Reaction Details | |||
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Target | E3 ubiquitin-protein ligase Mdm2 [17-125] | ||
Ligand | BDBM223681 | ||
Substrate/Competitor | n/a | ||
Meas. Tech. | FRET Assay | ||
Temperature | 298.15±n/a K | ||
IC50 | 0.5071±n/a nM | ||
Comments | extracted | ||
Citation | Cammarano, CM; Christopher, MP; Dinsmore, C; Doll, RJ; Fradera Llinas, FX; Li, C; Machacek, M; Martinez, M; Nair, LG; Pan, W; Reutershan, MH; Shizuka, M; Steinhuebel, DP; Sun, B; Thompson, CF; Trotter, BW; Wang, Y; Yang, L; Bogen, SL; Voss, ME; Panda, J; Kurissery, AT 2,6,7,8 substituted purines as HDM2 inhibitors US Patent US9540377 Publication Date 1/10/2017 | ||
More Info.: | Get all data from this article, Assay Method | ||
E3 ubiquitin-protein ligase Mdm2 [17-125] | |||
Name: | E3 ubiquitin-protein ligase Mdm2 [17-125] | ||
Synonyms: | Double minute 2 protein | E3 ubiquitin-protein ligase Mdm2 | MDM2 | MDM2_HUMAN | p53-binding protein Mdm2 | ||
Type: | Enzyme Catalytic Domain | ||
Mol. Mass.: | 12522.24 | ||
Organism: | Homo sapiens (Human) | ||
Description: | Residue 17 to 125 | ||
Residue: | 109 | ||
Sequence: |
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BDBM223681 | |||
n/a | |||
Name | BDBM223681 | ||
Synonyms: | 3-(6-{[(1r)-1- cyclobutylethyl]amino}- 8-[2-(1-methoxy- 1- methylethyl)pyrrolidin- 1-yl]-7-[(trans-4- methylcyclohexyl) methyl]-7h-purin-2- yl)-1,2,4-oxadiazol- 5(2h)-one | US9540377, 11.107 | ||
Type | Small organic molecule | ||
Emp. Form. | C29H44N8O3 | ||
Mol. Mass. | 552.7115 | ||
SMILES | COC(C)(C)C1CCCN1c1nc2nc(nc(N[C@H](C)C3CCC3)c2n1C[C@H]1CC[C@H](C)CC1)-c1noc(=O)[nH]1 |r,wU:18.19,30.34,wD:27.30,(3.53,6.41,;4.3,5.07,;3.53,3.74,;1.99,3.74,;2.76,5.07,;4.3,2.41,;5.77,1.93,;5.77,.39,;4.3,-.09,;3.4,1.16,;1.86,1.16,;.95,2.41,;-.51,1.93,;-1.85,2.7,;-3.18,1.93,;-3.18,.39,;-1.85,-.38,;-1.85,-1.92,;-3.18,-2.69,;-4.51,-1.92,;-3.18,-4.23,;-4.27,-5.32,;-3.18,-6.41,;-2.09,-5.32,;-.51,.39,;.95,-.09,;1.35,-1.57,;2.84,-1.97,;3.24,-3.46,;4.72,-3.86,;5.81,-2.77,;7.3,-3.17,;5.41,-1.28,;3.93,-.88,;-4.51,2.7,;-5.76,1.8,;-7.01,2.7,;-6.53,4.17,;-7.3,5.5,;-4.99,4.17,)| | ||
Structure |