jm401753e_si_001.pdf (202.36 kB)
Discovery of AMG 232, a Potent, Selective, and Orally Bioavailable MDM2–p53 Inhibitor in Clinical Development
journal contribution
posted on 2014-02-27, 00:00 authored by Daqing Sun, Zhihong Li, Yosup Rew, Michael Gribble, Michael
D. Bartberger, Hilary P. Beck, Jude Canon, Ada Chen, Xiaoqi Chen, David Chow, Jeffrey Deignan, Jason Duquette, John Eksterowicz, Benjamin Fisher, Brian M. Fox, Jiasheng Fu, Ana Z. Gonzalez, Felix Gonzalez-Lopez De Turiso, Jonathan B. Houze, Xin Huang, Min Jiang, Lixia Jin, Frank Kayser, Jiwen
(Jim) Liu, Mei-Chu Lo, Alexander M. Long, Brian Lucas, Lawrence
R. McGee, Joel McIntosh, Jeff Mihalic, Jonathan D. Oliner, Tao Osgood, Matthew
L. Peterson, Philip Roveto, Anne Y. Saiki, Paul Shaffer, Maria Toteva, Yingcai Wang, Yu Chung Wang, Sarah Wortman, Peter Yakowec, Xuelei Yan, Qiuping Ye, Dongyin Yu, Ming Yu, Xiaoning Zhao, Jing Zhou, Jiang Zhu, Steven
H. Olson, Julio C. MedinaWe
recently reported the discovery of AM-8553 (1),
a potent and selective piperidinone inhibitor of the MDM2–p53
interaction. Continued research investigation of the N-alkyl substituent of this series, focused in particular on a previously
underutilized interaction in a shallow cleft on the MDM2 surface,
led to the discovery of a one-carbon tethered sulfone which gave rise
to substantial improvements in biochemical and cellular potency. Further
investigation produced AMG 232 (2), which is currently
being evaluated in human clinical trials for the treatment of cancer.
Compound 2 is an extremely potent MDM2 inhibitor (SPR KD = 0.045 nM, SJSA-1 EdU IC50 = 9.1
nM), with remarkable pharmacokinetic properties and in vivo antitumor
activity in the SJSA-1 osteosarcoma xenograft model (ED50 = 9.1 mg/kg).