Compile Data Set for Download or QSAR
Report error Found 17 Enz. Inhib. hit(s) with all data for entry = 50007122 Sort by
TargetHistone deacetylase 8(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50397360(CHEMBL2170177 | US10188756, Compound CN110)
Affinity DataIC50: 12nMAssay Description:Inhibition of human recombinant HDAC8 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetHistone deacetylase 6(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50005711(GNF-Pf-1011 | CHEBI:46024 | TRICHOSTATIN | Trichos...)
Affinity DataIC50: 15nMAssay Description:Inhibition of human recombinant HDAC6 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetHistone deacetylase 8(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50506580(CHEMBL4517272)
Affinity DataIC50: 60nMAssay Description:Inhibition of human recombinant HDAC8 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetHistone deacetylase 8(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50506582(CHEMBL4448903)
Affinity DataIC50: 240nMAssay Description:Inhibition of human recombinant HDAC8 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetHistone deacetylase 8(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50005711(GNF-Pf-1011 | CHEBI:46024 | TRICHOSTATIN | Trichos...)
Affinity DataIC50: 280nMAssay Description:Inhibition of human recombinant HDAC8 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetHistone deacetylase 8(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50506578(CHEMBL4542119)
Affinity DataIC50: 340nMAssay Description:Inhibition of human recombinant HDAC8 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetHistone deacetylase 6(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50397360(CHEMBL2170177 | US10188756, Compound CN110)
Affinity DataIC50: 3.10E+3nMAssay Description:Inhibition of human recombinant HDAC6 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed
TargetHistone deacetylase 6(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50506579(CHEMBL4460757)
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibition of human recombinant HDAC6 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetHistone deacetylase 6(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50506580(CHEMBL4517272)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of human recombinant HDAC6 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetHistone deacetylase 11(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50506582(CHEMBL4448903)
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of human recombinant HDAC11 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetHistone deacetylase 8(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50506579(CHEMBL4460757)
Affinity DataIC50: 6.20E+3nMAssay Description:Inhibition of human recombinant HDAC8 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetHistone deacetylase 6(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50506582(CHEMBL4448903)
Affinity DataIC50: 6.90E+3nMAssay Description:Inhibition of human recombinant HDAC6 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetHistone deacetylase 11(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50506580(CHEMBL4517272)
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibition of human recombinant HDAC11 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetHistone deacetylase 11(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50506578(CHEMBL4542119)
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant HDAC11 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetHistone deacetylase 11(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50506581(CHEMBL4452476)
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of human recombinant HDAC11 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetHistone deacetylase 6(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50506578(CHEMBL4542119)
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of human recombinant HDAC6 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
PubMed
TargetHistone deacetylase 11(Human)
Paris-Saclay University

Curated by ChEMBL
LigandPNGBDBM50328678(6-(1,3-Dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-hexa...)
Affinity DataIC50: 2.20E+4nMAssay Description:Inhibition of human recombinant HDAC11 after 30 mins using fluorogenic substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
PubMed