Compile Data Set for Download or QSAR
Report error Found 64 Enz. Inhib. hit(s) with all data for entry = 50018304
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194208BDBM50194208((1S,2R)-trans-2-[2-(4-chlorobenzylamino)ethyl]-1-(...)
Affinity DataKi:  3.60nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194202BDBM50194202((1S,2R)-trans-2-[2-(cyclohexylmethylamino)ethyl]-1...)
Affinity DataKi:  5.30nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194205BDBM50194205((1R,2S)-trans-2-[2-(4-chlorobenzylamino)ethyl]-1-(...)
Affinity DataKi:  7.60nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194205BDBM50194205((1R,2S)-trans-2-[2-(4-chlorobenzylamino)ethyl]-1-(...)
Affinity DataKi:  8.40nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194208BDBM50194208((1S,2R)-trans-2-[2-(4-chlorobenzylamino)ethyl]-1-(...)
Affinity DataIC50: 8.5nMAssay Description:Antagonist activity at human H3 receptor expressed in 293-EBNA cells assessed as inhibition of histamine agonist activity by luciferase reporter gene...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194203BDBM50194203((1R,2R)-cis-2-[2-(4-chlorobenzylamino)ethyl]-1-(1H...)
Affinity DataKi:  13.9nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 22914BDBM22914(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Affinity DataIC50: 16nMAssay Description:Antagonist activity at human H3 receptor expressed in 293-EBNA cells assessed as inhibition of histamine agonist activity by luciferase reporter gene...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194205BDBM50194205((1R,2S)-trans-2-[2-(4-chlorobenzylamino)ethyl]-1-(...)
Affinity DataIC50: 17nMAssay Description:Antagonist activity at human H3 receptor expressed in 293-EBNA cells assessed as inhibition of histamine agonist activity by luciferase reporter gene...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194211BDBM50194211((1S,2S)-cis-2-[2-(cyclohexylmethylamino)ethyl]-1-(...)
Affinity DataKi:  20.5nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194206BDBM50194206((1R,2S)-trans-2-[2-(cyclohexylmethylamino)ethyl]-1...)
Affinity DataKi:  31.2nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194209BDBM50194209((1R,2R)-trans-2-(cyclohexylmethylamino)methyl-1-(1...)
Affinity DataKi:  34.4nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194206BDBM50194206((1R,2S)-trans-2-[2-(cyclohexylmethylamino)ethyl]-1...)
Affinity DataKi:  35nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194202BDBM50194202((1S,2R)-trans-2-[2-(cyclohexylmethylamino)ethyl]-1...)
Affinity DataIC50: 37nMAssay Description:Antagonist activity at human H3 receptor expressed in 293-EBNA cells assessed as inhibition of histamine agonist activity by luciferase reporter gene...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194208BDBM50194208((1S,2R)-trans-2-[2-(4-chlorobenzylamino)ethyl]-1-(...)
Affinity DataKi:  37.2nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194212BDBM50194212((1S,2S)-cis-2-[2-(4-chlorobenzylamino)ethyl]-1-(1H...)
Affinity DataKi:  43.7nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H1 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 7966BDBM7966([3H]histamine | 2-(1H-imidazol-4-yl)ethan-1-amine ...)
Affinity DataEC50:  45nMAssay Description:Agonist activity at human H1 receptor expressed in 293-EBNA cells by luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 22914BDBM22914(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Affinity DataKi:  51.1nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 7966BDBM7966([3H]histamine | 2-(1H-imidazol-4-yl)ethan-1-amine ...)
Affinity DataEC50:  88nMAssay Description:Agonist activity at human H3 receptor expressed in 293-EBNA cells by luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194204BDBM50194204((1S,2R)-cis-2-(4-chlorobenzylamino)methyl-1-(1H-im...)
Affinity DataKi:  88nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194216BDBM50194216((1S,2S)-trans-2-(cyclohexylmethylamino)methyl-1-(1...)
Affinity DataKi:  90.4nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194203BDBM50194203((1R,2R)-cis-2-[2-(4-chlorobenzylamino)ethyl]-1-(1H...)
Affinity DataKi:  103nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194205BDBM50194205((1R,2S)-trans-2-[2-(4-chlorobenzylamino)ethyl]-1-(...)
Affinity DataIC50: 110nMAssay Description:Antagonist activity at human H4 receptor expressed in 293-EBNA cells assessed as inhibition of histamine agonist activity by luciferase reporter gene...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194210BDBM50194210((1S,2S)-trans-2-(4-chlorobenzylamino)methyl-1-(1H-...)
Affinity DataKi:  115nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194207BDBM50194207((1R,2R)-trans-2-(4-chlorobenzylamino)methyl-1-(1H-...)
Affinity DataKi:  118nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 22914BDBM22914(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Affinity DataKi:  124nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194202BDBM50194202((1S,2R)-trans-2-[2-(cyclohexylmethylamino)ethyl]-1...)
Affinity DataKi:  127nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194212BDBM50194212((1S,2S)-cis-2-[2-(4-chlorobenzylamino)ethyl]-1-(1H...)
Affinity DataKi:  130nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194209BDBM50194209((1R,2R)-trans-2-(cyclohexylmethylamino)methyl-1-(1...)
Affinity DataKi:  143nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194211BDBM50194211((1S,2S)-cis-2-[2-(cyclohexylmethylamino)ethyl]-1-(...)
Affinity DataKi:  177nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194210BDBM50194210((1S,2S)-trans-2-(4-chlorobenzylamino)methyl-1-(1H-...)
Affinity DataKi:  203nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194216BDBM50194216((1S,2S)-trans-2-(cyclohexylmethylamino)methyl-1-(1...)
Affinity DataKi:  289nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H2 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 7966BDBM7966([3H]histamine | 2-(1H-imidazol-4-yl)ethan-1-amine ...)
Affinity DataEC50:  650nMAssay Description:Agonist activity at human H2 receptor expressed in 293-EBNA cells by luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 22914BDBM22914(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Affinity DataIC50: 680nMAssay Description:Antagonist activity at human H4 receptor expressed in 293-EBNA cells assessed as inhibition of histamine agonist activity by luciferase reporter gene...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194208BDBM50194208((1S,2R)-trans-2-[2-(4-chlorobenzylamino)ethyl]-1-(...)
Affinity DataIC50: 860nMAssay Description:Antagonist activity at human H4 receptor expressed in 293-EBNA cells assessed as inhibition of histamine agonist activity by luciferase reporter gene...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194213BDBM50194213((1R,2R)-cis-2-[2-(cyclohexylmethylamino)ethyl]-1-(...)
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194215BDBM50194215((1R,2S)-cis-2-(4-chlorobenzylamino)methyl-1-(1H-im...)
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194217BDBM50194217((1S,2R)-cis-2-(cyclohexylmethylamino)methyl-1-(1H-...)
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194204BDBM50194204((1S,2R)-cis-2-(4-chlorobenzylamino)methyl-1-(1H-im...)
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194214BDBM50194214((1R,2S)-cis-2-(cyclohexylmethylamino)methyl-1-(1H-...)
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]histamine form human H4 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194217BDBM50194217((1S,2R)-cis-2-(cyclohexylmethylamino)methyl-1-(1H-...)
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194214BDBM50194214((1R,2S)-cis-2-(cyclohexylmethylamino)methyl-1-(1H-...)
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194207BDBM50194207((1R,2R)-trans-2-(4-chlorobenzylamino)methyl-1-(1H-...)
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194213BDBM50194213((1R,2R)-cis-2-[2-(cyclohexylmethylamino)ethyl]-1-(...)
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194215BDBM50194215((1R,2S)-cis-2-(4-chlorobenzylamino)methyl-1-(1H-im...)
Affinity DataKi: >1.00E+3nMAssay Description:Displacement of [3H]Nalpha-methylhistamine form human H3 receptorMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194202BDBM50194202((1S,2R)-trans-2-[2-(cyclohexylmethylamino)ethyl]-1...)
Affinity DataIC50: 1.50E+3nMAssay Description:Antagonist activity at human H4 receptor expressed in 293-EBNA cells assessed as inhibition of histamine agonist activity by luciferase reporter gene...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 7966BDBM7966([3H]histamine | 2-(1H-imidazol-4-yl)ethan-1-amine ...)
Affinity DataEC50:  1.80E+3nMAssay Description:Agonist activity at human H4 receptor expressed in 293-EBNA cells by luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H1 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194205BDBM50194205((1R,2S)-trans-2-[2-(4-chlorobenzylamino)ethyl]-1-(...)
Affinity DataIC50: 6.80E+3nMAssay Description:Antagonist activity at human H1 receptor expressed in 293-EBNA cells assessed as inhibition of histamine agonist activity by luciferase reporter gene...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H1 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194208BDBM50194208((1S,2R)-trans-2-[2-(4-chlorobenzylamino)ethyl]-1-(...)
Affinity DataIC50: 8.50E+3nMAssay Description:Antagonist activity at human H1 receptor expressed in 293-EBNA cells assessed as inhibition of histamine agonist activity by luciferase reporter gene...More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H4 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194205BDBM50194205((1R,2S)-trans-2-[2-(4-chlorobenzylamino)ethyl]-1-(...)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at human H4 receptor expressed in 293-EBNA cells by luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H1 receptor(Human)
Hokkaido University

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50194208BDBM50194208((1S,2R)-trans-2-[2-(4-chlorobenzylamino)ethyl]-1-(...)
Affinity DataEC50: >1.00E+4nMAssay Description:Agonist activity at human H1 receptor expressed in 293-EBNA cells by luciferase reporter gene assayMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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