化学
苏氨酸
结直肠癌
降级(电信)
体内
酪氨酸激酶
癌症研究
酪氨酸
癌症
药理学
生物化学
激酶
蛋白酶体
磷酸化
内科学
信号转导
医学
生物
遗传学
丝氨酸
电信
计算机科学
作者
Jibu Lu,Yong-Jun Huang,Jing Huang,Rui He,Minhao Huang,Xiaoyun Lu,Yong Xu,Fengtao Zhou,Zhang Zhang,Ke Ding
标识
DOI:10.1021/acs.jmedchem.1c01768
摘要
The first examples of threonine tyrosine kinase (TTK) PROTACs were designed and synthesized. Two of the most potent molecules, 8e and 8j, demonstrated strong TTK degradation in COLO-205 human colorectal cancer cells with DC50 values of 1.7 and 3.1 nM, respectively. Proteasome-mediated degradation by the compounds could last for approximately 8 h after washout. The degraders 8e and 8j demonstrated improved antiproliferative activities comparing with the structurally similar inhibitor counterparts 8q and 8r. Degraders 8e and 8j also demonstrated reasonable PK profiles and exhibited potent target degradation and in vivo anticancer efficacy in a xenograft mouse model of COLO-205 human colorectal cancer cells upon i.p. administration.
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