Compile Data Set for Download or QSAR
Report error Found 42 Enz. Inhib. hit(s) with all data for entry = 50010958
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM14486(CHEMBL66280 | 5-Iodo-5-deoxytubercidin | 7-(5-deox...)
Affinity DataIC50: 1.60nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50094703(CHEMBL66089 | 5-(3-bromophenyl)-7-(6-morpholin-4-y...)
Affinity DataIC50: 1.70nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100580(5-(3-Bromo-phenyl)-7-(6-dimethylamino-pyridin-3-yl...)
Affinity DataIC50: 1.80nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50090895(2-[4-(4-Fluoro-phenylamino)-5-phenyl-pyrrolo[2,3-d...)
Affinity DataIC50: 2.80nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095384(5-(3-Bromo-phenyl)-7-(4-dimethylamino-phenyl)-pyri...)
Affinity DataIC50: 5nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095358(7-(4-Dimethylamino-phenyl)-5-phenyl-pyrido[2,3-d]p...)
Affinity DataIC50: 7nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095372(5-Cyclohexyl-7-(4-dimethylamino-phenyl)-pyrido[2,3...)
Affinity DataIC50: 8.30nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50090850((2R,3S,4R,5R)-2-Aminomethyl-5-(6-amino-purin-9-yl)...)
Affinity DataIC50: 15nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM14486(CHEMBL66280 | 5-Iodo-5-deoxytubercidin | 7-(5-deox...)
Affinity DataIC50: 22.8nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100584(7-(4-Dimethylamino-phenyl)-6-phenyl-pteridin-4-yla...)
Affinity DataIC50: 25nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100580(5-(3-Bromo-phenyl)-7-(6-dimethylamino-pyridin-3-yl...)
Affinity DataIC50: 32nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50094703(CHEMBL66089 | 5-(3-bromophenyl)-7-(6-morpholin-4-y...)
Affinity DataIC50: 50nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100588(6-(4-tert-Butyl-phenyl)-7-(4-dimethylamino-phenyl)...)
Affinity DataIC50: 62.5nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100586(3-[4-Amino-7-(4-dimethylamino-phenyl)-pyrido[2,3-d...)
Affinity DataIC50: 66.7nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100591(7-(4-Dimethylamino-phenyl)-6-p-tolyl-pyrido[2,3-d]...)
Affinity DataIC50: 73.3nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100583(7-(4-Dimethylamino-phenyl)-6-(4-methoxy-phenyl)-py...)
Affinity DataIC50: 91.7nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50090895(2-[4-(4-Fluoro-phenylamino)-5-phenyl-pyrrolo[2,3-d...)
Affinity DataIC50: 134nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095384(5-(3-Bromo-phenyl)-7-(4-dimethylamino-phenyl)-pyri...)
Affinity DataIC50: 167nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100584(7-(4-Dimethylamino-phenyl)-6-phenyl-pteridin-4-yla...)
Affinity DataIC50: 333nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100590(7-(4-Morpholin-4-yl-phenyl)-pteridin-4-ylamine | C...)
Affinity DataIC50: 400nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095388(7-(4-Dimethylamino-phenyl)-pteridin-4-ylamine | CH...)
Affinity DataIC50: 440nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095372(5-Cyclohexyl-7-(4-dimethylamino-phenyl)-pyrido[2,3...)
Affinity DataIC50: 467nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100591(7-(4-Dimethylamino-phenyl)-6-p-tolyl-pyrido[2,3-d]...)
Affinity DataIC50: 500nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100583(7-(4-Dimethylamino-phenyl)-6-(4-methoxy-phenyl)-py...)
Affinity DataIC50: 567nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100586(3-[4-Amino-7-(4-dimethylamino-phenyl)-pyrido[2,3-d...)
Affinity DataIC50: 700nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095382(7-(4-Dimethylamino-phenyl)-pyrido[2,3-d]pyrimidin-...)
Affinity DataIC50: 773nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100590(7-(4-Morpholin-4-yl-phenyl)-pteridin-4-ylamine | C...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100588(6-(4-tert-Butyl-phenyl)-7-(4-dimethylamino-phenyl)...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100589(7-(4-Amino-phenyl)-pteridin-4-ylamine | CHEMBL6704...)
Affinity DataIC50: 1.75E+3nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100581(7-(4-Methoxy-phenyl)-pteridin-4-ylamine | CHEMBL67...)
Affinity DataIC50: 2.00E+3nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100587(2-(6-Amino-5-nitro-pyrimidin-4-ylamino)-5-hydroxym...)
Affinity DataIC50: 2.00E+3nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50095388(7-(4-Dimethylamino-phenyl)-pteridin-4-ylamine | CH...)
Affinity DataIC50: 3.60E+3nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100585(7-(4-Nitro-phenyl)-pteridin-4-ylamine | CHEMBL3080...)
Affinity DataIC50: 4.75E+3nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Rat)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100582(7-Phenyl-pteridin-4-ylamine | CHEMBL419063)
Affinity DataIC50: 5.50E+3nMAssay Description:In vitro inhibition of Adenosine kinase (AK)More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50090850((2R,3S,4R,5R)-2-Aminomethyl-5-(6-amino-purin-9-yl)...)
Affinity DataIC50: 6.33E+3nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100589(7-(4-Amino-phenyl)-pteridin-4-ylamine | CHEMBL6704...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100585(7-(4-Nitro-phenyl)-pteridin-4-ylamine | CHEMBL3080...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100581(7-(4-Methoxy-phenyl)-pteridin-4-ylamine | CHEMBL67...)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100582(7-Phenyl-pteridin-4-ylamine | CHEMBL419063)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(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 phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetAdenosine kinase(Human)
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100587(2-(6-Amino-5-nitro-pyrimidin-4-ylamino)-5-hydroxym...)
Affinity DataIC50: 2.60E+4nMAssay Description:Inhibition of adenosine phosphorylation in confluent IMR-32 (human neuroblastoma) cells.More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed