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白头翁皂苷A、D衍生物的合成、细胞毒性及溶血活性

Synthesis, cytotoxicity and haemolytic activity of Pulsatilla saponin A, D derivatives.

作者信息

Chen Zhong, Duan Huaqing, Wang Minglei, Han Li, Liu Yanli, Zhu Yongming, Yang Shilin

机构信息

College of Pharmaceutical Science, Soochow University, 199 Ren Ai Road, Suzhou 215123, China.

Zhang Zhongjing College of Chinese Medicine, Nanyang Institute of Technology, 80 Chang Jiang Road, Nanyang, China.

出版信息

Bioorg Med Chem Lett. 2015 Jun 15;25(12):2550-4. doi: 10.1016/j.bmcl.2015.04.049. Epub 2015 Apr 23.

Abstract

The strong haemolytic activity of Pulsatilla saponin A (PSA), D (PSD) hampered their clinical development of antitumor agents. In order to solve this problem, C-28 position modification derivatives of PSA/PSD were synthesized. The cytotoxicity and haemolytic activity of these compounds were evaluated. Structure-activity relationship and structure-toxicity relationship had been observed. The mice acute toxicity of compound 11 was reduced greatly than that of PSA. This study indicates that compound 11 may represent an interesting class of potent antitumor agents from triterpenoid saponins avoiding the haemolysis problem. The present study has important significance for the development of antitumor saponins.

摘要

白头翁皂苷A(PSA)、D(PSD)的强溶血活性阻碍了它们作为抗肿瘤药物的临床开发。为了解决这个问题,合成了PSA/PSD的C-28位修饰衍生物。评估了这些化合物的细胞毒性和溶血活性。观察到了构效关系和构毒关系。化合物11的小鼠急性毒性比PSA大大降低。本研究表明,化合物11可能代表一类有趣的、有效的三萜皂苷类抗肿瘤药物,可避免溶血问题。本研究对抗肿瘤皂苷的开发具有重要意义。

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