Selective and potent morpholinone inhibitors of the MDM2-p53 interaction

被引:0
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作者
Gonzalez, Ana Z. [1 ]
Eksterowics, John [1 ]
Beck, Hilary P. [1 ]
Canon, Jude [4 ]
Chen, Ada [1 ]
Chow, David [1 ]
Duquette, Jason [1 ]
Fox, Brian M. [1 ]
Fu, Jiasheng [1 ]
Houze, Jonathan [1 ]
Jin, Lixia [1 ]
Li, Yihong [1 ]
Li, Zhihong [1 ]
Lo, Mei-Chu [1 ]
Long, Alexander M. [5 ]
McGee, Lawrence R. [1 ]
McIntosh, Joel [1 ]
Oliner, Jonathan D. [4 ]
Osgood, Tao [4 ]
Rew, Yosup [1 ]
Saiki, Anne Y. [4 ]
Shaffer, Paul [5 ]
Wortman, Sarah [2 ]
Yakowek, Peter [5 ]
Yan, Xuelei [1 ]
Ye, Qiuping [3 ]
Yu, Dongyin [4 ]
Zhao, Xiaoning [1 ]
Zhou, Jing [1 ]
Olson, Steven H. [1 ]
Medina, Julio C. [1 ]
Sun, Daqing [1 ]
机构
[1] Amgen Inc, Dept Therapeut Discovery, San Francisco, CA 94080 USA
[2] Amgen Inc, Pharmaceut, San Francisco, CA 94080 USA
[3] Amgen Inc, Dept Therapeut Discovery, Thousand Oaks, CA 91320 USA
[4] Amgen Inc, Oncol Res, Thousand Oaks, CA 91320 USA
[5] Amgen Inc, Dept Therapeut Discovery, Cambridge, MA 02142 USA
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中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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页数:1
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