潘锡平, 秦永平, 陈若芸, 于德泉. 光叶紫玉盘多氧取代环己烯类成分研究J. 药学学报, 1998, 33(4): 275-281.
引用本文: 潘锡平, 秦永平, 陈若芸, 于德泉. 光叶紫玉盘多氧取代环己烯类成分研究J. 药学学报, 1998, 33(4): 275-281.
Pan Xiping, Qin Yongping, Chen Ruoyun , Yu Dequan, . STUDY ON THE POLYOXYGENATED CYCLOHEXENES FROM UVARIA BONIANAJ. Acta Pharmaceutica Sinica, 1998, 33(4): 275-281.
Citation: Pan Xiping, Qin Yongping, Chen Ruoyun , Yu Dequan, . STUDY ON THE POLYOXYGENATED CYCLOHEXENES FROM UVARIA BONIANAJ. Acta Pharmaceutica Sinica, 1998, 33(4): 275-281.

光叶紫玉盘多氧取代环己烯类成分研究

STUDY ON THE POLYOXYGENATED CYCLOHEXENES FROM UVARIA BONIANA

  • 摘要: 从番荔枝科紫玉盘属植物光叶紫玉盘(Uvaria boniana Finet)地上茎EtOH提取物中分离出7种新的多氧取代环己烯类化合物,用波谱分析和Mosher酯制备等方法确定了全部化学结构及其绝对构型,分别命名为光叶紫玉盘醇A~G(uvaribonolA~G,1~7)。体外抗肿瘤筛选表明,这些天然化合物均无活性,但部分半合成衍生物活性明显,其中尤以光叶紫玉盘醇B(2)的氧化物(2a)最为显著,抑制KB、Bel7402和A2780细胞的IC50值均小于1μg·ml-1,抑制HCT-8的IC50则小于0.1μg·ml-1

     

    Abstract: Seven new polyoxygenated cyclohexenes,named uvaribonol A~G (1~7) have been isolated from the ethanol extract of the stems of Uvaria boniana Finet. (Annonaceae), and their structures, including the absolute configuration, were determined by spectral and chemical methods. In vitro cytotoxicity test against several human tumor cell lines indicated that all of the new natural compounds are inactive, but some of the derivatives showed obvious activities. Compound 2a is the most active, exhibiting significant cytotoxicities against KB and Bel7402 cells with IC50<1 μg·ml-1, and against HCT-8 cell with IC50 <0.1 μg·ml-1.

     

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