Discovery of chromeno”4,3-c”pyrazol-4(2H)-one containing carbonyl or oxime derivatives as potential,selective inhibitors PI3Kα
A series of novel chromeno”4,3-c”pyrazol-4(2H)-one containing carbonyl or oxime derivatives(4a-4n,5a-5n)have been synthesized and evaluated their biological activities as PI3K inhibitors.Out of them,compound 5l showed the most potent antiproliferative activities against HCT-116 with IC50 of 0.10 μM in vitro,and exhibited the most potent activity for PI3Kα with the value of 0.012 μM.Docking simulation of 51 into PI3Kα active site were performed to determine the probable binding model,and it indicated that compound 5l could be optimized as a potential inhibitor of PI3Kα in the further study.
chromeno”4,3-c”pyrazol-4(2H)-one derivatives PI3Kα Antiproliferative
Liang Lu Shao Sha Kai Wang Yuan-Heng Zhang Yan-Dong Liu Guo-Dong Ju Baozhong Wang Hai-Liang Zhu
State Key Laboratory of Pharmaceutical Biotechnology,Nanjing University,Nanjing 210093,People”s Republic of China
国内会议
大连
英文
289-309
2016-09-24(万方平台首次上网日期,不代表论文的发表时间)