Reaction Details | |||
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Target | E3 ubiquitin-protein ligase Mdm2 | ||
Ligand | BDBM135406 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | FRET Assay | ||
IC50 | 1±n/a nM | ||
Citation | Christopher, MP; Fradera Llinas, FX; Machacek, M; Martinez, M; Reutershan, MH; Shizuka, M; Sun, B; Thompson, CF; Trotter, BW; Voss, ME; Altman, MD; Bogen, SL; Doll, RJ Substituted imidazopyridines as HDM2 inhibitors US Patent US8846657 Publication Date 9/30/2014 | ||
More Info.: | Get all data from this article, Assay Method | ||
E3 ubiquitin-protein ligase Mdm2 | |||
Name: | E3 ubiquitin-protein ligase Mdm2 | ||
Synonyms: | Double minute 2 protein | Double minute 2 protein (HDM2) | E3 ubiquitin-protein ligase Mdm2 (p53-binding protein Mdm2) | Hdm2 | Human Double Minute 2 (HDM2) | MDM2 | MDM2-MDMX | MDM2_HUMAN | p53-Binding Protein MDM2 | p53-binding protein | ||
Type: | Oncoprotein | ||
Mol. Mass.: | 55196.54 | ||
Organism: | Homo sapiens (Human) | ||
Description: | Q00987 | ||
Residue: | 491 | ||
Sequence: |
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BDBM135406 | |||
n/a | |||
Name | BDBM135406 | ||
Synonyms: | US8846657, 13.1 | ||
Type | Small organic molecule | ||
Emp. Form. | C28H35ClN6O4S | ||
Mol. Mass. | 587.133 | ||
SMILES | C[C@H]1CC[C@H](Cn2c(nc3cc(nc(-c4cncc(Cl)c4)c23)C(=O)NS(C)(=O)=O)N2CCO[C@@H]3CCC[C@@H]23)CC1 |r,wU:1.0,33.36,wD:4.4,37.39,(7.91,-3.1,;6.42,-2.7,;5.33,-3.79,;3.84,-3.39,;3.45,-1.9,;1.96,-1.51,;1.56,-.02,;2.46,1.23,;1.56,2.47,;.09,2,;-1.24,2.77,;-2.57,2,;-2.57,.46,;-1.24,-.31,;-1.24,-1.85,;.09,-2.62,;.09,-4.16,;-1.24,-4.93,;-2.57,-4.16,;-3.91,-4.93,;-2.57,-2.62,;.09,.46,;-3.91,2.77,;-3.91,4.31,;-5.24,2,;-6.57,2.77,;-7.91,2,;-7.34,4.1,;-5.8,4.1,;4,1.23,;4.77,-.11,;6.31,-.11,;7.08,1.23,;6.31,2.56,;6.79,4.03,;5.54,4.93,;4.3,4.03,;4.77,2.56,;4.53,-.81,;6.02,-1.21,)| | ||
Structure |