null

SMILES ONC(=O)\C=C\c1ccc(cc1)C(c1c[nH]c2ccccc12)c1c[nH]c2ccccc12

InChI Key InChIKey=WOXWAGCBPDSRPN-SDNWHVSQSA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 11 hits for monomerid = 50297447   

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 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 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 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 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
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
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
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
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
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 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