Compile Data Set for Download or QSAR
Report error Found 60 Enz. Inhib. hit(s) with all data for entry = 50016874
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174619BDBM50174619({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.0500nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174627BDBM50174627({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.0800nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174621BDBM50174621({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.110nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174619BDBM50174619({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.110nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174613BDBM50174613(4-({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-ben...)
Affinity DataKi:  0.130nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174637BDBM50174637({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.140nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174615BDBM50174615({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.190nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174620BDBM50174620({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.220nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174614BDBM50174614(4-{2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benz...)
Affinity DataKi:  0.270nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174627BDBM50174627({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.270nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174634BDBM50174634(3-{2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benz...)
Affinity DataKi:  0.290nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174624BDBM50174624({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.290nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174631BDBM50174631({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.300nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174629BDBM50174629({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.310nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174636BDBM50174636({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.310nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174623BDBM50174623((6-Chloro-pyridazin-3-yl)-{2-[2-((R)-2-methyl-pyrr...)
Affinity DataKi:  0.310nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174625BDBM50174625((5-Ethyl-pyrimidin-2-yl)-{2-[2-((R)-2-methyl-pyrro...)
Affinity DataKi:  0.330nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174639BDBM50174639(6-({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-ben...)
Affinity DataKi:  0.340nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174637BDBM50174637({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.350nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174621BDBM50174621({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.380nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174612BDBM50174612(3-({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-ben...)
Affinity DataKi:  0.400nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174613BDBM50174613(4-({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-ben...)
Affinity DataKi:  0.400nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174640BDBM50174640({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.430nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50139391BDBM50139391((R)-4-(2-(2-(2-methylpyrrolidin-1-yl)ethyl)benzofu...)
Affinity DataKi:  0.450nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174616BDBM50174616({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.540nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174625BDBM50174625((5-Ethyl-pyrimidin-2-yl)-{2-[2-((R)-2-methyl-pyrro...)
Affinity DataKi:  0.580nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174632BDBM50174632((5-Ethyl-pyrimidin-2-yl)-{2-[2-((R)-2-methyl-pyrro...)
Affinity DataKi:  0.620nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174615BDBM50174615({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.680nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174617BDBM50174617({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.690nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174633BDBM50174633((3,5-Dinitro-pyridin-2-yl)-{2-[2-((R)-2-methyl-pyr...)
Affinity DataKi:  0.710nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174635BDBM50174635(2,2,2-Trifluoro-1-[4-({2-[2-((R)-2-methyl-pyrrolid...)
Affinity DataKi:  0.740nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174638BDBM50174638({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.740nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174628BDBM50174628(2-({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-ben...)
Affinity DataKi:  0.740nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174624BDBM50174624({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.800nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174626BDBM50174626({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.840nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174629BDBM50174629({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.870nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174620BDBM50174620({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  0.870nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174622BDBM50174622(3-({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-ben...)
Affinity DataKi:  1.04nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174612BDBM50174612(3-({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-ben...)
Affinity DataKi:  1.18nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174631BDBM50174631({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  1.19nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Human)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174630BDBM50174630((5-Bromo-pyrimidin-2-yl)-{2-[2-((R)-2-methyl-pyrro...)
Affinity DataKi:  1.22nMAssay Description:In vitro binding affinity for human histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50139391BDBM50139391((R)-4-(2-(2-(2-methylpyrrolidin-1-yl)ethyl)benzofu...)
Affinity DataKi:  1.23nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174614BDBM50174614(4-{2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benz...)
Affinity DataKi:  1.35nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174639BDBM50174639(6-({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-ben...)
Affinity DataKi:  1.42nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174634BDBM50174634(3-{2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benz...)
Affinity DataKi:  1.47nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174623BDBM50174623((6-Chloro-pyridazin-3-yl)-{2-[2-((R)-2-methyl-pyrr...)
Affinity DataKi:  1.58nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174628BDBM50174628(2-({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-ben...)
Affinity DataKi:  1.92nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174636BDBM50174636({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  2.01nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174638BDBM50174638({2-[2-((R)-2-Methyl-pyrrolidin-1-yl)-ethyl]-benzof...)
Affinity DataKi:  2.12nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetHistamine H3 receptor(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50174635BDBM50174635(2,2,2-Trifluoro-1-[4-({2-[2-((R)-2-methyl-pyrrolid...)
Affinity DataKi:  2.36nMAssay Description:In vitro binding affinity for rat histamine H3 receptor using [3H]N-alpha-methylhistamineMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
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