BDBM50416604 CHEMBL1222604

SMILES CC(C)N1[C@@H](CCC1=O)C(=O)NCc1ccc(F)cc1Cl

InChI Key InChIKey=JBPACZXKPFNNDS-UHFFFAOYSA-N

Data  4 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 = 50416604   

TargetP2X purinoceptor 7(Rat)
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50416604(CHEMBL1222604)
Affinity DataIC50: 1.58E+3nMAssay Description:Inhibition of rat P2X7 receptor by ethidium bromide release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/22/2013
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50416604(CHEMBL1222604)
Affinity DataIC50: 316nMAssay Description:Inhibition of human P2X7 receptor by ethidium bromide release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/22/2013
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Human)
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50416604(CHEMBL1222604)
Affinity DataIC50: 100nMAssay Description:Inhibition of human P2X7 receptor by ethidium bromide release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/22/2013
Entry Details Article
PubMed
TargetP2X purinoceptor 7(Rat)
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50416604(CHEMBL1222604)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of rat P2X7 receptor by ethidium bromide release assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/22/2013
Entry Details Article
PubMed