Iguchi Tomoki, Uchida Yuka, Takano Shingo, Yokosuka Akihito, Mimaki Yoshihiro
Department of Medicinal Pharmacognosy, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences.
Chem Pharm Bull (Tokyo). 2020;68(3):273-287. doi: 10.1248/cpb.c19-01037.
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.
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。