Compile Data Set for Download or QSAR
maximum 50k data
Found 38 Enz. Inhib. hit(s) with all data for entry = 50026902
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50240935(CHEMBL181459 | N1-(2-(hydroxycarbamoyl)phenyl)-N8-...)
Affinity DataIC50:  550nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50240935(CHEMBL181459 | N1-(2-(hydroxycarbamoyl)phenyl)-N8-...)
Affinity DataIC50:  590nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244813((E)-N-Hydroxy-3-(5-((E)-3-oxo-3-p-tolylprop-1-enyl...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244818((E)-N-Hydroxy-3-(5-((E)-3-(naphthalen-2-yl)-3-oxop...)
Affinity DataIC50:  3.77E+3nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244817((E)-N-Hydroxy-3-(5-((E)-3-(6-methoxynaphthalen-2-y...)
Affinity DataIC50:  4.04E+3nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244869((E)-3-(5-((E)-3-(2,4-Dichlorophenyl)-3-oxoprop-1-e...)
Affinity DataIC50:  4.29E+3nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244868((E)-3-(5-((E)-3-(2,5-Dichlorophenyl)-3-oxoprop-1-e...)
Affinity DataIC50:  4.31E+3nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244818((E)-N-Hydroxy-3-(5-((E)-3-(naphthalen-2-yl)-3-oxop...)
Affinity DataIC50:  4.38E+3nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244868((E)-3-(5-((E)-3-(2,5-Dichlorophenyl)-3-oxoprop-1-e...)
Affinity DataIC50:  4.72E+3nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244814((E)-N-Hydroxy-3-(5-((E)-3-(4-isopropylphenyl)-3-ox...)
Affinity DataIC50:  4.89E+3nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244816((E)-3-(5-((E)-3-(4-Chlorophenyl)-3-oxoprop-1-enyl)...)
Affinity DataIC50:  6.03E+3nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244870((E)-3-(5-((E)-3-(4-Fluorophenyl)-3-oxoprop-1-enyl)...)
Affinity DataIC50:  7.68E+3nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244869((E)-3-(5-((E)-3-(2,4-Dichlorophenyl)-3-oxoprop-1-e...)
Affinity DataIC50:  8.19E+3nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244922((E)-5-(4-(Benzyloxy)-3-methoxystyryl)-N-hydroxyfur...)
Affinity DataIC50:  1.03E+4nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244817((E)-N-Hydroxy-3-(5-((E)-3-(6-methoxynaphthalen-2-y...)
Affinity DataIC50:  1.10E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244871((E)-N-Hydroxy-3-(5-((E)-3-oxo-3-phenylprop-1-enyl)...)
Affinity DataIC50:  1.16E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244815((E)-3-(5-((E)-3-(3-Chlorophenyl)-3-oxoprop-1-enyl)...)
Affinity DataIC50:  1.26E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244815((E)-3-(5-((E)-3-(3-Chlorophenyl)-3-oxoprop-1-enyl)...)
Affinity DataIC50:  1.29E+4nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244813((E)-N-Hydroxy-3-(5-((E)-3-oxo-3-p-tolylprop-1-enyl...)
Affinity DataIC50:  1.32E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244922((E)-5-(4-(Benzyloxy)-3-methoxystyryl)-N-hydroxyfur...)
Affinity DataIC50:  1.34E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244870((E)-3-(5-((E)-3-(4-Fluorophenyl)-3-oxoprop-1-enyl)...)
Affinity DataIC50:  1.50E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244816((E)-3-(5-((E)-3-(4-Chlorophenyl)-3-oxoprop-1-enyl)...)
Affinity DataIC50:  1.57E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244871((E)-N-Hydroxy-3-(5-((E)-3-oxo-3-phenylprop-1-enyl)...)
Affinity DataIC50:  2.28E+4nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244814((E)-N-Hydroxy-3-(5-((E)-3-(4-isopropylphenyl)-3-ox...)
Affinity DataIC50:  2.41E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244919((E)-5-(2,3-Dichlorostyryl)-N-hydroxyfuran-2-carbox...)
Affinity DataIC50:  2.53E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244918((E)-5-(2-(Benzo[d][1,3]dioxol-5-yl)vinyl)-N-hydrox...)
Affinity DataIC50:  2.96E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244920((E)-N-Hydroxy-5-(2-hydroxy-3-methoxystyryl)furan-2...)
Affinity DataIC50:  4.28E+4nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244873((E)-N-Hydroxy-5-(4-hydroxystyryl)furan-2-carboxami...)
Affinity DataIC50:  4.31E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244874((E)-N-Hydroxy-5-(2-hydroxystyryl)furan-2-carboxami...)
Affinity DataIC50:  4.71E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244872((E)-N-Hydroxy-5-styrylfuran-2-carboxamide | CHEMBL...)
Affinity DataIC50:  4.72E+4nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244872((E)-N-Hydroxy-5-styrylfuran-2-carboxamide | CHEMBL...)
Affinity DataIC50:  4.92E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244919((E)-5-(2,3-Dichlorostyryl)-N-hydroxyfuran-2-carbox...)
Affinity DataIC50:  4.93E+4nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244921((E)-5-(4-(Dimethylamino)styryl)-N-hydroxyfuran-2-c...)
Affinity DataIC50:  4.94E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244920((E)-N-Hydroxy-5-(2-hydroxy-3-methoxystyryl)furan-2...)
Affinity DataIC50:  5.01E+4nMAssay Description:Inhibition of human recombinant HDAC1 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244921((E)-5-(4-(Dimethylamino)styryl)-N-hydroxyfuran-2-c...)
Affinity DataIC50:  5.06E+4nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244873((E)-N-Hydroxy-5-(4-hydroxystyryl)furan-2-carboxami...)
Affinity DataIC50:  5.71E+4nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244874((E)-N-Hydroxy-5-(2-hydroxystyryl)furan-2-carboxami...)
Affinity DataIC50:  7.42E+4nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
China Pharmaceutical University

Curated by ChEMBL
LigandPNGBDBM50244918((E)-5-(2-(Benzo[d][1,3]dioxol-5-yl)vinyl)-N-hydrox...)
Affinity DataIC50:  8.56E+4nMAssay Description:Inhibition of human recombinant HDAC4 using Fluor de Lys as substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed