Structure-Based Design of Potent and Orally Active Isoindolinone Inhibitors of MDM2-p53 Protein–Protein Interaction

Author:

Chessari Gianni1ORCID,Hardcastle Ian R.2ORCID,Ahn Jong Sook1,Anil Burcu3,Anscombe Elizabeth3,Bawn Ruth H.2,Bevan Luke D.1,Blackburn Timothy J.2,Buck Ildiko1,Cano Celine2ORCID,Carbain Benoit2,Castro Juan1,Cons Ben1,Cully Sarah J.2,Endicott Jane A.4,Fazal Lynsey1,Golding Bernard T.2,Griffin Roger J.2,Haggerty Karen2,Harnor Suzannah J.2ORCID,Hearn Keisha1,Hobson Stephen2,Holvey Rhian S.1,Howard Steven1,Jennings Claire E.4,Johnson Christopher N.1ORCID,Lunec John4,Miller Duncan C.2ORCID,Newell David R.4,Noble Martin E. M.4,Reeks Judith1,Revill Charlotte H.2,Riedinger Christiane3,St. Denis Jeffrey D.1,Tamanini Emiliano1ORCID,Thomas Huw4,Thompson Neil T.1,Vinković Mladen1,Wedge Stephen R.4,Williams Pamela A.1,Wilsher Nicola E.1,Zhang Bian2,Zhao Yan4

Affiliation:

1. Astex Pharmaceuticals, 436 Cambridge Science Park, Milton Road, Cambridge CB4 0QA, U.K.

2. Cancer Research UK Newcastle Drug Discovery Unit, Newcastle University Centre for Cancer, Chemistry, School of Natural and Environmental Sciences, Newcastle University, Bedson Building, Newcastle upon Tyne NE1 7RU, U.K.

3. Department of Biochemistry, University of Oxford, South Parks Road, Oxford OX1 3QU, U.K.

4. Cancer Research UK Newcastle Drug Discovery Unit, Translational and Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Paul O’Gorman Building, Newcastle upon Tyne NE2 4HH, U.K.

Funder

Cancer Research UK

Publisher

American Chemical Society (ACS)

Subject

Drug Discovery,Molecular Medicine

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