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Found 38 with Last Name = 'bowler' and Initial = 'an'
TargetAdenosine receptor A3(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM21221((2S,3S,4R,5R)-5-(2-chloro-6-{[(3-iodophenyl)methyl...)
Affinity DataKi:  1.10nMAssay Description:Binding affinity for adenosine A3 receptor as inhibition of [125I]-AB-MECA binding to human receptor expressed in HEK 293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50070866((2R,3R,4S,5R)-2-[2-Chloro-6-(3-iodo-benzylamino)-p...)
Affinity DataKi:  7.80nMAssay Description:Binding affinity for adenosine A3 receptor as inhibition of [125I]-AB-MECA binding to human receptor expressed in HEK 293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50070867((2R,3R,4S,5R)-2-(2-Chloro-6-methoxyamino-purin-9-y...)
Affinity DataKi:  20nMAssay Description:Binding affinity for adenosine A3 receptor as inhibition of [125I]-AB-MECA binding to human receptor expressed in HEK 293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50070864((2R,3R,4S,5S)-2-(2-Chloro-6-methoxyamino-purin-9-y...)
Affinity DataKi:  26nMAssay Description:Binding affinity for adenosine A3 receptor as inhibition of [125I]-AB-MECA binding to human receptor expressed in HEK 293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50070865((2R,3R,4S,5R)-2-(2-Chloro-6-methoxyamino-purin-9-y...)
Affinity DataKi:  31nMAssay Description:Binding affinity for adenosine A3 receptor as inhibition of [125I]-AB-MECA binding to human receptor expressed in HEK 293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50070863((2S,3S,4R,5R)-5-(6-Benzylamino-purin-9-yl)-3,4-dih...)
Affinity DataKi:  41nMAssay Description:Binding affinity for adenosine A3 receptor as inhibition of [125I]-AB-MECA binding to human receptor expressed in HEK 293 cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
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Curated by ChEMBL
LigandPNGBDBM21221((2S,3S,4R,5R)-5-(2-chloro-6-{[(3-iodophenyl)methyl...)
Affinity DataKi:  54nMAssay Description:Binding affinity for adenosine A1 receptor as inhibition of 3[H]-R-PIA binding in rat brainMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
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Curated by ChEMBL
LigandPNGBDBM21221((2S,3S,4R,5R)-5-(2-chloro-6-{[(3-iodophenyl)methyl...)
Affinity DataKi:  56nMAssay Description:Binding affinity for adenosine A2a receptor as inhibition of 3[H]-CGS 21680 binding in rat striatumMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50070864((2R,3R,4S,5S)-2-(2-Chloro-6-methoxyamino-purin-9-y...)
Affinity DataKi:  74nMAssay Description:Binding affinity for adenosine A1 receptor as inhibition of 3[H]-R-PIA binding in rat brainMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50070865((2R,3R,4S,5R)-2-(2-Chloro-6-methoxyamino-purin-9-y...)
Affinity DataKi:  620nMAssay Description:Binding affinity for adenosine A1 receptor as inhibition of 3[H]-R-PIA binding in rat brainMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50070867((2R,3R,4S,5R)-2-(2-Chloro-6-methoxyamino-purin-9-y...)
Affinity DataKi:  1.23E+3nMAssay Description:Binding affinity for adenosine A1 receptor as inhibition of 3[H]-R-PIA binding in rat brainMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50070866((2R,3R,4S,5R)-2-[2-Chloro-6-(3-iodo-benzylamino)-p...)
Affinity DataKi:  1.90E+3nMAssay Description:Binding affinity for adenosine A2a receptor as inhibition of 3[H]-CGS 21680 binding in rat striatumMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50070866((2R,3R,4S,5R)-2-[2-Chloro-6-(3-iodo-benzylamino)-p...)
Affinity DataKi:  1.90E+3nMAssay Description:Binding affinity for adenosine A1 receptor as inhibition of 3[H]-R-PIA binding in rat brainMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50070863((2S,3S,4R,5R)-5-(6-Benzylamino-purin-9-yl)-3,4-dih...)
Affinity DataKi:  2.10E+3nMAssay Description:Binding affinity for adenosine A2a receptor as inhibition of 3[H]-CGS 21680 binding in rat striatumMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50070863((2S,3S,4R,5R)-5-(6-Benzylamino-purin-9-yl)-3,4-dih...)
Affinity DataKi:  2.40E+3nMAssay Description:Binding affinity for adenosine A1 receptor as inhibition of 3[H]-R-PIA binding in rat brainMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50070864((2R,3R,4S,5S)-2-(2-Chloro-6-methoxyamino-purin-9-y...)
Affinity DataKi:  4.65E+3nMAssay Description:Binding affinity for adenosine A2a receptor as inhibition of 3[H]-CGS 21680 binding in rat striatumMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50070865((2R,3R,4S,5R)-2-(2-Chloro-6-methoxyamino-purin-9-y...)
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity for adenosine A2a receptor as inhibition of 3[H]-CGS 21680 binding in rat striatumMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50070867((2R,3R,4S,5R)-2-(2-Chloro-6-methoxyamino-purin-9-y...)
Affinity DataKi: >1.00E+4nMAssay Description:Binding affinity for adenosine A2a receptor as inhibition of 3[H]-CGS 21680 binding in rat striatumMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50130727(1-(4-Amino-furazan-3-yl)-5-pyrrolidin-1-ylmethyl-1...)
Affinity DataIC50:  100nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130724(1-(4-Amino-furazan-3-yl)-5-piperidin-1-ylmethyl-1H...)
Affinity DataIC50:  100nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50059889((staurosporine)3-methoxy-2-methyl-4-methylamino-(2...)
Affinity DataIC50:  160nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50130732(4-[4-(5-Pyridin-4-yl-4H-[1,2,4]triazol-3-yl)-5-pyr...)
Affinity DataIC50:  240nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130719(4-[5-Piperidin-1-ylmethyl-4-(5-pyridin-4-yl-4H-[1,...)
Affinity DataIC50:  280nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50130725(3-(3-Chloro-4-hydroxy-phenylamino)-4-(2-nitro-phen...)
Affinity DataIC50:  380nMAssay Description:Inhibition of Cyclin-dependent kinase 2-cyclin AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130725(3-(3-Chloro-4-hydroxy-phenylamino)-4-(2-nitro-phen...)
Affinity DataIC50:  380nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130730(1-(4-Amino-furazan-3-yl)-5-diethylaminomethyl-1H-[...)
Affinity DataIC50:  410nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130720(1-(4-Amino-furazan-3-yl)-5-piperidin-1-ylmethyl-1H...)
Affinity DataIC50:  1.16E+3nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130726(1-(4-Amino-furazan-3-yl)-5-pyrrolidin-1-ylmethyl-1...)
Affinity DataIC50:  2.10E+3nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130722(4-[5-Dimethylaminomethyl-4-(5-pyridin-4-yl-4H-[1,2...)
Affinity DataIC50:  6.92E+3nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130733(1-(4-Amino-furazan-3-yl)-5-piperidin-1-ylmethyl-1H...)
Affinity DataIC50:  9.30E+3nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130731(1-(4-Amino-furazan-3-yl)-5-piperidin-1-ylmethyl-1H...)
Affinity DataIC50:  9.60E+3nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130728(1-(4-Amino-furazan-3-yl)-5-diethylaminomethyl-1H-[...)
Affinity DataIC50:  1.17E+4nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130721(1-(4-Amino-furazan-3-yl)-5-diethylaminomethyl-1H-[...)
Affinity DataIC50:  1.70E+4nMAssay Description:Inhibition of human Glycogen synthase kinase-3 beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50130724(1-(4-Amino-furazan-3-yl)-5-piperidin-1-ylmethyl-1H...)
Affinity DataIC50:  9.60E+4nMAssay Description:Inhibition of Cyclin-dependent kinase 2-cyclin AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50130720(1-(4-Amino-furazan-3-yl)-5-piperidin-1-ylmethyl-1H...)
Affinity DataIC50:  1.19E+5nMAssay Description:Inhibition of Cyclin-dependent kinase 2-cyclin AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130729(1-(4-Amino-furazan-3-yl)-5-(isobutylamino-methyl)-...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2(Homo sapiens (Human))
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Curated by ChEMBL
LigandPNGBDBM50130719(4-[5-Piperidin-1-ylmethyl-4-(5-pyridin-4-yl-4H-[1,...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of Cyclin-dependent kinase 2-cyclin AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGlycogen synthase kinase-3 beta(Homo sapiens (Human))
Novo Nordisk

Curated by ChEMBL
LigandPNGBDBM50130723(1-(4-Amino-furazan-3-yl)-5-piperidin-1-ylmethyl-1H...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibitory activity against human glycogen synthase kinase-3beta (GSK3-beta) at 100 uM ATPMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed