冯卫生, 郭孟焕, 殷艺阁, 曹彦刚, 杨翠兰, 王洋洋, 齐曼, 张艳丽, 任英杰, 刘晏灵, 郑晓珂. 零余子中一个新的吲哚类生物碱J. 药学学报, 2018,53(7): 1131-1133. doi: 10.16438/j.0513-4870.2018-0400
引用本文: 冯卫生, 郭孟焕, 殷艺阁, 曹彦刚, 杨翠兰, 王洋洋, 齐曼, 张艳丽, 任英杰, 刘晏灵, 郑晓珂. 零余子中一个新的吲哚类生物碱J. 药学学报, 2018,53(7): 1131-1133. doi: 10.16438/j.0513-4870.2018-0400
FENG Wei-sheng, GUO Meng-huan, YIN Yi-ge, CAO Yan-gang, YANG Cui-lan, WANG Yang-yang, QI Man, ZHANG Yan-li, REN Ying-jie, LIU Yan-ling, ZHENG Xiao-ke. A new indole alkaloid from bulbils of Dioscorea opposite Thunb.J. Acta Pharmaceutica Sinica, 2018,53(7): 1131-1133. doi: 10.16438/j.0513-4870.2018-0400
Citation: FENG Wei-sheng, GUO Meng-huan, YIN Yi-ge, CAO Yan-gang, YANG Cui-lan, WANG Yang-yang, QI Man, ZHANG Yan-li, REN Ying-jie, LIU Yan-ling, ZHENG Xiao-ke. A new indole alkaloid from bulbils of Dioscorea opposite Thunb.J. Acta Pharmaceutica Sinica, 2018,53(7): 1131-1133. doi: 10.16438/j.0513-4870.2018-0400

零余子中一个新的吲哚类生物碱

A new indole alkaloid from bulbils of Dioscorea opposite Thunb.

  • 摘要: 采用柱色谱技术分离纯化研究零余子(bulbils of Dioscorea opposite Thunb.)中的化学成分。通过理化性质和波谱数据鉴定了4个吲哚类生物碱:零余子碱(3,4-dihydro-6-hydroxy-4-methyl-6H-pyrido6,5-bindol-5(1H)-one)(1)、anoectochine (2)、ginsenine (3)和吲哚乳酸酯(4)。其中化合物1为新化合物,命名为:零余子碱,化合物2~4均为首次从该植物中得到。通过MTT法评价化合物的细胞毒活性,这4个化合物对人肝瘤细胞HepG2和乳腺癌细胞MDA-231的IC50值均大于100μmol·L-1,均未表现出明显的细胞毒活性。

     

    Abstract: This study was designed to study the chemical constituents from bulbil of Dioscorea opposite Thunb.. Four compounds were isolated by silica gel column chromatography. On the basis of physic-chemical characters and spectroscopic data analysis, these compounds were identified as lyzalkaloid (3,4-dihydro-6-hydroxy-4-methyl-6H-pyrido6,5-bindol-5(1H)-one) (1), anoectochine (2), ginsenine (3), and 2-hydroxy-3-(1H-indol-3-yl) propanoic acid methyl ester (4). Compound 1 is a new indole alkaloid, named as lyzalkaloid. Compounds 2-4 were isolated from this plant for the first time. The cytotoxic activities were assessed by MTT assay. All compounds exhibited the cytotoxic activity against HepG2 and MDA-231 with IC50 values of over 100 μmol·L-1, respectively. All compounds show no significant cytotoxic activities against HepG2, MDA-231 cancer cell.

     

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