A New Quinolizidine Alkaloid from Sophora flavescens

被引:20
|
作者
Wang Lei [1 ,2 ,3 ]
Wu Xing-De [3 ]
He Juan [3 ]
Li Gen-Tao [3 ]
Peng Li-Yan [3 ]
Li Yan [3 ]
Song Liu-Dong [1 ,2 ]
Zhao Qin-Shi [3 ]
机构
[1] Kunming Med Univ, Sch Pharmaceut Sci, Kunming 650500, Peoples R China
[2] Kunming Med Univ, Yunnan Key Lab Pharmacol Nat Prod, Kunming 650500, Peoples R China
[3] Chinese Acad Sci, Kunming Inst Bot, State Key Lab Phytochem & Plant Resources West Ch, Kunming 650201, Peoples R China
关键词
Sophora flavescens; Leguminosae; alkaloids; cytotoxicity; LUPIN ALKALOIDS;
D O I
10.1007/s10600-014-1104-8
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
We studied the alkaloid constituents and bioactivity of Sophora flavescens (Leguminosae). The constituents were isolated with silica gel column chromatography, semi-preparative HPLC, Sephadex LH-20, and MPLC packed with MCI gel, and their structures were elucidated on the basis of physical characteristics and spectral data. Compounds 1 and 5-8 were evaluated for their in vitro cytotoxicity against human tumor HL-60, SMMC-7721, A-549, MCF-7, and SW-480 cell lines. Ten alkaloids were obtained, and their structures were identified as 17 beta-hydroxysophoridine (1), matrine (2), sophocarpine (3), sophoridine (4), isomatrine (5), 7,11-dehydromatrine (6), mamanine (7), sophoranol (8), oxymatrine (9), and oxysophocarpine (10). Compound 1 is a new alkaloid, and compound 7 was isolated from the Sophora flavescens for the first time. None of the compounds were cytotoxic to five human cancer cell lines.
引用
收藏
页码:876 / 879
页数:4
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