BDBM50408818 CHEMBL5287134

SMILES N[C@H](CCCNC(N)=N)C(=O)N[C@@H](CCCNC(N)=N)C(=O)NCCC(=O)NC1(CCCCCC1)C(=O)NCCC(=O)N[C@@H](CO)C(=O)N1Cc2ccccc2C[C@@H]1C(=O)N1[C@H]2CCCC[C@H]2C[C@H]1C(O)=O

InChI Key InChIKey=PYVHLAHQEKFLJK-FCAVIIGPSA-N

Data  3 KI  2 EC50

  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 5 hits for monomerid = 50408818   

TargetKappa-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50408818(CHEMBL5287134)
Affinity DataKi:  42nMAssay Description:Antagonist activity at wild type guinea pig NK3 receptor A1142.58T mutant expressed in HEK293 cells assessed as inhibition of [MePhe7]NKB-induced acc...More data for this Ligand-Target Pair
In DepthDetails PubMed
TargetMu-type opioid receptor(MOUSE)TBA
LigandPNGBDBM50408818(CHEMBL5287134)
Affinity DataKi:  54nMAssay Description:Antagonist activity at histamine H3 receptor in guinea pig jejunum assessed as electrically evoked contractionsMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetDelta-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50408818(CHEMBL5287134)
Affinity DataKi:  3.57E+3nMAssay Description:Antagonist activity at P2X7 receptor in human THP1 cells assessed as inhibition of BzATP-induced ethidium uptakeMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50408818(CHEMBL5287134)
Affinity DataEC50:  500nMAssay Description:Antagonist activity at rat H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after 6 hrsMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetMu-type opioid receptor(Homo sapiens (Human))TBA
LigandPNGBDBM50408818(CHEMBL5287134)
Affinity DataEC50:  110nMAssay Description:Inhibition of human recombinant triosephosphate isomerase after 2 hrsMore data for this Ligand-Target Pair
In DepthDetails PubMed