化学
水解物
赫拉
呋喃
细胞毒性
立体化学
二维核磁共振波谱
戒指(化学)
IC50型
体外
生物化学
有机化学
水解
作者
Xiao-San Li,Juan Long,Mei‐Fang Chen,Qilin Wang,Xiao-Yan Liang,Jia-Chon Zheng,Rui Xing,Xuemei Yang,Yongmei Huang,Hui Luo
标识
DOI:10.1016/j.tetlet.2022.153812
摘要
Cynotofuranoside A-C (1–3), three previously undescribed C21-steroidal furanosides were isolated from the acid hydrolysate of Cynanchum otophyllum roots. Their structures were elucidated by extensive spectroscopic analysis including UV, IR, 1D and 2D NMR and HR-ESI-MS. Compounds 1–3 represented the first examples of 2,6-dideoxy-aldohexose in the form of furan ring attaching to 3β-OH of natural occurring C21-steroidal aglycones. The cytotoxicity of these compounds against human cancer MCF-7, HCT-116, HeLa, and HepG2 cells were evaluated. Compounds 1 and 3 showed moderate cytotoxic activities against HepG2 cancer cells with IC50 values of 43.15 and 34.36 μM, respectively.
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