Discovery of AMG 232, a Potent, Selective, and Orally Bioavailable MDM2–p53 Inhibitor in Clinical Development

Author:

Sun Daqing123,Li Zhihong123,Rew Yosup123,Gribble Michael123,Bartberger Michael D.123,Beck Hilary P.123,Canon Jude123,Chen Ada123,Chen Xiaoqi123,Chow David123,Deignan Jeffrey123,Duquette Jason123,Eksterowicz John123,Fisher Benjamin123,Fox Brian M.123,Fu Jiasheng123,Gonzalez Ana Z.123,Gonzalez-Lopez De Turiso Felix123,Houze Jonathan B.123,Huang Xin123,Jiang Min123,Jin Lixia123,Kayser Frank123,Liu Jiwen (Jim)123,Lo Mei-Chu123,Long Alexander M.123,Lucas Brian123,McGee Lawrence R.123,McIntosh Joel123,Mihalic Jeff123,Oliner Jonathan D.123,Osgood Tao123,Peterson Matthew L.123,Roveto Philip123,Saiki Anne Y.123,Shaffer Paul123,Toteva Maria123,Wang Yingcai123,Wang Yu Chung123,Wortman Sarah123,Yakowec Peter123,Yan Xuelei123,Ye Qiuping123,Yu Dongyin123,Yu Ming123,Zhao Xiaoning123,Zhou Jing123,Zhu Jiang123,Olson Steven H.123,Medina Julio C.123

Affiliation:

1. Departments of Therapeutic Discovery, ‡Pharmaceutics, and §Pharmacokinetics and Drug Metabolism, Amgen Inc., 1120 Veterans Boulevard, South San Francisco, California, 94080, United States

2. Departments of Therapeutic Discovery, and ⊥Oncology Research, Amgen Inc., One Amgen Center Drive, Thousand Oaks, California 91320, United States

3. Departments of Therapeutic Discovery, and ∇Pharmaceutics, Amgen Inc., 360 Binney Street, Cambridge, Massachusetts 02142, United States

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

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