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黑藜芦全草中的甾体成分及其体外细胞毒性。

Steroidal constituents in the whole plants of Helleborus niger and their cytotoxic activity in vitro.

机构信息

Department of Medicinal Pharmacognosy, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo, 192-0392, Japan.

Department of Medicinal Pharmacognosy, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, 1432-1 Horinouchi, Hachioji, Tokyo, 192-0392, Japan.

出版信息

Phytochemistry. 2025 Jan;229:114272. doi: 10.1016/j.phytochem.2024.114272. Epub 2024 Sep 12.

Abstract

Phytochemical investigation of the whole plants of Helleborus niger L. (Ranunculaceae) resulted in the isolation of five undescribed compounds, including one bufadienolide (1), two bufadienolide rhamnosides (2 and 3), and two ecdysteroids (12 and 13), along with eight known compounds (4-11). The chemical structures of 1-3, 12, and 13 were determined by spectroscopic studies, including 2D NMR, and chromatographic and spectroscopic analyses of the hydrolyzed products. Compounds 1-13 were evaluated for their cytotoxic activity against HL-60 human leukemia cells, A549 human lung adenocarcinoma cells, SBC-3 human small-cell lung cancer cells, and TIG-3 human normal diploid lung cells. Compounds 1-12 showed cytotoxic activity against HL-60, A549, and SBC-3 cells, with IC values ranging from 0.0016 to 6.1 μM. Bufadienolide rhamnoside 2 exhibited potent cell proliferation inhibitory activity against SBC-3 cells after 24-48 h of treatment and apoptosis-inducing activity in SBC-3 cells via an intrinsic pathway after 72 h of treatment. The JFCR39 panel screening of 2 suggests that the molecular target of 2 is Na,K-ATPase.

摘要

黑藜芦(毛茛科)全植物的植物化学研究导致分离出五种未描述的化合物,包括一种蟾蜍二烯内酯(1)、两种蟾蜍二烯内酯鼠李糖苷(2 和 3)和两种蜕皮甾酮(12 和 13),以及八种已知化合物(4-11)。通过光谱研究,包括二维 NMR 以及水解产物的色谱和光谱分析,确定了 1-3、12 和 13 的化学结构。对化合物 1-13 进行了细胞毒性活性评价,针对 HL-60 人白血病细胞、A549 人肺腺癌细胞、SBC-3 人小细胞肺癌细胞和 TIG-3 人正常二倍体细胞。化合物 1-12 对 HL-60、A549 和 SBC-3 细胞具有细胞毒性活性,IC 值范围为 0.0016 至 6.1 μM。在治疗 24-48 小时后,鼠李糖苷 2 对 SBC-3 细胞表现出强烈的细胞增殖抑制活性,并且在治疗 72 小时后通过内在途径诱导 SBC-3 细胞凋亡。2 的 JFCR39 小组筛选表明,2 的分子靶标是 Na,K-ATPase。

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