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Found 170 with Last Name = 'le guével' and Initial = 'r'
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50304109((Z)-5'-Nitro-1H,1'H-[2,3']biindolylidene-3,2'-dion...)
Affinity DataIC50:  6nMAssay Description:Inhibition of GST-fused CDK5/p25 expressed in Escherichia coli assessed as [gamma-33P]ATP incorporation after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314133(CHEMBL1093713 | N-(3,5-Dimethylphenyl)-N'-hydroxyo...)
Affinity DataIC50:  17nMAssay Description:Ex vivo inhibition of human HDAC1 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50304111(CHEMBL593698 | N-((Z)-3,2'-Dioxo-1,3,1',2'-tetrahy...)
Affinity DataIC50:  18nMAssay Description:Inhibition of GST-fused CDK5/p25 expressed in Escherichia coli assessed as [gamma-33P]ATP incorporation after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399310(CHEMBL2180854)
Affinity DataIC50:  25nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314134(CHEMBL1093041 | N-(3-Ethylphenyl)-N'-hydroxyoctane...)
Affinity DataIC50:  27nMAssay Description:Ex vivo inhibition of human HDAC1 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314133(CHEMBL1093713 | N-(3,5-Dimethylphenyl)-N'-hydroxyo...)
Affinity DataIC50:  30nMAssay Description:Ex vivo inhibition of human HDAC3 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314135(CHEMBL1093359 | N-(3,4-Dimethylphenyl)-N'-hydroxyo...)
Affinity DataIC50:  30nMAssay Description:Ex vivo inhibition of human HDAC1 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314134(CHEMBL1093041 | N-(3-Ethylphenyl)-N'-hydroxyoctane...)
Affinity DataIC50:  35nMAssay Description:Ex vivo inhibition of human HDAC3 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399303(CHEMBL2180844)
Affinity DataIC50:  37nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399312(CHEMBL2180852)
Affinity DataIC50:  40nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50304121((Z)-5-Bromo-5'-nitro-1H,1'H-[2,3']biindolylidene-3...)
Affinity DataIC50:  50nMAssay Description:Inhibition of GST-fused CDK5/p25 expressed in Escherichia coli assessed as [gamma-33P]ATP incorporation after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314135(CHEMBL1093359 | N-(3,4-Dimethylphenyl)-N'-hydroxyo...)
Affinity DataIC50:  56nMAssay Description:Ex vivo inhibition of human HDAC3 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314136(CHEMBL1089339 | N-Hydroxy-N'-(3-methylphenyl)octan...)
Affinity DataIC50:  57nMAssay Description:Ex vivo inhibition of human HDAC1 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314136(CHEMBL1089339 | N-Hydroxy-N'-(3-methylphenyl)octan...)
Affinity DataIC50:  58nMAssay Description:Ex vivo inhibition of human HDAC3 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50355909(CHEMBL1910195)
Affinity DataIC50:  60nMAssay Description:Inhibition of rat recombinant GST-fused DYRK1A expressed in Escherichia coli using myelin protein and [33P-gamma]-ATP after 30 mins by scintillation ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399315(CHEMBL2180849)
Affinity DataIC50:  68nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399326(CHEMBL2180863)
Affinity DataIC50:  70nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314137(CHEMBL1091487 | N-Hydroxy-N'-(4-methoxyphenyl)octa...)
Affinity DataIC50:  71nMAssay Description:Ex vivo inhibition of human HDAC1 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399301(CHEMBL2180862)
Affinity DataIC50:  75nMAssay Description:Inhibition of CDK1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314138(CHEMBL1092762 | N-Hydroxy-N'-(4-methylphenyl)octan...)
Affinity DataIC50:  76nMAssay Description:Ex vivo inhibition of human HDAC1 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399301(CHEMBL2180862)
Affinity DataIC50:  80nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399309(CHEMBL2180855)
Affinity DataIC50:  90nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50304113(CHEMBL604270 | N-((Z)-5-Bromo-3,2'-dioxo-1,3,1',2'...)
Affinity DataIC50:  110nMAssay Description:Inhibition of GST-fused CDK5/p25 expressed in Escherichia coli assessed as [gamma-33P]ATP incorporation after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314138(CHEMBL1092762 | N-Hydroxy-N'-(4-methylphenyl)octan...)
Affinity DataIC50:  114nMAssay Description:Ex vivo inhibition of human HDAC3 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  119nMAssay Description:Ex vivo inhibition of human HDAC1 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50423711(CHEMBL594403)
Affinity DataIC50:  120nMAssay Description:Inhibition of GST-fused CDK5/p25 expressed in Escherichia coli assessed as [gamma-33P]ATP incorporation after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399311(CHEMBL2180853)
Affinity DataIC50:  130nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314137(CHEMBL1091487 | N-Hydroxy-N'-(4-methoxyphenyl)octa...)
