Compile Data Set for Download or QSAR
Found 51 Enz. Inhib. hit(s) with all data for entry = 50030522
TargetHistone deacetylase 6(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297445(CHEMBL561483 | N-hydroxy-7,7-bis(7-methoxy-1H-indo...)copy SMILEScopy InChI
Affinity DataIC50: 2.60nMAssay Description:Inhibition of human HDAC6 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297444(CHEMBL564876 | N-hydroxy-7,7-di(1H-indol-3-yl)hept...)copy SMILEScopy InChI
Affinity DataIC50: 6nMAssay Description:Inhibition of human HDAC6 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297446(CHEMBL561604 | N-hydroxy-7,7-bis(5-nitro-1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 18nMAssay Description:Inhibition of human HDAC3 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297446(CHEMBL561604 | N-hydroxy-7,7-bis(5-nitro-1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 20nMAssay Description:Inhibition of human HDAC6 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297445(CHEMBL561483 | N-hydroxy-7,7-bis(7-methoxy-1H-indo...)copy SMILEScopy InChI
Affinity DataIC50: 23nMAssay Description:Inhibition of human HDAC3 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297445(CHEMBL561483 | N-hydroxy-7,7-bis(7-methoxy-1H-indo...)copy SMILEScopy InChI
Affinity DataIC50: 83nMAssay Description:Inhibition of human HDAC1 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297446(CHEMBL561604 | N-hydroxy-7,7-bis(5-nitro-1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of human HDAC5 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297446(CHEMBL561604 | N-hydroxy-7,7-bis(5-nitro-1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of human HDAC1 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297446(CHEMBL561604 | N-hydroxy-7,7-bis(5-nitro-1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 150nMAssay Description:Inhibition of human HDAC9 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297445(CHEMBL561483 | N-hydroxy-7,7-bis(7-methoxy-1H-indo...)copy SMILEScopy InChI
Affinity DataIC50: 180nMAssay Description:Inhibition of human HDAC8 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297446(CHEMBL561604 | N-hydroxy-7,7-bis(5-nitro-1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of human HDAC4 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297446(CHEMBL561604 | N-hydroxy-7,7-bis(5-nitro-1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of human HDAC7 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297445(CHEMBL561483 | N-hydroxy-7,7-bis(7-methoxy-1H-indo...)copy SMILEScopy InChI
Affinity DataIC50: 220nMAssay Description:Inhibition of human HDAC4 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297445(CHEMBL561483 | N-hydroxy-7,7-bis(7-methoxy-1H-indo...)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Inhibition of human HDAC10 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297444(CHEMBL564876 | N-hydroxy-7,7-di(1H-indol-3-yl)hept...)copy SMILEScopy InChI
Affinity DataIC50: 240nMAssay Description:Inhibition of human HDAC8 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297446(CHEMBL561604 | N-hydroxy-7,7-bis(5-nitro-1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 250nMAssay Description:Inhibition of human HDAC10 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297448(CHEMBL564916 | N-(2-aminophenyl)-7,7-di(1H-indol-3...)copy SMILEScopy InChI
Affinity DataIC50: 260nMAssay Description:Inhibition of human HDAC3 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297445(CHEMBL561483 | N-hydroxy-7,7-bis(7-methoxy-1H-indo...)copy SMILEScopy InChI
Affinity DataIC50: 311nMAssay Description:Inhibition of human HDAC5 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297445(CHEMBL561483 | N-hydroxy-7,7-bis(7-methoxy-1H-indo...)copy SMILEScopy InChI
Affinity DataIC50: 340nMAssay Description:Inhibition of human HDAC9 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297444(CHEMBL564876 | N-hydroxy-7,7-di(1H-indol-3-yl)hept...)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of human HDAC3 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 11(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297447(3-(4-(di(1H-indol-3-yl)methyl)phenyl)-N-hydroxyacr...)copy SMILEScopy InChI
Affinity DataIC50: 410nMAssay Description:Inhibition of human HDAC11 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297445(CHEMBL561483 | N-hydroxy-7,7-bis(7-methoxy-1H-indo...)copy SMILEScopy InChI
Affinity DataIC50: 420nMAssay Description:Inhibition of human HDAC7 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 11(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297444(CHEMBL564876 | N-hydroxy-7,7-di(1H-indol-3-yl)hept...)copy SMILEScopy InChI
Affinity DataIC50: 430nMAssay Description:Inhibition of human HDAC11 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297447(3-(4-(di(1H-indol-3-yl)methyl)phenyl)-N-hydroxyacr...)copy SMILEScopy InChI
Affinity DataIC50: 440nMAssay Description:Inhibition of human HDAC3 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297445(CHEMBL561483 | N-hydroxy-7,7-bis(7-methoxy-1H-indo...)copy SMILEScopy InChI
Affinity DataIC50: 440nMAssay Description:Inhibition of human HDAC2 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297444(CHEMBL564876 | N-hydroxy-7,7-di(1H-indol-3-yl)hept...)copy SMILEScopy InChI
