[从杉木中分离出一种新的头孢他辛型生物碱二聚体]。

Q3 Pharmacology, Toxicology and Pharmaceutics
Jia-Yang Ma, Jing Wang, Sha Chen, Chun-Lei Yuan, Jin-Yuan Yang, Da-Hong Li, Hui-Ming Hua
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引用次数: 0

摘要

采用十八烷基硅烷(ODS)、硅胶、Sephadex LH-20柱层析和半制备高效液相色谱(HPLC)等多种色谱技术对杉木头杉(Cephalotaxus lanceolata)的化学成分进行分离纯化。利用核磁共振(NMR)、质谱(MS)、紫外(UV)等光谱方法结合文献资料,鉴定了17个化合物。化合物1是一个新的生物碱二聚体,名叫cephalancetine e .已知化合物测定cephalancetine (2), 11-hydroxycephalotaxine (3), 4-hydroxycephalotaxine (4), cephalotaxine (5), epicephalotaxine (6), cephalotaxineβ-N-oxide (7), acetylcephalotaxine (8), cephalotine (9), cephalotine B (10), 11-hydroxycephalotaxine半缩酮(11),3-deoxy-3, 11-epoxy-cephalotaxine (12), cephalotaxinone (13), isocephalotaxinone (14), 2, 11-epoxy-1, 2-dihydro-8-oxo-cephalotaxine (15), cephalotaxamide (16),和drupacine(17)。化合物11、12、15为首次从该属植物中分离得到。测定了化合物1 ~ 17的生物活性。结果表明,化合物17对3种人类癌细胞(HepG-2、MCF-7和SH-SY5Y)具有较强的抑制活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[A new cephalotaxine-type alkaloid dimer from Cephalotaxus lanceolata].

The chemical constituents from Cephalotaxus lanceolata were isolated and purified by using multiple chromatographic techniques, including octadecylsilane(ODS), silica gel, Sephadex LH-20 column chromatography, and semi-preparative high-performance liquid chromatography(HPLC). A total of 17 compounds obtained were identified by using spectroscopic methods such as nuclear magnetic resonance(NMR), mass spectrometry(MS), and ultraviolet(UV) combined with literature data. Compound 1 was a new alkaloid dimer, named cephalancetine E. The known compounds were determined as cephalancetine A(2), 11-hydroxycephalotaxine(3), 4-hydroxycephalotaxine(4), cephalotaxine(5), epicephalotaxine(6), cephalotaxine β-N-oxide(7), acetylcephalotaxine(8), cephalotine A(9), cephalotine B(10), 11-hydroxycephalotaxine hemiketal(11), 3-deoxy-3,11-epoxy-cephalotaxine(12), cephalotaxinone(13), isocephalotaxinone(14), 2,11-epoxy-1,2-dihydro-8-oxo-cephalotaxine(15), cephalotaxamide(16), and drupacine(17), respectively. Compounds 11, 12, and 15 were isolated from the Cephalotaxus genus for the first time. The biological activity was tested for compounds 1-17. The results reveal that compound 17 displays potent inhibitory activities against three human cancer cell lines(HepG-2, MCF-7, and SH-SY5Y).

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来源期刊
Zhongguo Zhongyao Zazhi
Zhongguo Zhongyao Zazhi Pharmacology, Toxicology and Pharmaceutics-Pharmacology, Toxicology and Pharmaceutics (all)
CiteScore
1.50
自引率
0.00%
发文量
581
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