Compile Data Set for Download or QSAR
Report error Found 41 Enz. Inhib. hit(s) with all data for entry = 50031500
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314290BDBM50314290(3-benzyl-1-(4-bromophenyl)-1-(1-(pyridin-4-ylmethy...)
Affinity DataKi:  2nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314288BDBM50314288(1-(1-((2-aminopyridin-4-yl)methyl)piperidin-4-yl)-...)
Affinity DataKi:  3nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314296BDBM50314296(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 Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314294BDBM50314294(1-(4-bromophenyl)-1-(1-cyclopentylpiperidin-4-yl)-...)
Affinity DataKi:  7nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314291BDBM50314291(3-benzyl-1-(4-bromophenyl)-1-(1-(pyridazin-4-ylmet...)
Affinity DataKi:  10nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314292BDBM50314292(3-benzyl-1-(4-bromophenyl)-1-(1-cyclopentylpiperid...)
Affinity DataKi:  10nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314293BDBM50314293(1-(4-bromophenyl)-1-(1-cyclopentylpiperidin-4-yl)-...)
Affinity DataKi:  14nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314311BDBM50314311(1-(4-chlorophenyl)-3-(4-fluorobenzyl)-1-(1-(pyridi...)
Affinity DataKi:  16nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314295BDBM50314295(1-(4-bromophenyl)-3-(3,4-dichlorobenzyl)-1-(1-ethy...)
Affinity DataKi:  23nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314313BDBM50314313(1-(4-bromophenyl)-1-(1-cyclopentylpiperidin-4-yl)-...)
Affinity DataKi:  36nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314297BDBM50314297(1-(5-chloropyridin-2-yl)-1-(1-ethylpiperidin-4-yl)...)
Affinity DataKi:  41nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314315BDBM50314315(1-(4-bromophenyl)-1-(1-cyclopentylpiperidin-4-yl)-...)
Affinity DataKi:  47nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314289BDBM50314289(1-(4-chlorophenyl)-3-(4-fluorobenzyl)-1-(1-(pyrida...)
Affinity DataKi:  49nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314313BDBM50314313(1-(4-bromophenyl)-1-(1-cyclopentylpiperidin-4-yl)-...)
Affinity DataIC50: 61nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314307BDBM50314307(1-(4-bromophenyl)-3-(4-fluorobenzyl)-1-(1-(2-hydro...)
Affinity DataKi:  67nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314306BDBM50314306(1-(4-chlorophenyl)-3-(4-fluorobenzyl)-1-(1-(2-hydr...)
Affinity DataKi:  86nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314292BDBM50314292(3-benzyl-1-(4-bromophenyl)-1-(1-cyclopentylpiperid...)
Affinity DataIC50: 178nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314293BDBM50314293(1-(4-bromophenyl)-1-(1-cyclopentylpiperidin-4-yl)-...)
Affinity DataIC50: 188nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314314BDBM50314314(1-(4-bromophenyl)-1-(1-cyclopentylpiperidin-4-yl)-...)
Affinity DataKi:  191nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314294BDBM50314294(1-(4-bromophenyl)-1-(1-cyclopentylpiperidin-4-yl)-...)
Affinity DataIC50: 202nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314288BDBM50314288(1-(1-((2-aminopyridin-4-yl)methyl)piperidin-4-yl)-...)
Affinity DataIC50: 384nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314298BDBM50314298(1-(1-ethylpiperidin-4-yl)-3-(4-fluorobenzyl)-1-(4-...)
Affinity DataKi:  447nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314300BDBM50314300(1-(1-ethylpiperidin-4-yl)-3-(4-fluorobenzyl)-1-(4-...)
Affinity DataKi:  560nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314312BDBM50314312(1-(4-chlorophenyl)-3-(4-fluorobenzyl)-1-(1-((2-hyd...)
Affinity DataKi:  624nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314305BDBM50314305(1-(4-chlorophenyl)-3-(4-fluorobenzyl)-1-(1-(methyl...)
Affinity DataKi:  858nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314302BDBM50314302(1-(1-ethylpiperidin-4-yl)-3-(4-fluorobenzyl)-1-(pi...)
Affinity DataKi: >1.00E+3nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314301BDBM50314301(1-(4-bromobenzyl)-1-(1-ethylpiperidin-4-yl)-3-(4-f...)
Affinity DataKi: >1.00E+3nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314299BDBM50314299(1-(1-cyclopentylpiperidin-4-yl)-3-(4-fluorobenzyl)...)
Affinity DataKi: >1.00E+3nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314304BDBM50314304(1-(4-chlorophenyl)-3-(4-fluorobenzyl)-1-(piperidin...)
Affinity DataKi: >1.00E+3nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314303BDBM50314303(1-(1-ethylpiperidin-4-yl)-3-(4-fluorobenzyl)-1-(1-...)
Affinity DataKi: >1.00E+3nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314308BDBM50314308(1-(4-chlorophenyl)-1-(1-(2,3-dihydroxypropyl)piper...)
Affinity DataKi: >1.00E+3nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314310BDBM50314310(1-(4-chlorophenyl)-3-(4-fluorobenzyl)-1-(1-(pyridi...)
Affinity DataKi: >1.00E+3nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314309BDBM50314309(4-(1-(4-chlorophenyl)-3-(4-fluorobenzyl)ureido)-N-...)
Affinity DataKi: >1.00E+3nMAssay Description:Antagonist activity at human recombinant histamine 3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314290BDBM50314290(3-benzyl-1-(4-bromophenyl)-1-(1-(pyridin-4-ylmethy...)
Affinity DataIC50: 2.31E+3nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314311BDBM50314311(1-(4-chlorophenyl)-3-(4-fluorobenzyl)-1-(1-(pyridi...)
Affinity DataIC50: 3.81E+3nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314296BDBM50314296(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 Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314307BDBM50314307(1-(4-bromophenyl)-3-(4-fluorobenzyl)-1-(1-(2-hydro...)
Affinity DataIC50: 7.88E+3nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314297BDBM50314297(1-(5-chloropyridin-2-yl)-1-(1-ethylpiperidin-4-yl)...)
Affinity DataIC50: 9.19E+3nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314289BDBM50314289(1-(4-chlorophenyl)-3-(4-fluorobenzyl)-1-(1-(pyrida...)
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314306BDBM50314306(1-(4-chlorophenyl)-3-(4-fluorobenzyl)-1-(1-(2-hydr...)
Affinity DataIC50: 1.27E+4nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed
TargetPotassium voltage-gated channel subfamily H member 2(Human)
Merck Research Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50314291BDBM50314291(3-benzyl-1-(4-bromophenyl)-1-(1-(pyridazin-4-ylmet...)
Affinity DataIC50: 1.38E+4nMAssay Description:Inhibition of human ERG by ion works assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/18/2010
Entry Details Article
PubMed