Stephtetrandrine A-D, bisbenzylisoquinoline alkaloids from Stephania tetrandra

被引:4
|
作者
Yang, Li-Jun [1 ,2 ]
Yang, Zhong-Duo [1 ]
Li, Zhi-Jie [1 ]
Yang, Shu-Hong [1 ]
Shu, Zong-Mei [1 ]
机构
[1] Lanzhou Univ Technol, Sch Life Sci & Engn, Lanzhou, Gansu, Peoples R China
[2] Univ Technol, Prov Educ Key Lab Screening Evaluat & Adv Proc Tr, Sch Life Sci & Engn, Lanzhou, Gansu, Peoples R China
基金
中国国家自然科学基金;
关键词
Stephania tetrandra; Menispermaceae; structure elucidation; bisbenzylisoquinoline alkaloids; enzyme inhibition; Stephtetrandrine; TUMOR INHIBITORS; FANGCHINOLINE; NEFERINE; ARREST; CELLS;
D O I
10.1080/14786419.2021.1961135
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Four undescribed bisbenzylisoquinoline alkaloids, designated as Stephtetrandrine A-D, were isolated from the roots of Stephania tetrandra. Their structures were elucidated by IR, HRESIMS, ECD spectra, 1 D and 2 D NMR spectra and comparison with the literature data. Additional five known compounds (limacine, tetrandrine, N-trans-Feruloyltyramine, 2 '-N-chloromethyltetrandrine, 2,2'-N-N-dichloromethyltetrandrine) were also isolated. N-trans-Feruloyltyramine was isolated from Stephania tetrandra for the first time. The isolated compounds were tested for monoamine oxidase, acetylcholinesterase, phosphoinositide 3-kinase alpha and human hepatoma cell HepG2 inhibitory activities. Stephtetrandrine C showed obvious inhibitory effect on human hepatoma HepG2, with IC50 value of 16.2 mu M. Limacine and 2 '-N-chloromethyltetrandrine showed moderate monoamine oxidase inhibitory effect with the IC50 values of 37.7 and 29.2 mu M, respectively.
引用
收藏
页码:204 / 215
页数:12
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