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发现强效且选择性的p53-MDM2蛋白-蛋白相互作用抑制剂作为抗癌药物

Discovery of Potent and Selective p53-MDM2 Protein-Protein Interaction Inhibitors as Anticancer Drugs.

作者信息

Holzer Philipp

机构信息

Novartis Institutes for BioMedical Research CH-4002 Basel;, Email:

出版信息

Chimia (Aarau). 2017 Oct 25;71(10):716-721. doi: 10.2533/chimia.2017.716.

Abstract

As a result of our persistent efforts to discover novel inhibitors of the p53-MDM2 protein-protein interaction useful for the treatment of cancer, the potent and selective MDM2 inhibitors NVP-CGM097 and NVP-HDM201 with excellent in vitro and in vivo profile were selected as clinical candidates and are currently in phase 1 clinical development. This short review article provides a summary of the program history, the applied pharmacophore model and the discovery story of these novel p53-MDM2 inhibitor investigational drugs.

摘要

由于我们持续努力发现可用于癌症治疗的新型p53-MDM2蛋白-蛋白相互作用抑制剂,强效且选择性的MDM2抑制剂NVP-CGM097和NVP-HDM201凭借出色的体外和体内活性被选为临床候选药物,目前正处于1期临床开发阶段。这篇简短的综述文章总结了该项目历程、应用的药效团模型以及这些新型p53-MDM2抑制剂研究药物的发现过程。

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