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TargetCyclin-dependent kinase 4
LigandBDBM50293153
Substrate/Competitorn/a
Meas. Tech.ChEMBL_496923 (CHEMBL1002018)
IC50 0.3±n/a nM
Citation Stevens, KLReno, MJAlberti, JBPrice, DJKane-Carson, LSKnick, VBShewchuk, LMHassell, AMVeal, JMDavis, STGriffin, RJPeel, MR Synthesis and evaluation of pyrazolo[1,5-b]pyridazines as selective cyclin dependent kinase inhibitors. Bioorg Med Chem Lett18:5758-62 (2009) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Cyclin-dependent kinase 4
Name:Cyclin-dependent kinase 4
Synonyms:CDK4 | CDK4_HUMAN | Cell division protein kinase 4 | Cyclin-dependent kinase 4 (CDK 4) | PSK-J3
Type:Enzyme Subunit
Mol. Mass.:33731.96
Organism:Homo sapiens (Human)
Description:P11802
Residue:303
Sequence:
MATSRYEPVAEIGVGAYGTVYKARDPHSGHFVALKSVRVPNGGGGGGGLPISTVREVALL
RRLEAFEHPNVVRLMDVCATSRTDREIKVTLVFEHVDQDLRTYLDKAPPPGLPAETIKDL
MRQFLRGLDFLHANCIVHRDLKPENILVTSGGTVKLADFGLARIYSYQMALTPVVVTLWY
RAPEVLLQSTYATPVDMWSVGCIFAEMFRRKPLFCGNSEADQLGKIFDLIGLPPEDDWPR
DVSLPRGAFPPRGPRPVQSVVPEMEESGAQLLLEMLTFNPHKRISAFRALQHSYLHKDEG
NPE
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  Blast E-value cutoff:
BDBM50293153
n/a
NameBDBM50293153
Synonyms:CHEMBL526110 | N-(3-nitrophenyl)-4-(pyrazolo[1,5-b]pyridazin-3-yl)pyrimidin-2-amine | TCMDC-138697
TypeSmall organic molecule
Emp. Form.C16H11N7O2
Mol. Mass.333.3042
SMILES[O-][N+](=O)c1cccc(Nc2nccc(n2)-c2cnn3ncccc23)c1
Structure
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