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