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来自臭嚏根草全株的新型甾体糖苷。

Novel Steroidal Glycosides from the Whole Plants of Helleborus foetidus.

作者信息

Iguchi Tomoki, Uchida Yuka, Takano Shingo, Yokosuka Akihito, Mimaki Yoshihiro

机构信息

Department of Medicinal Pharmacognosy, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences.

出版信息

Chem Pharm Bull (Tokyo). 2020;68(3):273-287. doi: 10.1248/cpb.c19-01037.

Abstract

Phytochemical analysis of the whole Helleborus foetidus plants identified 28 steroidal glycosides (1-28), including 20 novel spirostanol glycosides (1-20) and a novel furostanol glycoside (21). The structures of the newly identified compounds were elucidated by two-dimensional NMR spectroscopy and hydrolytic cleavage. Compounds 12, 13, and 15 were determined to be spirostanol trisdesmosides bearing sugar moieties at the C-1, -21, and -24 hydroxy groups of the aglycone unit. The isolated compounds were subsequently evaluated for cytotoxic activity against HL-60 human promyelocytic leukemia cells and A549 human lung carcinoma cells. In particular, 7 showed cytotoxic activity against the HL-60 and A549 cells, with IC values of 5.9 and 6.6 µM, respectively, whereas 19 was selectively cytotoxic to A549 cells with an IC value of 5.5 µM.

摘要

对臭嚏根草全株进行的植物化学分析鉴定出28种甾体苷(1 - 28),其中包括20种新型螺旋甾烷醇苷(1 - 20)和1种新型呋甾烷醇苷(21)。通过二维核磁共振光谱和水解裂解确定了新鉴定化合物的结构。化合物12、13和15被确定为在苷元单元的C - 1、- 21和- 24羟基上带有糖部分的螺旋甾烷醇三糖苷。随后评估了分离出的化合物对HL - 60人早幼粒细胞白血病细胞和A549人肺癌细胞的细胞毒性活性。特别是,化合物7对HL - 60和A549细胞显示出细胞毒性活性,IC值分别为5.9和6.6 μM,而化合物19对A549细胞具有选择性细胞毒性,IC值为5.5 μM。

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