Novel Lycorine Derivatives as Anticancer Agents: Synthesis and In Vitro Biological Evaluation
作者:Peng Wang、Hui-Hui Yuan、Xue Zhang、Yun-Ping Li、Lu-Qing Shang、Zheng Yin
DOI:10.3390/molecules19022469
日期:——
Lycorine, which is the most abundant alkaloid isolated from the Amaryllidaceae family of plants, reportedly exhibits promising anticancer activities. Herein, a series of novel lycorine derivatives were synthesized and evaluated for their in vitro inhibitory activities against seven different cancer cell lines, including A549, HCT116, SK-OV-3, NCI-H460, K562, MCF-7 and HL-60. The results indicated that compounds bearing diverse amine substituents at the C-2 position demonstrated good anticancer activities. The selectivity towards different cancer cell lines of the synthesized derivatives is discussed.
据报道,番荔枝碱是从金盏花科植物中分离出来的最丰富的生物碱,具有良好的抗癌活性。本文合成了一系列新型番茄红素衍生物,并评估了它们对七种不同癌细胞株(包括 A549、HCT116、SK-OV-3、NCI-H460、K562、MCF-7 和 HL-60)的体外抑制活性。结果表明,C-2 位上带有不同胺取代基的化合物具有良好的抗癌活性。本文还讨论了合成的衍生物对不同癌细胞系的选择性。