BDBM6678 3-[(2-chloro-6-fluorophenyl)carbonyl]-6-[(2,6-difluorophenyl)carbonyl]imidazo[1,2-a]pyridin-2-amine::aminoimidazo[1,2-a]pyridine deriv. 15

SMILES Nc1nc2ccc(cn2c1C(=O)c1c(F)cccc1Cl)C(=O)c1c(F)cccc1F

InChI Key InChIKey=BBACZASSMOBONU-UHFFFAOYSA-N

Data  3 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 6678   

TargetCyclin-dependent kinase 2/G1/S-specific cyclin-E1(Homo sapiens (Human))
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LigandPNGBDBM6678(3-[(2-chloro-6-fluorophenyl)carbonyl]-6-[(2,6-difl...)
Affinity DataIC50:  102nMpH: 7.0 T: 2°CAssay Description:In vitro CDK assay using purified enzyme, was incubated at room temperature with substrate, and test compounds in the presence of ATP/[gamma-33P]ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 4/G1/S-specific cyclin-D1(Homo sapiens (Human))
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LigandPNGBDBM6678(3-[(2-chloro-6-fluorophenyl)carbonyl]-6-[(2,6-difl...)
Affinity DataIC50:  827nMT: 2°CAssay Description:In vitro CDK assay using purified enzyme, was incubated at room temperature with substrate, and test compounds in the presence of ATP/[gamma-33P]ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase/G2/mitotic-specific cyclin- 1(Homo sapiens (Human))
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LigandPNGBDBM6678(3-[(2-chloro-6-fluorophenyl)carbonyl]-6-[(2,6-difl...)
Affinity DataIC50:  239nMT: 2°CAssay Description:In vitro CDK assay using purified enzyme, was incubated at room temperature with substrate, and test compounds in the presence of ATP/[gamma-33P]ATP....More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed