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来自卷丹的四种新甾体苷及其抗肿瘤活性。

Four new steroidal glycosides from Lilium lancifolium Thunb. and their antitumor activity.

作者信息

Zhou Jing, Zhao Xin-Meng, An Ren-Feng, Li Xiao-Rui, Wu Kai-Tian, Li Shu-Ming, Huang Xue-Feng

机构信息

Department of Natural Medicinal Chemistry, School of Traditional Chinese Pharmacy, China Pharmaceutical University, Nanjing 210009, China.

School of Chemical Engineering, Hebei University of Technology, Tianjin 300130, China; Tasly Academy, Tasly Holding Group Co Ltd., Tianjin 300410, China.

出版信息

Fitoterapia. 2024 Mar;173:105808. doi: 10.1016/j.fitote.2023.105808. Epub 2023 Dec 31.

Abstract

Four new steroidal glycosides (1-4), including two steroidal saponins named lililancifoloside B and C (1-2), one pregnane glycoside named lililancifoloside D (3), and one C22-steroidal lactone glycoside named lililancifoloside E (4), together with five known ones (5-9), were isolated from the bulbs of Lilium lancifolium Thunb. By using spectroscopic analysis, including 1D, 2D NMR, and HR-ESI-MS, the structures of 1-4 were elucidated. All isolates were tested for their cytotoxic potential against the MCF-7, MDA-MB-231, HepG2, and A549 cell lines. Compound 6 distinguished out among them, IC values of 3.31, 5.23, 1.78, and 1.49 μM against the four cell lines, respectively. Other compounds such as compound 3, 5, and 9 have also shown specific cytotoxic activity. Next, studies showed that compound 6 might cause HepG2 cells to undergo a cell cycle arrest during the G2/M phase and apoptosis.

摘要

从卷丹的鳞茎中分离出4个新的甾体糖苷(1-4),包括2个甾体皂苷,分别命名为卷丹皂苷B和C(1-2),1个孕甾烷糖苷,命名为卷丹皂苷D(3),以及1个C22甾体内酯糖苷,命名为卷丹皂苷E(4),同时还分离出5个已知化合物(5-9)。通过1D、2D NMR和HR-ESI-MS等光谱分析方法阐明了1-4的结构。对所有分离物进行了针对MCF-7、MDA-MB-231、HepG2和A549细胞系的细胞毒性潜力测试。化合物6在其中表现突出,对这4种细胞系的IC值分别为3.31、5.23、1.78和1.49 μM。其他化合物如化合物3、5和9也表现出特定的细胞毒性活性。接下来的研究表明,化合物6可能导致HepG2细胞在G2/M期发生细胞周期阻滞并诱导凋亡。

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