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ZN-c3的发现,一种高效且选择性的Wee1抑制剂,正在进行癌症治疗的临床试验评估。

Discovery of ZN-c3, a Highly Potent and Selective Wee1 Inhibitor Undergoing Evaluation in Clinical Trials for the Treatment of Cancer.

作者信息

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

机构信息

Zentalis Pharmaceuticals, San Diego, California 92121, United States.

出版信息

J Med Chem. 2021 Sep 9;64(17):13004-13024. doi: 10.1021/acs.jmedchem.1c01121. Epub 2021 Aug 23.

Abstract

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.

摘要

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。

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