喹啉
泛素连接酶
化学
细胞毒性T细胞
DNA连接酶
平方毫米
立体化学
IC50型
体外
抑制性突触后电位
生物化学
细胞毒性
泛素
生物
酶
有机化学
细胞凋亡
神经科学
基因
作者
Xiaoxue Dou,Xin Li,Tao Liu,Chunqi Hu,Lei Zhang,Qiaojun He,Bo Yang,Yongzhou Hu
出处
期刊:Medicinal Chemistry
日期:2013-04-01
卷期号:9 (4): 581-587
被引量:4
标识
DOI:10.2174/1573406411309040012
摘要
A series of pyrimido[4,5-b]quinoline-2,4-dione derivatives was synthesized and evaluated for their cytotoxic activities in vitro against five human cancer cell lines. Selected compounds were tested for their MDM2 E3 ligase inhibitory activities and p53-MDM2 binding inhibitory activities. Among tested compounds, four sulfur-containing compounds (4-7) displayed enhanced cytotoxic activities and better MDM2 E3 ligase inhibitoty activities in comparison with that of HLI98c. Three compounds (4-6) showed better p53-MDM2 binding inhibitory potency with IC50 values ranging from 1.3 μM to 9.0 μM. Keywords: Cytotoxic activity, MDM2 E3 ligase inhibitory activity, p53-MDM2 binding inhibitor, pyrimido[4, 5-b]quinoline- 2, 4-dione
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