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7BIV

Inhibitor of MDM2-p53 Interaction

Summary for 7BIV
Entry DOI10.2210/pdb7biv/pdb
DescriptorE3 ubiquitin-protein ligase Mdm2, DIMETHYL SULFOXIDE, 1,2-ETHANEDIOL, ... (6 entities in total)
Functional Keywordsligase, cell cycle, apoptosis, protein binding
Biological sourceHomo sapiens (Human)
Total number of polymer chains1
Total formula weight12127.54
Authors
Williams, P.A. (deposition date: 2021-01-13, release date: 2021-04-07, Last modification date: 2024-05-15)
Primary citationChessari, G.,Hardcastle, I.R.,Ahn, J.S.,Anil, B.,Anscombe, E.,Bawn, R.H.,Bevan, L.D.,Blackburn, T.J.,Buck, I.,Cano, C.,Carbain, B.,Castro, J.,Cons, B.,Cully, S.J.,Endicott, J.A.,Fazal, L.,Golding, B.T.,Griffin, R.J.,Haggerty, K.,Harnor, S.J.,Hearn, K.,Hobson, S.,Holvey, R.S.,Howard, S.,Jennings, C.E.,Johnson, C.N.,Lunec, J.,Miller, D.C.,Newell, D.R.,Noble, M.E.M.,Reeks, J.,Revill, C.H.,Riedinger, C.,St Denis, J.D.,Tamanini, E.,Thomas, H.,Thompson, N.T.,Vinkovic, M.,Wedge, S.R.,Williams, P.A.,Wilsher, N.E.,Zhang, B.,Zhao, Y.
Structure-Based Design of Potent and Orally Active Isoindolinone Inhibitors of MDM2-p53 Protein-Protein Interaction.
J.Med.Chem., 64:4071-4088, 2021
Cited by
PubMed Abstract: Inhibition of murine double minute 2 (MDM2)-p53 protein-protein interaction with small molecules has been shown to reactivate p53 and inhibit tumor growth. Here, we describe rational, structure-guided, design of novel isoindolinone-based MDM2 inhibitors. MDM2 X-ray crystallography, quantum mechanics ligand-based design, and metabolite identification all contributed toward the discovery of potent and inhibitors of the MDM2-p53 interaction with representative compounds inducing cytostasis in an SJSA-1 osteosarcoma xenograft model following once-daily oral administration.
PubMed: 33761253
DOI: 10.1021/acs.jmedchem.0c02188
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.64 Å)
Structure validation

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