BDBM50018638 12-[2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-2-(4-nitro-benzyl)-3,7,13-trioxo-1,4,8triaza-cyclotridecane-5-carboxylic acid amide::CHEMBL303418

SMILES N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H]1CCCNC(=O)C[C@H](NC(=O)[C@H](Cc2ccc(cc2)[N+]([O-])=O)NC1=O)C(N)=O

InChI Key InChIKey=YHLQBUMFTKANHO-LRSLUSHPSA-N

Data  2 KI  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 4 hits for monomerid = 50018638   

TargetMu-type opioid receptor(Rattus norvegicus (rat))
Clinical Research Institute Of Montreal

Curated by ChEMBL
LigandPNGBDBM50018638(12-[2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-2...)
Affinity DataKi:  273nMAssay Description:Binding affinity towards Opioid receptor mu 1 in rat brain membrane using [3H]-DAGO as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
Clinical Research Institute Of Montreal

Curated by ChEMBL
LigandPNGBDBM50018638(12-[2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-2...)
Affinity DataKi:  5.06E+3nMAssay Description:Inhibition of [3H]-DSLET binding to rat brain membrane Opioid receptor delta 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(GUINEA PIG)
Clinical Research Institute Of Montreal

Curated by ChEMBL
LigandPNGBDBM50018638(12-[2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-2...)
Affinity DataIC50:  2.34E+3nMAssay Description:Inhibitory activity towards electrically induced contractions in guinea pig ileum expressing Opioid receptor mu 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(MOUSE)
Clinical Research Institute Of Montreal

Curated by ChEMBL
LigandPNGBDBM50018638(12-[2-Amino-3-(4-hydroxy-phenyl)-propionylamino]-2...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibitory activity towards electrically induced contractions in mouse vas deferens expressing delta opioid receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed