BDBM50314296 1-(4-chlorophenyl)-1-(1-ethylpiperidin-4-yl)-3-(4-fluorobenzyl)urea::CHEMBL1092105

SMILES CCN1CCC(CC1)N(C(=O)NCc1ccc(F)cc1)c1ccc(Cl)cc1

InChI Key InChIKey=AJQVFVAJQHQUGW-UHFFFAOYSA-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 = 50314296   

TargetHistamine H3 receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50314296(1-(4-chlorophenyl)-1-(1-ethylpiperidin-4-yl)-3-(4-...)
Affinity DataKi:  7nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50314296(1-(4-chlorophenyl)-1-(1-ethylpiperidin-4-yl)-3-(4-...)
Affinity DataKi:  7nMAssay Description:Displacement of [125I]Iodoproxyfan from human recombinant histamine H3 receptor by Competitive binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Bioprojet-Biotech

Curated by ChEMBL
LigandPNGBDBM50314296(1-(4-chlorophenyl)-1-(1-ethylpiperidin-4-yl)-3-(4-...)
Affinity DataIC50:  6.65E+3nMAssay Description:Displacement of [3H]dofetilide from human recombinant ERG by Competitive binding assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPotassium voltage-gated channel subfamily H member 2(Homo sapiens (Human))
Bioprojet-Biotech

Curated by ChEMBL
LigandPNGBDBM50314296(1-(4-chlorophenyl)-1-(1-ethylpiperidin-4-yl)-3-(4-...)
Affinity DataIC50:  6.65E+3nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed