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Found 62 with Last Name = 'kowaluk' and Initial = 'el'
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM14486((2R,3R,4S,5R)-2-(2-amino-9-iodo-3,5,7-triazabicycl...)
Affinity DataIC50:  1.60nMAssay Description:In vitro inhibition of Adenosine kinase of rat brain cytosol.More data for this Ligand-Target Pair
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50104168(4-Amino-6-((2R,3R,4S,5R)-5-aminomethyl-3,4-dihydro...)
Affinity DataIC50:  2nMAssay Description:In vitro inhibition of Adenosine kinase of rat brain cytosol.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167586(6-(3-Bromo-benzyl)-7-thiophen-2-yl-pyrido[2,3-d]py...)
Affinity DataIC50:  3.80nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50104164(4-((2R,3R,4S,5R)-5-Aminomethyl-3,4-dihydroxy-tetra...)
Affinity DataIC50:  4nMAssay Description:In vitro inhibition of Adenosine kinase of rat brain cytosol.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167584(6-(3-Bromo-4-methoxy-phenyl)-7-thiophen-2-yl-pyrid...)
Affinity DataIC50:  8nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167597(7-Thiophen-2-yl-6-p-tolyl-pyrido[2,3-d]pyrimidin-4...)
Affinity DataIC50:  9nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167599(6-Butyl-7-thiophen-2-yl-pyrido[2,3-d]pyrimidin-4-y...)
Affinity DataIC50:  11nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (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 of rat brain cytosol.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167585(6-(4-Bromo-phenyl)-7-(4-dimethylamino-phenyl)-pyri...)
Affinity DataIC50:  20nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167594(7-(4-Dimethylamino-phenyl)-6-pentyl-pyrido[2,3-d]p...)
Affinity DataIC50:  30nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167598(6-(3-Bromo-4-methoxy-phenyl)-7-(4-dimethylamino-ph...)
Affinity DataIC50:  33nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50104166((2R,3S,4R,5R)-2-Aminomethyl-5-(6-amino-5-nitro-pyr...)
Affinity DataIC50:  35nMAssay Description:In vitro inhibition of Adenosine kinase of rat brain cytosol.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167591(6-(3,4-Dimethoxy-phenyl)-7-thiophen-2-yl-pyrido[2,...)
Affinity DataIC50:  38nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167589(6-(3,4-Dimethoxy-phenyl)-7-(4-dimethylamino-phenyl...)
Affinity DataIC50:  45nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167590(7-Thiophen-3-yl-6-p-tolyl-pyrido[2,3-d]pyrimidin-4...)
Affinity DataIC50:  47nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167595(6-(3-Bromo-phenyl)-7-(4-dimethylamino-phenyl)-pyri...)
Affinity DataIC50:  70nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100583(7-(4-Dimethylamino-phenyl)-6-(4-methoxy-phenyl)-py...)
Affinity DataIC50:  92nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167588(6-Benzyl-7-(4-dimethylamino-phenyl)-pyrido[2,3-d]p...)
Affinity DataIC50:  114nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167601(7-{4-[((E)-2-Pyridin-2-yl)-vinyl]-phenyl}-6-p-toly...)
Affinity DataIC50:  115nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167587(7-(4-Pyrimidin-5-yl-phenyl)-6-p-tolyl-pyrido[2,3-d...)
Affinity DataIC50:  180nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167583(6,7-Bis-(4-dimethylamino-phenyl)-pyrido[2,3-d]pyri...)
Affinity DataIC50:  183nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167596(7-(4-Dimethylamino-phenyl)-6-isobutyl-pyrido[2,3-d...)
Affinity DataIC50:  200nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167598(6-(3-Bromo-4-methoxy-phenyl)-7-(4-dimethylamino-ph...)
Affinity DataIC50:  225nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167591(6-(3,4-Dimethoxy-phenyl)-7-thiophen-2-yl-pyrido[2,...)
Affinity DataIC50:  300nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More 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:  350nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167589(6-(3,4-Dimethoxy-phenyl)-7-(4-dimethylamino-phenyl...)
Affinity DataIC50:  350nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167583(6,7-Bis-(4-dimethylamino-phenyl)-pyrido[2,3-d]pyri...)
Affinity DataIC50:  367nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167584(6-(3-Bromo-4-methoxy-phenyl)-7-thiophen-2-yl-pyrid...)
Affinity DataIC50:  375nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167604(7-(4-Dimethylamino-phenyl)-6-phenethyl-pyrido[2,3-...)
Affinity DataIC50:  433nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More 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:  440nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167592(6-(4-Dimethylamino-phenyl)-7-pyridin-4-yl-pyrido[2...)
Affinity DataIC50:  467nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100583(7-(4-Dimethylamino-phenyl)-6-(4-methoxy-phenyl)-py...)
Affinity DataIC50:  567nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50104173(4-((2R,3R,4S,5R)-3,4-Dihydroxy-5-hydroxymethyl-tet...)
Affinity DataIC50:  600nMAssay Description:In vitro inhibition of Adenosine kinase of rat brain cytosol.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167586(6-(3-Bromo-benzyl)-7-thiophen-2-yl-pyrido[2,3-d]py...)
Affinity DataIC50:  650nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167588(6-Benzyl-7-(4-dimethylamino-phenyl)-pyrido[2,3-d]p...)
Affinity DataIC50:  650nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167594(7-(4-Dimethylamino-phenyl)-6-pentyl-pyrido[2,3-d]p...)
Affinity DataIC50:  700nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167599(6-Butyl-7-thiophen-2-yl-pyrido[2,3-d]pyrimidin-4-y...)
Affinity DataIC50:  767nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More 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:  773nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167597(7-Thiophen-2-yl-6-p-tolyl-pyrido[2,3-d]pyrimidin-4...)
Affinity DataIC50:  800nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167603(6-(3-Bromo-benzyl)-7-thiazol-2-yl-pyrido[2,3-d]pyr...)
Affinity DataIC50:  900nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167602(7-(4-Dimethylamino-phenyl)-6-(3-methoxy-phenyl)-py...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167600(7-Benzofuran-2-yl-6-p-tolyl-pyrido[2,3-d]pyrimidin...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167596(7-(4-Dimethylamino-phenyl)-6-isobutyl-pyrido[2,3-d...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167590(7-Thiophen-3-yl-6-p-tolyl-pyrido[2,3-d]pyrimidin-4...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167595(6-(3-Bromo-phenyl)-7-(4-dimethylamino-phenyl)-pyri...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167585(6-(4-Bromo-phenyl)-7-(4-dimethylamino-phenyl)-pyri...)
Affinity DataIC50: >1.00E+3nMAssay Description:Inhibitory concentration against Adenosine Kinase (intact cells)More 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:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Rattus norvegicus (rat))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50100587((2R,3R,4S,5R)-2-(6-Amino-5-nitro-pyrimidin-4-ylami...)
Affinity DataIC50:  2.00E+3nMAssay Description:In vitro inhibition of Adenosine kinase of rat brain cytosol.More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine kinase(Homo sapiens (Human))
Abbott Laboratories

Curated by ChEMBL
LigandPNGBDBM50167593(7-(4-Dimethylamino-phenyl)-6-(3-phenyl-propyl)-pyr...)
Affinity DataIC50:  2.23E+3nMAssay Description:Inhibitory concentration against Adenosine Kinase (enzyme)More 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:Inhibitory concentration against Adenosine Kinase (intact cells)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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