达沙替尼
化学
髓系白血病
体外
细胞培养
K562细胞
U937电池
立体化学
白血病
IC50型
细胞生长
药理学
癌症研究
生物化学
酪氨酸激酶
免疫学
受体
生物
遗传学
作者
Jin Cai,Shaoning Zhang,Minghao Zheng,Xiaoqing Wu,Junqing Chen,Min Ji
标识
DOI:10.1016/j.bmcl.2011.12.070
摘要
Two series of novel Dasatinib derivatives have been designed and synthesized, with their in vitro cytostatic effect screened on human chronic myeloid leukemia cell line K562 and human myeloid leukemia cell line U937. Some target compounds demonstrated significant inhibitory activities against both cell lines. Compared to the contrast drug Dasatinib, 1b, 1c, 1d, 1e and 1f were found to demonstrate more potent antitumor activities. The structures of all the newly synthesized compounds were determined by 1H NMR and 13C NMR.
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