Affinity DataIC50: 530nMAssay Description:Inhibition of human HDAC7 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297444(CHEMBL564876 | N-hydroxy-7,7-di(1H-indol-3-yl)hept...)copy SMILEScopy InChI
Affinity DataIC50: 590nMAssay Description:Inhibition of human HDAC5 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297446(CHEMBL561604 | N-hydroxy-7,7-bis(5-nitro-1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 590nMAssay Description:Inhibition of human HDAC2 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297446(CHEMBL561604 | N-hydroxy-7,7-bis(5-nitro-1H-indol-...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:Inhibition of human HDAC8 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297444(CHEMBL564876 | N-hydroxy-7,7-di(1H-indol-3-yl)hept...)copy SMILEScopy InChI
Affinity DataIC50: 640nMAssay Description:Inhibition of human HDAC9 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297444(CHEMBL564876 | N-hydroxy-7,7-di(1H-indol-3-yl)hept...)copy SMILEScopy InChI
Affinity DataIC50: 730nMAssay Description:Inhibition of human HDAC1 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297447(3-(4-(di(1H-indol-3-yl)methyl)phenyl)-N-hydroxyacr...)copy SMILEScopy InChI
Affinity DataIC50: 730nMAssay Description:Inhibition of human HDAC8 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297444(CHEMBL564876 | N-hydroxy-7,7-di(1H-indol-3-yl)hept...)copy SMILEScopy InChI
Affinity DataIC50: 870nMAssay Description:Inhibition of human HDAC10 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297448(CHEMBL564916 | N-(2-aminophenyl)-7,7-di(1H-indol-3...)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of human HDAC2 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297444(CHEMBL564876 | N-hydroxy-7,7-di(1H-indol-3-yl)hept...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+3nMAssay Description:Inhibition of human HDAC4 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297444(CHEMBL564876 | N-hydroxy-7,7-di(1H-indol-3-yl)hept...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of human HDAC2 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297447(3-(4-(di(1H-indol-3-yl)methyl)phenyl)-N-hydroxyacr...)copy SMILEScopy InChI
Affinity DataIC50: 3.30E+3nMAssay Description:Inhibition of human HDAC9 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297447(3-(4-(di(1H-indol-3-yl)methyl)phenyl)-N-hydroxyacr...)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+3nMAssay Description:Inhibition of human HDAC2 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297447(3-(4-(di(1H-indol-3-yl)methyl)phenyl)-N-hydroxyacr...)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibition of human HDAC7 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297447(3-(4-(di(1H-indol-3-yl)methyl)phenyl)-N-hydroxyacr...)copy SMILEScopy InChI
Affinity DataIC50: 4.70E+3nMAssay Description:Inhibition of human HDAC10 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297447(3-(4-(di(1H-indol-3-yl)methyl)phenyl)-N-hydroxyacr...)copy SMILEScopy InChI
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of human HDAC1 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297447(3-(4-(di(1H-indol-3-yl)methyl)phenyl)-N-hydroxyacr...)copy SMILEScopy InChI
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of human HDAC4 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297447(3-(4-(di(1H-indol-3-yl)methyl)phenyl)-N-hydroxyacr...)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of human HDAC6 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297447(3-(4-(di(1H-indol-3-yl)methyl)phenyl)-N-hydroxyacr...)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of human HDAC5 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 11(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297448(CHEMBL564916 | N-(2-aminophenyl)-7,7-di(1H-indol-3...)copy SMILEScopy InChI
Affinity DataIC50: 5.80E+3nMAssay Description:Inhibition of human HDAC11 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297448(CHEMBL564916 | N-(2-aminophenyl)-7,7-di(1H-indol-3...)copy SMILEScopy InChI
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of human HDAC1 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297448(CHEMBL564916 | N-(2-aminophenyl)-7,7-di(1H-indol-3...)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+4nMAssay Description:Inhibition of human HDAC5 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297448(CHEMBL564916 | N-(2-aminophenyl)-7,7-di(1H-indol-3...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of human HDAC9 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297448(CHEMBL564916 | N-(2-aminophenyl)-7,7-di(1H-indol-3...)copy SMILEScopy InChI
Affinity DataIC50: 7.30E+4nMAssay Description:Inhibition of human HDAC10 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Sigma-Tau Research and Development

Curated by ChEMBL
LigandPNGBDBM50297448(CHEMBL564916 | N-(2-aminophenyl)-7,7-di(1H-indol-3...)copy SMILEScopy InChI
Affinity DataIC50: 7.40E+4nMAssay Description:Inhibition of human HDAC8 by fluroimetryChecked by AuthorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PN95PTPubMed
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