null

SMILES [H][C@]12C[C@]3([H])C[C@]([H])(C1)CC(CNC(=O)C1C(C4c5ccccc5C1c1ccccc41)C(=O)N1CCC[C@H]1C(=O)NCC(O)=O)(C2)C3

InChI Key InChIKey=RRIOZKGLISHEDX-WBBUDUBFSA-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 = 50470628   

TargetGastrin/cholecystokinin type B receptor(MOUSE)
James Black Foundation

Curated by ChEMBL
LigandPNGBDBM50470628(CHEMBL336896)copy SMILEScopy InChI
Affinity DataKi:  138nMAssay Description:Competition with 20 pM [125I]BH-CCK-8S for Cholecystokinin type B receptor binding sites in mouse cortical homogenatesMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930WWVPubMed
TargetCholecystokinin receptor type A(Cavia porcellus)
James Black Foundation

Curated by ChEMBL
LigandPNGBDBM50470628(CHEMBL336896)copy SMILEScopy InChI
Affinity DataKi:  4.37E+3nMAssay Description:Competition with 20 pM [125I]BH-CCK-8S at Cholecystokinin type A receptor binding sites on guinea pig pancreatic cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930WWVPubMed