王永成, 李玉山, 杨瀚泽, 李燕, 陈晓光, 冯志强. 新型姜黄素类似物的合成及初步抗肿瘤活性研究J. 药学学报, 2014,49(7): 1022-1028.
引用本文: 王永成, 李玉山, 杨瀚泽, 李燕, 陈晓光, 冯志强. 新型姜黄素类似物的合成及初步抗肿瘤活性研究J. 药学学报, 2014,49(7): 1022-1028.
WANG Yong-cheng, LI Yu-shan, YANG Han-ze, LI Yan, CHEN Xiao-guang, FENG Zhi-qiang. Synthesis of novel curcumin mimics and preliminary evaluation for their antitumor activityJ. Acta Pharmaceutica Sinica, 2014,49(7): 1022-1028.
Citation: WANG Yong-cheng, LI Yu-shan, YANG Han-ze, LI Yan, CHEN Xiao-guang, FENG Zhi-qiang. Synthesis of novel curcumin mimics and preliminary evaluation for their antitumor activityJ. Acta Pharmaceutica Sinica, 2014,49(7): 1022-1028.

新型姜黄素类似物的合成及初步抗肿瘤活性研究

Synthesis of novel curcumin mimics and preliminary evaluation for their antitumor activity

  • 摘要: 姜黄素具有明确的抗肿瘤活性和很好的安全性,然而它的结构的不稳定性和较差的药代学性质一定程度上限制了其临床应用。为了克服这些缺点,寻找具有更好抗肿瘤活性的小分子,本文设计合成了29个新型姜黄素类似物,通过1H NMR和HR-MS确定了其化学结构,并测试了它们对5个肿瘤细胞株的体外抗增殖活性。初步药理活性研究结果表明,化合物16、18、19具有较好的抗肿瘤活性,对多种细胞株的IC50值低于5 μmol·L-1,是姜黄素的5~9倍。

     

    Abstract: Curcumin has been reported to possess antitumor activity with low toxicity. However, the clinical application of curcumin has been significantly limited by its instability and poor metabolic property. In order to overcome these limitations and discover novel small molecules with potential antitumor activity, 29 curcumin mimics were synthesized, which were confirmed by 1H NMR and HR-MS, and their cytotoxic property was evaluated against five human cancer cell lines in vitro. Compounds 16, 18 and 19 exhibited good cytotoxic property, their IC50 value were even below 5 μmol·L-1 to some cancer cell lines, 5-9 times better than curcumin.

     

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