靛玉红
化学
酶
抑制性突触后电位
衍生工具(金融)
K562细胞
肿瘤细胞
生物化学
立体化学
组合化学
体外
生物
医学
癌症研究
内科学
靛蓝
艺术
金融经济学
经济
视觉艺术
作者
Bin Sun,Jiahao Wang,Luohua Liu,Longfei Mao,Lizeng Peng,Yuwei Wang
摘要
Abstract A series of indirubin derivatives hydrochloride were obtained using a convenient and mild method from indirubin. The newly synthesized compounds and their derivatives were characterized by 1 H NMR, 13 C NMR, and MS. Furthermore, we tested their IDO1 enzyme inhibitory activity and anti‐proliferative activities in K562 tumor cells. The experimental results revealed that some of the compounds showed potential anti‐enzyme and anti‐tumor activity. Among of them, compound 4b exhibited certain inhibitory activity on IDO1 (IC 50 : 29.52 μmol/L), and compound 4a displayed activity similar to indirubin in K562 tumor cells (IC 50 : 24.96 μmol/L). This type of indirubin derivative is expected to have the potential to act as an immunologically active anti‐tumor drug, indicating that further research will be worthwhile.
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