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从卷柏中分离出的穗花杉双黄酮衍生物及其细胞毒性活性。

Isolation and cytotoxic activity of selaginellin derivatives and biflavonoids from Selaginella tamariscina.

机构信息

College of Traditional Chinese Materia Medica, Shenyang Pharmaceutical University, Shenyang, P. R. China.

出版信息

Planta Med. 2012 Mar;78(4):390-2. doi: 10.1055/s-0031-1298175. Epub 2012 Jan 23.

Abstract

Five selaginellin derivatives, including two new selaginellins termed selaginellins M (1) and N (2), and three previously identified compounds, selaginellin (3), selaginellin A (4), and selaginellin C (5), were isolated from the Selaginella tamariscina (Beauv.) Spring plant. In addition, four known biflavonoids, namely neocryptomerin ( 6), hinokiflavone (7), pulvinatabiflavone (8), and 7''- O-methylamentoflavone (9), were also isolated. The structures of new compounds 1 and 2 were elucidated by spectroscopic analysis. The cytotoxic activity of compounds 1- 9 was evaluated against a small panel of human cancer cell lines, including U251 (human glioma cells), HeLa (human cervical carcinoma cells), and MCF-7 (human breast cancer cells). The two new selaginellins, selaginellins M (1) and N (2), showed medium activity against the human cancer cell lines.

摘要

从卷柏(Beauv.)Spring 植物中分离得到了 5 种卷柏素衍生物,包括 2 种新型卷柏素,即卷柏素 M(1)和 N(2),以及 3 种先前鉴定的化合物,即卷柏素(3)、卷柏素 A(4)和卷柏素 C(5)。此外,还分离得到了 4 种已知的双黄酮类化合物,即新隐黄素(6)、扁柏黄素(7)、大波斯菊黄素(8)和 7''-O-甲基amentoflavone(9)。新化合物 1 和 2 的结构通过光谱分析阐明。对化合物 1-9 对一组小型人类癌细胞系(包括 U251(人神经胶质瘤细胞)、HeLa(人宫颈癌细胞)和 MCF-7(人乳腺癌细胞))的细胞毒性活性进行了评估。两种新型的卷柏素,即卷柏素 M(1)和 N(2),对人癌细胞系显示出中等活性。

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