null

SMILES [H][C@]12C[C@]3([H])C[C@]([H])(C1)CC(CN1c4ccccc4N(c4ccccc4)C(=O)C(NC(=O)Nc4ccc(Br)cc4)C1=O)(C2)C3

InChI Key InChIKey=WEJAEIIVFZYFGG-BNQLQADTSA-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 2 hits for monomerid = 50472874   

TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
Glaxo Wellcome Medicines Research Centre

Curated by ChEMBL
LigandPNGBDBM50472874(CHEMBL118189)copy SMILEScopy InChI
Affinity DataKi:  1.40nMAssay Description:In vitro inhibition of binding of [3H]pCCK-8 against Cholecystokinin type B receptor of guinea pig cerebral cortex membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26H4M5VPubMed
TargetCholecystokinin receptor type A(RAT)
Glaxo Wellcome Medicines Research Centre

Curated by ChEMBL
LigandPNGBDBM50472874(CHEMBL118189)copy SMILEScopy InChI
Affinity DataKi:  3.47E+3nMAssay Description:In vitro inhibition of binding of [3H]pCCK-8 against Cholecystokinin type A receptor of rat pancreatic membranesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q26H4M5VPubMed