null

SMILES CCCC[C@H](N(C)C(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CC(=O)OC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc1ccccc1)C(N)=O

InChI Key InChIKey=ZLRHNAHQIXSPTR-LJWNLINESA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50092389   

TargetGastrin/cholecystokinin type B receptor(Homo sapiens (Human))
INSERM

Curated by ChEMBL
LigandPNGBDBM50092389(CHEMBL321456 | N-(1-Carbamoyl-2-phenyl-ethyl)-3-(2...)copy SMILEScopy InChI
Affinity DataKi:  3.61nMAssay Description:Binding affinity against cholecystokinin type B receptor on guinea pig cortex.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2RN373CPubMed
LigandPNGBDBM50092389(CHEMBL321456 | N-(1-Carbamoyl-2-phenyl-ethyl)-3-(2...)copy SMILEScopy InChI
Affinity DataEC50:  2nMAssay Description:Affinity against Cholecystokinin type B receptor expressed in CHO cells on rat brain.More data for this Ligand-Target Pair
In DepthDetails
BindingDB Entry DOI: 10.7270/Q2RN373CPubMed