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裸花紫珠中的环烯醚萜苷

Iridoid glycosides from Callicarpa nudiflora Hook.

作者信息

Feng Shi-Xiu, Yi Bo, Zhang Min, Xu Jing, Lin Hai, Xu Wen-Tong

机构信息

a Key Laboratory of South Subtropical Plant Diversity , Fairy Lake Botanical Garden, Shenzhen & Chinese Academy of Sciences , Shenzhen , China.

b Pharmacy Department of the 187th Hospital of People's Liberation Army , Haikou , China.

出版信息

Nat Prod Res. 2017 Jan;31(2):181-189. doi: 10.1080/14786419.2016.1224872. Epub 2016 Sep 21.

Abstract

Four new iridoid glycoside derivatives (1-4), along with ten known iridoid glycosides (5-14), were isolated from Callicarpa nudiflora Hook et Arn. The structure of the new iridoid glycosides was elucidated as 5″-methoxy-ampicoside (1), 6″-O-trans-caffeoylcatalpol (2), 6″-O-trans-feruloylcatalpol (3) and 3″-methoxy-agnucastoside C (4) on the basis of spectroscopic analysis. Compounds 1-11 were reported from this plant for the first time. The cytotoxic activity of the isolated compounds against human cervical carcinoma Hela cells and ovarian carcinoma HeyA8 cells was evaluated using the microculture tetrazolium assay. Compounds 4, 5, 8, 12 and 13 showed cytotoxic activity against the Hela cell line with IC values of 25.3, 48.1, 17.3, 38.3 and 28.2 μM, respectively. While only compound 8 showed cytotoxicity against the HeyA8 cell line, with an IC of 35.5 μM.

摘要

从裸花紫珠中分离得到4个新的环烯醚萜苷衍生物(1-4)以及10个已知的环烯醚萜苷(5-14)。通过光谱分析确定新环烯醚萜苷的结构分别为5″-甲氧基-氨苄糖苷(1)、6″-O-反式咖啡酰梓醇(2)、6″-O-反式阿魏酰梓醇(3)和3″-甲氧基-agnucastoside C(4)。化合物1-11首次从该植物中报道。采用微量培养四氮唑法评估分离得到的化合物对人宫颈癌Hela细胞和卵巢癌HeyA8细胞的细胞毒活性。化合物4、5、8、12和13对Hela细胞系表现出细胞毒活性,IC值分别为25.3、48.1、17.3、38.3和28.2 μM。而只有化合物8对HeyA8细胞系表现出细胞毒性,IC值为35.5 μM。

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