BDBM50043486 1-(1-Methyl-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e][1,4]diazepin-3-yl)-3-(1-phenyl-ethyl)-urea::CHEMBL137208

SMILES C[C@H](NC(=O)NC1N=C(c2ccccc2)c2ccccc2N(C)C1=O)c1ccccc1

InChI Key InChIKey=AMJHJWQKGLQESV-NVHKAFQKSA-N

Data  2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50043486   

TargetCholecystokinin receptor type A(RAT)
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50043486(1-(1-Methyl-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e]...)
Show SMILES C[C@H](NC(=O)NC1N=C(c2ccccc2)c2ccccc2N(C)C1=O)c1ccccc1
Show InChI InChI=1S/C25H24N4O2/c1-17(18-11-5-3-6-12-18)26-25(31)28-23-24(30)29(2)21-16-10-9-15-20(21)22(27-23)19-13-7-4-8-14-19/h3-17,23H,1-2H3,(H2,26,28,31)/t17-,23?/m0/s1
Affinity DataIC50: 430nMAssay Description:Inhibition of binding of [125I]CCK-8 to cholecystokinin type A receptor in rat pancreatic tissueMore data for this Ligand-Target Pair
TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50043486(1-(1-Methyl-2-oxo-5-phenyl-2,3-dihydro-1H-benzo[e]...)
Show SMILES C[C@H](NC(=O)NC1N=C(c2ccccc2)c2ccccc2N(C)C1=O)c1ccccc1
Show InChI InChI=1S/C25H24N4O2/c1-17(18-11-5-3-6-12-18)26-25(31)28-23-24(30)29(2)21-16-10-9-15-20(21)22(27-23)19-13-7-4-8-14-19/h3-17,23H,1-2H3,(H2,26,28,31)/t17-,23?/m0/s1
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of binding of [125I]-CCK-8 to the cholecystokinin type B receptorMore data for this Ligand-Target Pair