广告
第1周
化学
效力
药理学
体内
药代动力学
临床试验
医学
体外
内科学
生物化学
细胞周期
生物技术
生物
细胞周期蛋白依赖激酶1
细胞
作者
Peter Q. Huang,Brant C. Boren,Sayee G. Hegde,Hui Liu,Aditya K. Unni,Sunny Abraham,Chad D. Hopkins,Sunil Paliwal,Ahmed A. Samatar,Jiali Li,Kevin D. Bunker
标识
DOI:10.1021/acs.jmedchem.1c01121
摘要
Wee1 inhibition has received great attention in the past decade as a promising therapy for cancer treatment. Therefore, a potent and selective Wee1 inhibitor is highly desirable. Our efforts to make safer and more efficacious Wee1 inhibitors led to the discovery of compound 16, a highly selective Wee1 inhibitor with balanced potency, ADME, and pharmacokinetic properties. The chiral ethyl moiety of compound 16 provided an unexpected improvement of Wee1 potency. Compound 16, known as ZN-c3, showed excellent in vivo efficacy and is currently being evaluated in phase 2 clinical trials.
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