null

SMILES Cc1nc(NC(=O)c2ccccc2)sc1C(=O)Nc1c(C)cc(C)cc1C

InChI Key InChIKey=LEOANBUEWRQPOF-UHFFFAOYSA-N

  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 4 hits for monomerid = 13224   

TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM13224(2-N-benzene-4-methyl-5-N-(2,4,6-trimethylphenyl)-1...)copy SMILEScopy InChI
Affinity DataIC50: 800nMpH: 7.0 T: 2°CAssay Description:IC50 is the inhibitor concentration, which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-33P] lab...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QN6501PubMed
TargetProto-oncogene tyrosine-protein kinase LCK(Mus musculus)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM13224(2-N-benzene-4-methyl-5-N-(2,4,6-trimethylphenyl)-1...)copy SMILEScopy InChI
Affinity DataIC50: 320nMAssay Description:In vitro inhibition of murine Lck kinase.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CC103JPubMed
TargetTyrosine-protein kinase Lck(Homo sapiens (Human))
Bristol-Myers Squibb Company

LigandPNGBDBM13224(2-N-benzene-4-methyl-5-N-(2,4,6-trimethylphenyl)-1...)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibitory activity of the compound human Lck(hLck) kinaseMore data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2CC103JPubMed
TargetProto-oncogene tyrosine-protein kinase LCK(Mus musculus)
Bristol-Myers Squibb Pharmaceutical Research Institute

Curated by ChEMBL
LigandPNGBDBM13224(2-N-benzene-4-methyl-5-N-(2,4,6-trimethylphenyl)-1...)copy SMILEScopy InChI
Affinity DataIC50: 320nMpH: 7.0 T: 2°CAssay Description:IC50 is the inhibitor concentration, which inhibits 50% of kinase activity that catalyzes the transfer of the terminal phosphate from [gamma-33P] lab...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2QN6501PubMed