Huang Peter Q, Boren Brant C, Hegde Sayee G, Liu Hui, Unni Aditya K, Abraham Sunny, Hopkins Chad D, Paliwal Sunil, Samatar Ahmed A, Li Jiali, Bunker Kevin D
Zentalis Pharmaceuticals, San Diego, California 92121, United States.
J Med Chem. 2021 Sep 9;64(17):13004-13024. doi: 10.1021/acs.jmedchem.1c01121. Epub 2021 Aug 23.
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 , a highly selective Wee1 inhibitor with balanced potency, ADME, and pharmacokinetic properties. The chiral ethyl moiety of compound provided an unexpected improvement of Wee1 potency. Compound , known as ZN-c3, showed excellent efficacy and is currently being evaluated in phase 2 clinical trials.
在过去十年中,Wee1抑制作为一种有前景的癌症治疗方法受到了极大关注。因此,一种强效且选择性的Wee1抑制剂是非常需要的。我们致力于研发更安全、更有效的Wee1抑制剂,从而发现了化合物 ,这是一种具有平衡效力、药物代谢动力学性质和药代动力学性质的高选择性Wee1抑制剂。化合物 的手性乙基部分使Wee1效力得到了意外的提高。化合物 ,即ZN-c3,显示出优异的疗效,目前正在进行2期临床试验评估。