BDBM50397482 CHEMBL2171013

SMILES CN(C(=O)N1CCC(CC1)N1CCC(CC1)Oc1ccc(Cl)c(Cl)c1)S(=O)(=O)c1ccc(C)cc1

InChI Key InChIKey=LPHIWCBAJGQIIF-UHFFFAOYSA-N

Data  2 KI  1 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 3 hits for monomerid = 50397482   

LigandPNGBDBM50397482(CHEMBL2171013)
Affinity DataIC50: 316nMAssay Description:Inhibition of human ERG expressed in CHO cells by IonworksHT assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetHistamine H1 receptor(Human)
Astrazeneca

Curated by ChEMBL
LigandPNGBDBM50397482(CHEMBL2171013)
Affinity DataKi:  2.51nMAssay Description:Displacement of [3H]pyrilamine from human H1 receptor expressed in CHOK1 cellsMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed
TargetC-C chemokine receptor type 3(Human)
Astrazeneca

Curated by ChEMBL
LigandPNGBDBM50397482(CHEMBL2171013)
Affinity DataKi:  100nMAssay Description:Binding affinity to human CCR3 receptor expressed in CHOK1 cells by radioligand displacement assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
5/17/2013
Entry Details Article
PubMed