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Found 22 Enz. Inhib. hit(s) with all data for entry = 50016198
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50090887((1R,4S,5R)-2-Methyl-5-(5-phenyl-4-phenylamino-pyrr...)
Affinity DataIC50:  0.5nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50090881((2R,3R,4S,5R)-2-(6-Bromo-5-phenyl-4-phenylamino-py...)
Affinity DataIC50:  1nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166242((2R,3R,4S,5R)-2-[6-(2,3-Dihydro-indol-1-yl)-8-phen...)
Affinity DataIC50:  19nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166239((2R,3R,4S,5R)-2-[4-(2,3-Dihydro-indol-1-yl)-5-phen...)
Affinity DataIC50:  51nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166237((2R,3R,4S,5R)-2-[6-(2,3-Dihydro-indol-1-yl)-8-viny...)
Affinity DataIC50:  60nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166238((2R,3R,4S,5R)-2-(6,8-Bis-phenylamino-purin-9-yl)-5...)
Affinity DataIC50:  90nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166244((2R,3R,4S,5R)-2-[6-(2,3-Dihydro-indol-1-yl)-8-meth...)
Affinity DataIC50:  150nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50090850((2R,3S,4R,5R)-2-Aminomethyl-5-(6-amino-purin-9-yl)...)
Affinity DataIC50:  170nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166229((2R,3R,4S,5R)-2-[6-(2,3-Dihydro-indol-1-yl)-8-phen...)
Affinity DataIC50:  200nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166234((2R,3R,4S,5R)-2-[6-(2,3-Dihydro-indol-1-yl)-8-ethy...)
Affinity DataIC50:  230nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166232((2R,3S,4R,5R)-2-Hydroxymethyl-5-(6-phenylamino-8-v...)
Affinity DataIC50:  300nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166241((2R,3R,4S,5R)-2-[8-Chloro-6-(2,3-dihydro-indol-1-y...)
Affinity DataIC50:  480nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166245((2R,3R,4S,5R)-2-[6-(2,3-Dihydro-indol-1-yl)-purin-...)
Affinity DataIC50:  500nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166240((2R,3S,4R,5R)-2-Hydroxymethyl-5-(8-methylsulfanyl-...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166228((2R,3R,4S,5R)-2-[6-(2,3-Dihydro-indol-1-yl)-8-iodo...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166246((2R,3R,4S,5R)-2-[6-(2,3-Dihydro-indol-1-yl)-8-ethy...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166231((2R,3R,4S,5R)-2-[6,8-Bis-(2,3-dihydro-indol-1-yl)-...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166230((2R,3R,4S,5R)-2-[6-(2,3-Dihydro-indol-1-yl)-8-fura...)
Affinity DataIC50:  2.90E+3nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166236((2R,3R,4S,5R)-2-(8-Chloro-6-phenylamino-purin-9-yl...)
Affinity DataIC50:  3.60E+3nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166243((2R,3S,4R,5R)-2-Hydroxymethyl-5-(8-iodo-6-phenylam...)
Affinity DataIC50:  4.50E+3nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166235((2R,3R,4S,5R)-2-(8-Furan-2-yl-6-phenylamino-purin-...)
Affinity DataIC50:  6.90E+3nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50166233((2R,3R,4S,5R)-2-[8-(2,3-Dihydro-indol-1-yl)-6-phen...)
Affinity DataIC50:  7.10E+3nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed