Fragment-based discovery of a highly potent, orally bioavailable ERK1/2 inhibitor that modulates the phosphorylation and catalytic activity of ERK1/2

被引:0
|
作者
Heightman, Tom D. [1 ]
Berdini, Valerio [1 ]
Braithwaite, Hannah [1 ]
Buck, Ildiko [1 ]
Cassidy, Megan [1 ]
Castro, Juan [1 ]
Courtin, Aurelie [1 ]
Day, James [1 ]
East, Charlotte [1 ]
Fazal, Lynsey [1 ]
Graham, Brent [1 ]
Griffiths-Jones, Charlotte [1 ]
Lyons, John [1 ]
Martins, Vanessa [1 ]
Muench, Sandra [1 ]
Munck, Joanne [1 ]
Norton, David [1 ]
O'Reilly, Marc [1 ]
Palmer, Nick [1 ]
Pathuri, Puja [1 ]
Reader, Mike [1 ]
Rees, David [1 ]
Rich, Sharna [1 ]
Richardson, Caroline [1 ]
Saini, Harpreet [1 ]
Thompson, Neil [1 ]
Wallis, Nicola [1 ]
Walton, Hugh [1 ]
Wilsher, Nicola [1 ]
Woolford, Alison [1 ]
Murray, Chris [1 ]
机构
[1] Astex Pharmaceut Inc, Cambridge, England
关键词
D O I
10.1158/1535-7163.TARG-17-B161
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
B161
引用
收藏
页数:2
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