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来自钩吻的甾体、生物碱和香豆素。

Steroids, alkaloids, and coumarins from Gelsemium sempervirens.

作者信息

Zhang Zhizhen, Wang Ping, Yuan Wei, Li Shiyou

机构信息

National Center for Pharmaceutical Crops, Arthur Temple College of Forestry and Agriculture, Stephen F. Austin State University, Nacogdoches, Texas, USA.

出版信息

Planta Med. 2008 Dec;74(15):1818-22. doi: 10.1055/s-0028-1088327. Epub 2008 Nov 17.

Abstract

The 95 % ethanol extract of Gelsemium sempervirens showed inhibitory activity against human DNA topoisomerase I (Topo I). Phytochemical investigations of this active extract resulted in the isolation and identification of three new steroids ( 1 - 3), together with eight known compounds 12 beta-hydroxy-5 alpha-pregn-16-ene-3,20-dione ( 4), gelsemine ( 5), sempervirine ( 6), scopoletin ( 7), 7- O- beta- D-glucopyranosylscopoletin ( 8), 7- O- beta- D-apiofuranosyl-(1-->6)- beta- D-glucopyranosylscopoletin ( 9), uvaol ( 10), and 2-(4-hydroxyphenyl)ethyl heptadecanoate ( 11). The structures of the new steroids were determined by extensive NMR and HR-ESI-MS analyses as 21-hydroxy-5 alpha-pregn-16-ene-3,20-dione ( 1), 3-oxoandrosta-16-ene-17-carboxylic acid ( 2), and 3-oxoandrosta-4,16-diene-17-carboxylic acid ( 3). This study suggests that sempervirine ( 6) intercalates to DNA and also inhibits Topo I through modulating the enzyme activity with an IC (50) of 54.5 +/- 15.9 muM.

摘要

钩吻的95%乙醇提取物对人DNA拓扑异构酶I(Topo I)显示出抑制活性。对该活性提取物进行植物化学研究,分离并鉴定出三种新的甾体化合物(1 - 3),以及八种已知化合物,分别为12β-羟基-5α-孕甾-16-烯-3,20-二酮(4)、钩吻碱(5)、钩吻素甲(6)、东莨菪素(7)、7 - O - β - D - 吡喃葡萄糖基东莨菪素(8)、7 - O - β - D - 芹菜糖基 -(1→6)- β - D - 吡喃葡萄糖基东莨菪素(9)、羽扇豆醇(10)和2 -(4 - 羟基苯基)乙基十七烷酸酯(11)。通过广泛的核磁共振(NMR)和高分辨电喷雾电离质谱(HR - ESI - MS)分析确定了新甾体化合物的结构,分别为21 - 羟基 - 5α - 孕甾 - 16 - 烯 - 3,20 - 二酮(1)、3 - 氧代雄甾 - 16 - 烯 - 17 - 羧酸(2)和和3 - 氧代雄甾 - 4,16 - 二烯 - 17 - 羧酸(3)。该研究表明,钩吻素甲(6)可插入DNA,并通过调节酶活性抑制Topo I,其半数抑制浓度(IC50)为54.5±15.9μM。

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