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Found 184 with Last Name = 'phillips' and Initial = 'jg'
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM50074629(4-[(1R,2R)-2-(5,5-Dimethyl-hex-1-ynyl)-cyclopropyl...)
Affinity DataKi:  0.120nMAssay Description:Binding affinity at histamine H3 receptor in rat cortical membranes by [3H]-Nalpha-methylhistamine displacement.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM22541(Clobenpropit | N''-[(4-chlorophenyl)methyl]{[3-(1H...)
Affinity DataKi:  0.180nMAssay Description:Histamine H3 receptor affinity of compound was determined in rat cortical membranes using the H3 selective agonist ligand, [3H]N-alpha-methylhistamin...More data for this Ligand-Target Pair
In DepthDetails Article
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM22541(Clobenpropit | N''-[(4-chlorophenyl)methyl]{[3-(1H...)
Affinity DataKi:  0.180nMAssay Description:Inhibition of [3H]- N-alpha-methylhistamine from histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM22916(5-{3-[(4-iodophenyl)methoxy]propyl}-1H-imidazole |...)
Affinity DataKi:  0.300nMAssay Description:Histamine H3 receptor affinity of compound was determined in rat cortical membranes using the H3 selective agonist ligand, [3H]N-alpha-methylhistamin...More data for this Ligand-Target Pair
In DepthDetails Article
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM50074627(4-[2-(5,5-Dimethyl-hex-1-ynyl)-cyclopropyl]-1H-imi...)
Affinity DataKi:  0.330nMAssay Description:Binding affinity at histamine H3 receptor in rat cortical membranes by [3H]-Nalpha-methylhistamine displacement.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM50070217(3-(3-Bromo-4-methoxy-phenyl)-2-[(E)-hydroxyimino]-...)
Affinity DataKi:  0.5nMAssay Description:Inhibition of [3H]- N-alpha-methylhistamine from histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038757(6-Bromo-3-((R)-2-pyridin-3-yl-thiazolidine-4-carbo...)
Affinity DataKi:  0.600nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038809(3-((R)-2-Pyridin-3-yl-thiazolidine-4-carbonyl)-ind...)
Affinity DataKi:  0.800nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM50070214(4-(7,7-Dimethyl-oct-3-ynyl)-1H-imidazole | CHEMBL2...)
Affinity DataKi:  0.800nMAssay Description:Binding affinity at histamine H3 receptor in rat cortical membranes by [3H]-Nalpha-methylhistamine displacement.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM50070214(4-(7,7-Dimethyl-oct-3-ynyl)-1H-imidazole | CHEMBL2...)
Affinity DataKi:  0.800nMAssay Description:Inhibition of [3H]- N-alpha-methylhistamine from histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHrh3 protein(RAT)
Gliatech

Curated by PDSP Ki Database
LigandPNGBDBM50070214(4-(7,7-Dimethyl-oct-3-ynyl)-1H-imidazole | CHEMBL2...)
Affinity DataKi:  0.830nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM50070220(4-(6-Cyclopentyl-hex-3-ynyl)-1H-imidazole | CHEMBL...)
Affinity DataKi:  0.900nMAssay Description:Binding affinity at histamine H3 receptor in rat cortical membranes by [3H]-Nalpha-methylhistamine displacement.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHrh3 protein(RAT)
Gliatech

Curated by PDSP Ki Database
LigandPNGBDBM50070220(4-(6-Cyclopentyl-hex-3-ynyl)-1H-imidazole | CHEMBL...)
Affinity DataKi:  0.950nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM50070220(4-(6-Cyclopentyl-hex-3-ynyl)-1H-imidazole | CHEMBL...)
Affinity DataKi:  0.950nMAssay Description:Inhibition of [3H]- N-alpha-methylhistamine from histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038806(6-Chloro-3-((R)-2-pyridin-3-yl-thiazolidine-4-carb...)
Affinity DataKi:  1nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM7967(1-methyl-5-(beta-aminoethyl)-imidazole | 2-(1-meth...)
Affinity DataKi:  1nMAssay Description:Inhibition of [3H]- N-alpha-methylhistamine from histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038834(6-Benzoyl-3-((R)-2-pyridin-3-yl-thiazolidine-4-car...)
Affinity DataKi:  1nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038792(6-Benzyloxy-3-((R)-2-pyridin-3-yl-thiazolidine-4-c...)
Affinity DataKi:  1nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038750(3-((R)-2-Pyridin-3-yl-thiazolidine-4-carbonyl)-ind...)
Affinity DataKi:  1nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHrh3 protein(RAT)
Gliatech

Curated by PDSP Ki Database
LigandPNGBDBM85407(GT 2231)
In DepthDetails PubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038777((7-Benzyloxy-1H-indol-3-yl)-((R)-2-pyridin-3-yl-th...)
Affinity DataKi:  1.10nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038780(CHEMBL64428 | [3-((R)-2-Pyridin-3-yl-thiazolidine-...)
Affinity DataKi:  1.20nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038786(6-Phenylethynyl-3-((R)-2-pyridin-3-yl-thiazolidine...)
Affinity DataKi:  1.30nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038825(6-Benzyloxy-3-((R)-2-pyridin-3-yl-thiazolidine-4-c...)
Affinity DataKi:  1.40nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038810(3-((R)-2-Pyridin-3-yl-thiazolidine-4-carbonyl)-ind...)
Affinity DataKi:  1.40nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM50074630(4-[2-(4-Cyclopentyl-but-1-ynyl)-cyclopropyl]-1H-im...)
Affinity DataKi:  1.43nMAssay Description:Binding affinity at histamine H3 receptor in rat cortical membranes by [3H]-Nalpha-methylhistamine displacement.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038819(CHEMBL64464 | Morpholin-4-yl-[3-((R)-2-pyridin-3-y...)
Affinity DataKi:  1.5nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM22914(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Affinity DataKi:  1.5nMAssay Description:Antagonistic activity of the compound was evaluated against histamine H3 receptor using [3H]- N-alpha-methylhistamine as radioligand in experiment 2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038759((6-Benzyloxy-1H-indol-3-yl)-((R)-2-pyridin-3-yl-th...)
Affinity DataKi:  1.60nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038749((R)-2-Pyridin-3-yl-thiazolidine-4-carboxylic acid ...)
Affinity DataKi:  1.60nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038801(CHEMBL62830 | [6-(4-Fluoro-benzyloxy)-1H-indol-3-y...)
Affinity DataKi:  1.60nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM50074624(4-[2-(4-Cyclohexyl-but-1-ynyl)-cyclopropyl]-1H-imi...)
Affinity DataKi:  1.80nMAssay Description:Binding affinity at histamine H3 receptor in rat cortical membranes by [3H]-Nalpha-methylhistamine displacement.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038835(6-(4-Fluoro-benzyloxy)-3-((R)-2-pyridin-3-yl-thiaz...)
Affinity DataKi:  1.80nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHrh3 protein(RAT)
Gliatech

Curated by PDSP Ki Database
LigandPNGBDBM22914(CHEMBL260374 | N-cyclohexyl-4-(1H-imidazol-5-yl)pi...)
Affinity DataKi:  1.80nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038752(CHEMBL64636 | [6-(4-Fluoro-phenoxy)-1H-indol-3-yl]...)
Affinity DataKi:  1.90nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038760(6-Fluoro-3-((R)-2-pyridin-3-yl-thiazolidine-4-carb...)
Affinity DataKi:  1.90nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038788(3-((R)-2-Pyridin-3-yl-thiazolidine-4-carbonyl)-ind...)
Affinity DataKi:  2nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038754(6-(4-Fluoro-phenoxy)-3-((R)-2-pyridin-3-yl-thiazol...)
Affinity DataKi:  2.20nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038763(CHEMBL293259 | N-Methyl-2-[3-((R)-2-pyridin-3-yl-t...)
Affinity DataKi:  2.40nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038830(6-Methyl-3-((R)-2-pyridin-3-yl-thiazolidine-4-carb...)
Affinity DataKi:  2.60nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM50074628(4-Undec-3-ynyl-1H-imidazole | CHEMBL170723)
Affinity DataKi:  2.80nMAssay Description:Binding affinity at histamine H3 receptor in rat cortical membranes by [3H]-Nalpha-methylhistamine displacement.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM50070211(4-(6-Cyclohexyl-hex-3-ynyl)-1H-imidazole | CHEMBL1...)
Affinity DataKi:  2.90nMAssay Description:Binding affinity at histamine H3 receptor in rat cortical membranes by [3H]-Nalpha-methylhistamine displacement.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHrh3 protein(RAT)
Gliatech

Curated by PDSP Ki Database
LigandPNGBDBM50070211(4-(6-Cyclohexyl-hex-3-ynyl)-1H-imidazole | CHEMBL1...)
Affinity DataKi:  2.90nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
Gliatech

Curated by ChEMBL
LigandPNGBDBM50070211(4-(6-Cyclohexyl-hex-3-ynyl)-1H-imidazole | CHEMBL1...)
Affinity DataKi:  2.90nMAssay Description:Inhibition of [3H]- N-alpha-methylhistamine from histamine H3 receptorMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038808(6-(2-Methoxy-ethoxy)-3-((R)-2-pyridin-3-yl-thiazol...)
Affinity DataKi:  3nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038769(3-((R)-2-Pyridin-3-yl-thiazolidine-4-carbonyl)-ind...)
Affinity DataKi:  3nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Homo sapiens (Human))
Gliatech

Curated by PDSP Ki Database
LigandPNGBDBM85405(GT 2227 | GT 2228)
Affinity DataKi:  3.20nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038826((1H-Indol-3-yl)-((R)-2-pyridin-3-yl-thiazolidin-4-...)
Affinity DataKi:  3.40nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlatelet-activating factor receptor(Cavia porcellus)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50038776((4-Chloro-phenyl)-[3-((R)-2-pyridin-3-yl-thiazolid...)
Affinity DataKi:  3.40nMAssay Description:Antagonist activity against platelet activating factor (PAF) receptor in rabbit platelet membranes using [3H]C18-PAF as radioligandMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHrh3 protein(RAT)
Gliatech

Curated by PDSP Ki Database
LigandPNGBDBM85412(GT 2287)
Affinity DataKi:  3.40nMMore data for this Ligand-Target Pair
In DepthDetails PubMed
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