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抗肿瘤药,177. 叶下珠素6的分离与结构

Antineoplastic agents, 177. Isolation and structure of phyllanthostatin 6.

作者信息

Pettit G R, Schaufelberger D E, Nieman R A, Dufresne C, Saenz-Renauld J A

机构信息

Cancer Research Institute, Arizona State University, Tempe 85287-1604.

出版信息

J Nat Prod. 1990 Nov-Dec;53(6):1406-13. doi: 10.1021/np50072a002.

Abstract

The isolation and structural elucidation of a new Phyllanthus glycoside, phyllanthostatin 6 [7], was summarized. Phyllanthostatin 6 [7] was isolated from the roots of Phyllanthus acuminatus (Euphorbiaceae) and was found to inhibit (ED50 = 0.35 micrograms/ml) growth of the murine P-388 lymphocytic leukemia cell line. Two other new constituents were shown to be didesacetylphyllanthostatin 3 [9] and descinnamoylphyllanthocindiol [10]. Structure determinations were achieved employing hrfabms and 2D-nmr spectroscopy. Application of an hplc separation technique to the Phyllanthus glycosides and development of a new isolation procedure for the major antineoplastic constituent, phyllanthoside [1], are also described.

摘要

总结了一种新的叶下珠苷——叶下珠素6[7]的分离和结构解析。叶下珠素6[7]从尖叶下珠(大戟科)的根中分离得到,发现其能抑制(半数有效剂量=0.35微克/毫升)小鼠P-388淋巴细胞白血病细胞系的生长。另外两种新成分被证明是双去乙酰叶下珠素3[9]和去肉桂酰叶下珠二醇[10]。采用高分辨快原子轰击质谱和二维核磁共振光谱完成了结构测定。还描述了高效液相色谱分离技术在叶下珠苷中的应用以及主要抗肿瘤成分叶下珠苷[1]的新分离方法的开发。

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