null

SMILES CNC(=O)C(CCCCCCC(=O)Nc1ccccc1)N=O

InChI Key InChIKey=LEVQYUXQSVPMMA-UHFFFAOYSA-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 = 50341844   

TargetHistone deacetylase 5(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)copy SMILEScopy InChI
Affinity DataIC50: 5.93E+4nMAssay Description:Inhibition of human HDAC5 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5TNZPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)copy SMILEScopy InChI
Affinity DataIC50: 5.67E+4nMAssay Description:Inhibition of human HDAC1 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5TNZPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human HDAC2 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5TNZPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)copy SMILEScopy InChI
Affinity DataIC50: 1.86E+4nMAssay Description:Inhibition of human HDAC3 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5TNZPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)copy SMILEScopy InChI
Affinity DataIC50: 6.57E+4nMAssay Description:Inhibition of human HDAC4 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5TNZPubMed
TargetHistone deacetylase 11(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human HDAC11 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5TNZPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)copy SMILEScopy InChI
Affinity DataIC50: 3.62E+4nMAssay Description:Inhibition of human HDAC7 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5TNZPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)copy SMILEScopy InChI
Affinity DataIC50: 2.26E+4nMAssay Description:Inhibition of human HDAC8 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5TNZPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)copy SMILEScopy InChI
Affinity DataIC50: 3.07E+4nMAssay Description:Inhibition of human HDAC9 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5TNZPubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human HDAC10 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5TNZPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341844(2-(Hydroxyimino)-N1-methyl-N9-phenylnonanediamide ...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of human HDAC6 using ArgHisLysLys(Ac) fluorogenic peptide as a substrate by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2CR5TNZPubMed