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Discovery of Potent and Selective p53-MDM2 Protein-Protein Interaction Inhibitors as Anticancer Drugs
被引:16
|作者:
Holzer, Philipp
[1
]
机构:
[1] Novartis Inst BioMed Res, CH-4002 Basel, Switzerland
来源:
关键词:
Clinical trial;
HDM2;
Inhibitor;
MDM2;
NVP-CGM097;
NVP-HDM201;
p53;
Protein-protein interaction;
PPI;
STRUCTURE-BASED DESIGN;
P53;
PATHWAY;
MDM2-P53;
INTERACTION;
HIGHLY POTENT;
ANTAGONISTS;
CANCER;
TUMORS;
D O I:
10.2533/chimia.2017.716
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
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.
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页码:716 / 721
页数:6
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