Compile Data Set for Download or QSAR
Report error Found 18 Enz. Inhib. hit(s) with all data for entry = 50014834
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 22914BDBM22914(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Affinity DataKi:  4nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148122BDBM50148122(4-[3-(3-Trifluoromethyl-phenoxy)-propyl]-1H-imidaz...)
Affinity DataKi:  8.40nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148120BDBM50148120(4-[3-(3-Nitro-phenoxy)-propyl]-1H-imidazole | CHEM...)
Affinity DataKi:  9.40nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50053278BDBM50053278(4-[3-(1H-Imidazol-4-yl)-propoxy]-benzonitrile | 4-...)
Affinity DataKi:  12nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50053298BDBM50053298(4-[3-(4-Trifluoromethyl-phenoxy)-propyl]-1H-imidaz...)
Affinity DataKi:  14nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148121BDBM50148121(4-[3-(3-Ethyl-phenoxy)-propyl]-1H-imidazole | CHEM...)
Affinity DataKi:  15nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148116BDBM50148116(4-[2-(3-Trifluoromethyl-phenoxy)-ethyl]-1H-imidazo...)
Affinity DataKi:  18nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148117BDBM50148117(4-[3-(3-Bromo-phenoxy)-propyl]-1H-imidazole | CHEM...)
Affinity DataKi:  19nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50409931BDBM50409931(CHEMBL2112499)
Affinity DataKi:  20nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148125BDBM50148125(4-[3-(3-tert-Butyl-phenoxy)-propyl]-1H-imidazole |...)
Affinity DataKi:  22nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148114BDBM50148114(4-[2-(3-Trifluoromethyl-phenylsulfanyl)-ethyl]-1H-...)
Affinity DataKi:  23nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148124BDBM50148124(4-[3-(3-Isopropyl-phenoxy)-propyl]-1H-imidazole | ...)
Affinity DataKi:  29nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148115BDBM50148115(4-(3-m-Tolyloxy-propyl)-1H-imidazole | CHEMBL11041...)
Affinity DataKi:  37nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148118BDBM50148118(4-[4-(3-Trifluoromethyl-phenyl)-butyl]-1H-imidazol...)
Affinity DataKi:  38nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148113BDBM50148113(4-[3-(3-Trifluoromethyl-phenylsulfanyl)-propyl]-1H...)
Affinity DataKi:  38nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50092833BDBM50092833(CHEMBL128923 | CHEMBL112951 | 4-(3-Phenoxy-propyl)...)
Affinity DataKi:  55nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148119BDBM50148119(3-[3-(1H-Imidazol-4-yl)-propoxy]-benzonitrile | CH...)
Affinity DataKi:  108nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
University College London

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50148123BDBM50148123(4-[3-(3,5-Bis-trifluoromethyl-phenoxy)-propyl]-1H-...)
Affinity DataKi:  116nMAssay Description:In vitro inhibitory activity against histamine H3 receptor using [3H]histamine as radioligand from rat cerebral cortex synaptosomesMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed