牛膝中的蜕皮甾醇和三萜糖苷及其抑制 NO 生成的活性

Hoàng Thi Ngoc Lan, Nguyen Thi Ngoc Mai, Bui Thi Thao Anh, Duong Thi Dung, Bui Huu Tai, Phan Van Kiem
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摘要

通过对牛膝气生部分甲醇提取物进行植物化学研究,分离出了六种化合物,包括五种蜕皮甾醇,即makisterone A (1)、achyranthesterone A (2)、24(28)-dehydromakisterone A (3)、podecdysone C (4)、20-hydroxyecdysone (5)和3-O-α-L-rhamopyranosyl、24(28)-dehydromakisterone A (3)、podecdysone C (4)、20-hydroxyecdysone (5) 和 3-O-α-L-rhamnopyranosyl-(1→3)-β-D-glucuronopyranosyl-oleanolic acid 28-O-β-D-glucopyranosyl ester (6)。化合物 1-5 最早是从 A. aspera 中分离出来的。通过一维和一维核磁共振光谱与文献发表的数据进行对比,确定了它们的化学结构。与阳性对照化合物 L-NMMA 的 32.24 µM 相比,这五种蜕皮甾醇在 LPS 激活的 RAW264.7 细胞中明显表现出抑制 NO 生成的作用,IC50 值介于 27.21 至 40.47 µM 之间。
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Ecdysterols and triterpene glycoside from Achyranthes aspera L. and their NO production inhibitory activity
Phytochemical study on the methanolic extract of the aerial parts of Achyranthes aspera led to the isolation of six compounds including five ecdysterols, makisterone A (1), achyranthesterone A (2), 24(28)-dehydromakisterone A (3), podecdysone C (4), 20-hydroxyecdysone (5), and 3-O-α-L-rhamnopyranosyl-(1→3)-β-D-glucuronopyranosyl-oleanolic acid 28-O-β-D-glucopyranosyl ester (6). Compounds 1-5 were first isolated from A. aspera. Their chemical structures were identified by 1D and 1D NMR spectra in comparison with the published data in literature. Al five ecdysterol significantly showed NO production inhibition effects in LPS-activated RAW264.7 cells with the IC50 values ranging from 27.21 to 40.47 µM compared to that of positive control compound, L-NMMA, 32.24 µM.
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