化学
吡唑
蛋白激酶B
噻吩
体外
细胞凋亡
激酶
立体化学
IC50型
磷酸化
结构-活动关系
细胞生长
癌细胞
细胞培养
药理学
生物化学
癌症
生物
有机化学
遗传学
作者
Wenhu Zhan,Jinxin Che,Lei Xu,Yizhe Wu,Xiaobei Hu,Yubo Zhou,Gang Cheng,Yongzhou Hu,Xiaowu Dong,Jia Li
标识
DOI:10.1016/j.ejmech.2019.07.017
摘要
A series of pyrazole-thiophene derivatives exhibiting good Akt inhibitory activities were obtained on the basis of conformational restriction strategy, leading to the discovery of compound 1d and 1o which showed excellent in vitro antitumor effect against a variety of hematologic cancer cells and their potential of inducing apoptosis, blocking the cell cycles at S phase and significantly inhibiting the phosphorylation of downstream biomarkers of Akt kinase of cancer cells. Amongst, compound 1o also exhibited good PK profiles and inhibited about 40% tumor growth in MM1S xenograft model. Compound 1o might be a potential candidate for further development.
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