null

SMILES CNC(=O)C(CCCCCCNC(=O)c1cc(on1)-c1ccc(N)cc1)N=O

InChI Key InChIKey=LUOBQTLGSXROBD-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 = 50341840   

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

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)copy SMILEScopy InChI
Affinity DataIC50: 1.53E+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 3(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)copy SMILEScopy InChI
Affinity DataIC50: 4.44E+3nMAssay 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 11(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)copy SMILEScopy InChI
Affinity DataIC50: 2.81E+4nMAssay 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 1(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)copy SMILEScopy InChI
Affinity DataIC50: 1.16E+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
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)copy SMILEScopy InChI
Affinity DataIC50: 4.81E+4nMAssay 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
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)copy SMILEScopy InChI
Affinity DataIC50: 2.18E+4nMAssay 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
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)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
TargetHistone deacetylase 7(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)copy SMILEScopy InChI
Affinity DataIC50: 1.65E+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
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay 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
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+3nMAssay 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
TargetHistone deacetylase 4(Homo sapiens (Human))
Universita` degli Studi di Siena

Curated by ChEMBL
LigandPNGBDBM50341840(5-(4-Aminophenyl)-N-(7-(hydroxyimino)-8-(methylami...)copy SMILEScopy InChI
Affinity DataIC50: 4.88E+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