Affinity DataIC50:  137nMAssay Description:Ex vivo inhibition of human HDAC3 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  147nMAssay Description:Ex vivo inhibition of human HDAC3 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMedDrugBank

TargetHistone deacetylase 1(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314139(CHEMBL1093042 | N-(4-Ethylphenyl)-N'-hydroxyoctane...)
Affinity DataIC50:  149nMAssay Description:Ex vivo inhibition of human HDAC1 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50304112((Z)-5'-Amino-1H,1'H-[2,3']biindolylidene-3,2'-dion...)
Affinity DataIC50:  150nMAssay Description:Inhibition of GST-fused CDK5/p25 expressed in Escherichia coli assessed as [gamma-33P]ATP incorporation after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50304114(CHEMBL445348 | N-{(Z)-3-[(E)-Hydroxyimino]-2'-oxo-...)
Affinity DataIC50:  160nMAssay Description:Inhibition of GST-fused CDK5/p25 expressed in Escherichia coli assessed as [gamma-33P]ATP incorporation after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50355909(CHEMBL1910195)
Affinity DataIC50:  160nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 and [33P-gamma]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399320(CHEMBL2180869)
Affinity DataIC50:  170nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50423712(CHEMBL593968)
Affinity DataIC50:  200nMAssay Description:Inhibition of GST-fused CDK5/p25 expressed in Escherichia coli assessed as [gamma-33P]ATP incorporation after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50355915(CHEMBL1910201)
Affinity DataIC50:  230nMAssay Description:Inhibition of rat recombinant GST-fused DYRK1A expressed in Escherichia coli using myelin protein and [33P-gamma]-ATP after 30 mins by scintillation ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314139(CHEMBL1093042 | N-(4-Ethylphenyl)-N'-hydroxyoctane...)
Affinity DataIC50:  240nMAssay Description:Ex vivo inhibition of human HDAC3 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399308(CHEMBL2180856)
Affinity DataIC50:  260nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50355916(CHEMBL1910377)
Affinity DataIC50:  300nMAssay Description:Inhibition of rat recombinant GST-fused DYRK1A expressed in Escherichia coli using myelin protein and [33P-gamma]-ATP after 30 mins by scintillation ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50423713(CHEMBL606982)
Affinity DataIC50:  300nMAssay Description:Inhibition of GST-fused CDK5/p25 expressed in Escherichia coli assessed as [gamma-33P]ATP incorporation after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50355906(CHEMBL1910192)
Affinity DataIC50:  340nMAssay Description:Inhibition of rat recombinant GST-fused DYRK1A expressed in Escherichia coli using myelin protein and [33P-gamma]-ATP after 30 mins by scintillation ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50355911(CHEMBL1910197)
Affinity DataIC50:  350nMAssay Description:Inhibition of rat recombinant GST-fused DYRK1A expressed in Escherichia coli using myelin protein and [33P-gamma]-ATP after 30 mins by scintillation ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50355915(CHEMBL1910201)
Affinity DataIC50:  360nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 and [33P-gamma]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50355911(CHEMBL1910197)
Affinity DataIC50:  380nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 and [33P-gamma]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399323(CHEMBL2180866)
Affinity DataIC50:  430nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399319(CHEMBL2180870)
Affinity DataIC50:  510nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50399322(CHEMBL2180867)
Affinity DataIC50:  530nMAssay Description:Inhibition of human recombinant CDK5/p25 using histone H1 as substrate and [gamma-33P]-ATP after 30 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
LigandPNGBDBM50355912(CHEMBL1910198)
Affinity DataIC50:  540nMAssay Description:Inhibition of rat recombinant GST-fused DYRK1A expressed in Escherichia coli using myelin protein and [33P-gamma]-ATP after 30 mins by scintillation ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCyclin-dependent kinase 5 activator 1(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50304119((Z)-5'-Amino-5-bromo-1H,1'H-[2,3']biindolylidene-3...)
Affinity DataIC50:  550nMAssay Description:Inhibition of GST-fused CDK5/p25 expressed in Escherichia coli assessed as [gamma-33P]ATP incorporation after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Umr Cnrs 6026-Universit£

Curated by ChEMBL
LigandPNGBDBM50314140(CHEMBL1076794 | N-Hydroxy-N'-(2-methylphenyl)octan...)
Affinity DataIC50:  576nMAssay Description:Ex vivo inhibition of human HDAC1 in human Caco2 cells by flurometric cellular activity assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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