Compile Data Set for Download or QSAR
maximum 50k data
Found 46 Enz. Inhib. hit(s) with all data for entry = 50013901
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135894(5,6-Bis-(3-fluoro-4-methyl-phenyl)-7-thiophen-2-yl...)
Affinity DataIC50:  0.25nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135905(5-(4-Bromo-thiophen-2-yl)-6-(3,4-dimethoxy-phenyl)...)
Affinity DataIC50:  0.430nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135900(5,6-Diphenyl-7-thiophen-2-yl-pyrido[2,3-d]pyrimidi...)
Affinity DataIC50:  0.550nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135888(5-(4-Bromo-thiophen-2-yl)-6-(3,4-dimethoxy-phenyl)...)
Affinity DataIC50:  0.980nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135891(CHEMBL346622 | [4-Amino-5-(3-bromo-phenyl)-7-thiop...)
Affinity DataIC50:  3nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135899(5-(3-Bromo-phenyl)-6-(3,4-dimethoxy-phenyl)-7-(4-d...)
Affinity DataIC50:  3.10nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135898(7-(6-Dimethylamino-pyridin-3-yl)-5,6-diphenyl-pyri...)
Affinity DataIC50:  3.20nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135897(5-(3-Bromo-phenyl)-7-(6-morpholin-4-yl-pyridin-3-y...)
Affinity DataIC50:  4nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135889(5-(3-Bromo-phenyl)-6-(4-fluoro-phenyl)-7-(6-morpho...)
Affinity DataIC50:  5nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135893(5-(3-Chloro-phenyl)-7-(6-dimethylamino-pyridin-3-y...)
Affinity DataIC50:  5nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135904(7-(4-Dimethylamino-phenyl)-5,6-bis-(4-isopropyl-ph...)
Affinity DataIC50:  6.70nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095358(7-(4-Dimethylamino-phenyl)-5-phenyl-pyrido[2,3-d]p...)
Affinity DataIC50:  7nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135896(7-(4-Dimethylamino-phenyl)-5,6-diphenyl-pyrido[2,3...)
Affinity DataIC50:  16nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135905(5-(4-Bromo-thiophen-2-yl)-6-(3,4-dimethoxy-phenyl)...)
Affinity DataIC50:  25nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135906(5-(3-Chloro-phenyl)-6-(4-dimethylamino-phenyl)-7-(...)
Affinity DataIC50:  37nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135900(5,6-Diphenyl-7-thiophen-2-yl-pyrido[2,3-d]pyrimidi...)
Affinity DataIC50:  49nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135898(7-(6-Dimethylamino-pyridin-3-yl)-5,6-diphenyl-pyri...)
Affinity DataIC50:  53nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135895(5-(3-Bromo-phenyl)-7-(6-dimethylamino-pyridin-3-yl...)
Affinity DataIC50:  55nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135890(5-(4-Bromo-thiophen-2-yl)-6-cyclopropyl-7-(6-dimet...)
Affinity DataIC50:  60nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135902(6-Benzyl-5-(3-bromo-phenyl)-7-(6-morpholin-4-yl-py...)
Affinity DataIC50:  63nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135893(5-(3-Chloro-phenyl)-7-(6-dimethylamino-pyridin-3-y...)
Affinity DataIC50:  130nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135906(5-(3-Chloro-phenyl)-6-(4-dimethylamino-phenyl)-7-(...)
Affinity DataIC50:  130nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135897(5-(3-Bromo-phenyl)-7-(6-morpholin-4-yl-pyridin-3-y...)
Affinity DataIC50:  155nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135891(CHEMBL346622 | [4-Amino-5-(3-bromo-phenyl)-7-thiop...)
Affinity DataIC50:  163nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135889(5-(3-Bromo-phenyl)-6-(4-fluoro-phenyl)-7-(6-morpho...)
Affinity DataIC50:  197nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135896(7-(4-Dimethylamino-phenyl)-5,6-diphenyl-pyrido[2,3...)
Affinity DataIC50:  250nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135894(5,6-Bis-(3-fluoro-4-methyl-phenyl)-7-thiophen-2-yl...)
Affinity DataIC50:  288nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135901(5-(3-Bromo-phenyl)-6-cyclohexyl-7-(6-dimethylamino...)
Affinity DataIC50:  300nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135899(5-(3-Bromo-phenyl)-6-(3,4-dimethoxy-phenyl)-7-(4-d...)
Affinity DataIC50:  350nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135907(7-(4-Dimethylamino-phenyl)-6-phenyl-pyrido[2,3-d]p...)
Affinity DataIC50:  350nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135888(5-(4-Bromo-thiophen-2-yl)-6-(3,4-dimethoxy-phenyl)...)
Affinity DataIC50:  367nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135903(5-(3-Bromo-phenyl)-6-isopropyl-7-(6-morpholin-4-yl...)
Affinity DataIC50:  400nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135892(7-(4-Chloro-phenyl)-4-morpholin-4-yl-pteridine | C...)
Affinity DataIC50:  410nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095388(7-(4-Dimethylamino-phenyl)-pteridin-4-ylamine | CH...)
Affinity DataIC50:  440nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135902(6-Benzyl-5-(3-bromo-phenyl)-7-(6-morpholin-4-yl-py...)
Affinity DataIC50:  450nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095358(7-(4-Dimethylamino-phenyl)-5-phenyl-pyrido[2,3-d]p...)
Affinity DataIC50:  467nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135890(5-(4-Bromo-thiophen-2-yl)-6-cyclopropyl-7-(6-dimet...)
Affinity DataIC50:  625nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135895(5-(3-Bromo-phenyl)-7-(6-dimethylamino-pyridin-3-yl...)
Affinity DataIC50:  625nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095382(7-(4-Dimethylamino-phenyl)-pyrido[2,3-d]pyrimidin-...)
Affinity DataIC50:  773nMAssay Description:Inhibition adenosine kinase activity in rat brain in vitroMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135901(5-(3-Bromo-phenyl)-6-cyclohexyl-7-(6-dimethylamino...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135903(5-(3-Bromo-phenyl)-6-isopropyl-7-(6-morpholin-4-yl...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135904(7-(4-Dimethylamino-phenyl)-5,6-bis-(4-isopropyl-ph...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135907(7-(4-Dimethylamino-phenyl)-6-phenyl-pyrido[2,3-d]p...)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095388(7-(4-Dimethylamino-phenyl)-pteridin-4-ylamine | CH...)
Affinity DataIC50:  3.60E+3nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095382(7-(4-Dimethylamino-phenyl)-pyrido[2,3-d]pyrimidin-...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50135892(7-(4-Chloro-phenyl)-4-morpholin-4-yl-pteridine | C...)
Affinity DataIC50:  2.20E+4nMAssay Description:Inhibition of adenosine kinase activity in IMR-32 human neuroblastoma cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed