BDBM50353214 CHEMBL1829610

SMILES O=C(CNC(=O)c1ccccc1)NC1CN(C1)[C@H]1CC[C@@H](CC1)c1ccc2OCOc2c1

InChI Key InChIKey=VLGQQGBAZGCDNJ-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 = 50353214   

TargetC-C chemokine receptor type 2(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandPNGBDBM50353214(CHEMBL1829610)
Affinity DataIC50: 390nMAssay Description:Displacement of [125I]-MCP1 from CCR2 in human THP1 cells after 2 hrs by microplate scintillation and luminescence countingMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2012
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandPNGBDBM50353214(CHEMBL1829610)
Affinity DataIC50: 2.80E+3nMAssay Description:Displacement of [3H]astemizole from human ERG expressed in HEK293 cells after 1 hrMore data for this Ligand-Target Pair
In Depth
Date in BDB:
3/24/2012
Entry Details Article
PubMed