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石蒜科水仙属不同结构类型生物碱及其生物活性。

Alkaloids from Narcissus poeticus cv. Pink Parasol of various structural types and their biological activity.

机构信息

ADINACO Research Group, Department of Pharmaceutical Botany and Ecology, Faculty of Pharmacy, Charles University, Heyrovského 1203, 500 05, Hradec Kralove, Czech Republic.

Department of Toxicoloxy and Military Pharmacy, Faculty of Military Health Sciences, University of Defence, Třebešská 1575, 500 05, Hradec Kralove, Czech Republic.

出版信息

Arch Pharm Res. 2018 Feb;41(2):208-218. doi: 10.1007/s12272-017-1000-4. Epub 2017 Dec 14.

Abstract

Fifteen Amaryllidaceae alkaloids (1-15) of various structural types were isolated by standard chromatographic methods from fresh bulbs of Narcissus poeticus cv. Pink Parasol. The chemical structures were elucidated by MS, and 1D and 2D NMR spectroscopic analyses, and by comparison with literature data. Narcipavline (5) and narcikachnine (6) are reported here for the first time. In their structure are combined two basic structural types of Amaryllidaceae alkaloids (galanthamine- and galanthindole-structural types), which represent a new structural type of these compounds. Alkaloids isolated in sufficient amounts were evaluated for their human erythrocytic acetylcholinesterase, and human serum butyrylcholinesterase (HuBuChE) inhibition activity using Ellman's method. Z-Gly-Pro-p-nitroanilide was used as substrate in the prolyl oligopeptidase (POP) assay. Untested alkaloids were also screened for their cytotoxic activity against a small panel of human cancer cells, which spanned cell lines from different tissue types. In parallel, MRC-5 human fibroblasts were employed to determine overall toxicity against noncancerous cells. Some compounds were evaluated for their antiprotozoal activity. The newly isolated alkaloid narcipavline (5) showed interesting HuBuChE inhibition activity (IC = 24.4 ± 1.2 µM), and norlycoramine (11) demonstrated promising POP inhibition (IC = 0.21 ± 0.01 mM).

摘要

从水仙诗歌品种的新鲜鳞茎中,通过标准色谱方法分离出 15 种具有不同结构类型的石蒜科生物碱(1-15)。通过 MS、1D 和 2D NMR 光谱分析以及与文献数据的比较,阐明了它们的化学结构。这里首次报道了水仙碱(5)和水仙卡宁(6)。它们的结构结合了石蒜科生物碱的两种基本结构类型(加兰他敏和加兰他因结构类型),代表了这些化合物的一种新结构类型。分离出足够量的生物碱,并用 Ellman 法评估它们对人红细胞乙酰胆碱酯酶和人血清丁酰胆碱酯酶(HuBuChE)的抑制活性。Z-Gly-Pro-p-硝基苯胺用作脯氨酰寡肽酶(POP)测定中的底物。未经测试的生物碱也针对一组小的人类癌细胞进行了细胞毒性筛选,这些细胞跨越了来自不同组织类型的细胞系。同时,使用 MRC-5 人成纤维细胞来确定对非癌细胞的整体毒性。一些化合物被评估了抗原生动物活性。新分离的生物碱水仙碱(5)显示出有趣的 HuBuChE 抑制活性(IC=24.4±1.2µM),而去甲藜芦碱(11)表现出有希望的 POP 抑制活性(IC=0.21±0.01mM)。

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