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TargetE3 ubiquitin-protein ligase Mdm2 [17-125]
LigandBDBM326305
Substrate/Competitorn/a
Meas. Tech.FRET Assay
IC50 6188±n/a nM
Citation Dinsmore, CFradera Llinas, FXKudale, AAMachacek, MReutershan, MHThompson, CFTrotter, BWYang, LAltman, MDBogen, SLDoll, RJVoss, ME Substituted pyrrolopyrimidines as HDM2 inhibitors US Patent US9637493 Publication Date 5/2/2017
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:
SQIPASEQETLVRPKPLLLKLLKSVGAQKDTYTMKEVLFYLGQYIMTKRLYDEKQQHIVY
CSNDLLGDLFGVPSFSVKEHRKIYTMIYRNLVVVNQQESSDSGTSVSEN
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BDBM326305
n/a
NameBDBM326305
Synonyms:4-{[(1R)-1- cyclobutylethyl] amino}-5-(4- methoxybenzyl)-6- (3-methylphenyl)-5H- pyrrolo[3,2- d]pyrimidine-2- carboxylic acid | US9637493, 2.8
TypeSmall organic molecule
Emp. Form.C28H30N4O3
Mol. Mass.470.5628
SMILESCOc1ccc(Cn2c(cc3nc(nc(N[C@H](C)C4CCC4)c23)C(O)=O)-c2cccc(C)c2)cc1 |r|
Structure
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