BDBM50406495 CHEMBL2079547

SMILES CSCC[C@H](NC(=O)[C@@H](Cc1ccc(cc1)-c1nnn[nH]1)NC(C)=O)C(=O)NCC(=O)N[C@@H](Cc1c[nH]c2ccccc12)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](Cc1ccccc1)C(N)=O

InChI Key InChIKey=ILOSQOBMIQVKSA-UHFFFAOYSA-N

Data  2 IC50

  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 = 50406495   

TargetCholecystokinin receptor type A(Rat)
Roche Research Center

Curated by ChEMBL
LigandPNGBDBM50406495(CHEMBL2079547)
Affinity DataIC50: 120nMAssay Description:Inhibition of [3H]propanoyl binding to cholecystokinin type A receptor was determined in fresh rat pancreatic tissue membranesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetGastrin/cholecystokinin type B receptor(Bovine)
Roche Research Center

Curated by ChEMBL
LigandPNGBDBM50406495(CHEMBL2079547)
Affinity DataIC50: 76nMAssay Description:Inhibition of [3H]-propanoyl binding to cholecystokinin type B receptor subtype was determined in bovine striatum membranesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed