Compile Data Set for Download or QSAR
maximum 50k data
Found 13 of kd for UniProtKB: Q9QYN8
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50278350(4-fluoro-1-(4-(3-(piperidin-1-yl)propoxy)benzyl)pi...)
Affinity DataKd:  0.340nMAssay Description:Binding affinity to rat brain histamine H3 receptor after 1 hr by gamma countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50346208((1-isopropylpiperidin-4-yl)(4-(piperidin-1-ylmethy...)
Affinity DataKd:  1.82nMAssay Description:Antagonist activity at histamine H3 receptor in rat cortical hemispheres assessed as inhibition of forskolin stimulated cAMP accumulation after 6 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50321467((4-cyclobutyl-1,4-diazepan-1-yl)(6-(4-fluorophenox...)
Affinity DataKd:  3.55nMAssay Description:Antagonist activity at rat histamine H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50321472((4-cyclobutyl-1,4-diazepan-1-yl)(6-phenoxypyridin-...)
Affinity DataKd:  3.72nMAssay Description:Antagonist activity at rat histamine H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50321464((6-(4-chlorophenoxy)pyridin-3-yl)(4-cyclobutyl-1,4...)
Affinity DataKd:  3.98nMAssay Description:Antagonist activity at rat histamine H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50321468((4-cyclobutyl-1,4-diazepan-1-yl)(6-(3-fluorophenox...)
Affinity DataKd:  4.17nMAssay Description:Antagonist activity at rat histamine H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50321465((6-(3-chlorophenoxy)pyridin-3-yl)(4-cyclobutyl-1,4...)
Affinity DataKd:  5.01nMAssay Description:Antagonist activity at rat histamine H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50346201((4-Isopropyl-piperazin-1-yl)-(6-piperidin-1-ylmeth...)
Affinity DataKd:  6.31nMAssay Description:Antagonist activity at histamine H3 receptor in rat cortical hemispheres assessed as inhibition of forskolin stimulated cAMP accumulation after 6 hrsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50321471((4-cyclobutyl-1,4-diazepan-1-yl)(6-(3,4-dichloroph...)
Affinity DataKd:  6.92nMAssay Description:Antagonist activity at rat histamine H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50321466(3-(5-(4-cyclobutyl-1,4-diazepane-1-carbonyl)pyridi...)
Affinity DataKd:  9.55nMAssay Description:Antagonist activity at rat histamine H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50321470((6-(3-chlorophenoxy)pyridin-3-yl)(4-cyclopropyl-1,...)
Affinity DataKd:  11.5nMAssay Description:Antagonist activity at rat histamine H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50321463((4-cyclobutyl-1,4-diazepan-1-yl)(5-(4-fluorophenox...)
Affinity DataKd:  26.3nMAssay Description:Antagonist activity at rat histamine H3 receptor expressed in human SK-N-MC cells assessed as inhibition of forskolin-induced cAMP accumulation after...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistamine H3 receptor(Rattus norvegicus (rat))
ETH Zurich (Swiss Federal Institute of Technology)

Curated by ChEMBL
LigandPNGBDBM50278350(4-fluoro-1-(4-(3-(piperidin-1-yl)propoxy)benzyl)pi...)
Affinity DataKd: >3.00E+3nMAssay Description:Binding affinity to rat histamine H3 receptor low affinity site after 1 hr by Schard plot analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed