Compile Data Set for Download or QSAR
Report error Found 22 Enz. Inhib. hit(s) with all data for entry = 50016198
TargetAdenosine kinase(Human)
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50090887(5-phenyl-4-(phenylamino)-7-(5-deoxy-beta-D-ribofur...)
Affinity DataIC50: 0.5nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Metabasis Therapeutics

Curated by ChEMBL
LigandPNGBDBM50090881(2-(6-Bromo-5-phenyl-4-phenylamino-pyrrolo[2,3-d]py...)
Affinity DataIC50: 1nMAssay Description:Inhibitory activity against Human Recombinant Adenosine KinaseMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed