BDBM50470579 4sc-202::Domatinostat
SMILES Cn1cc(cn1)-c1ccc(cc1)S(=O)(=O)n1ccc(\C=C\C(=O)Nc2ccccc2N)c1
InChI Key InChIKey=PRXXYMVLYKJITB-UHFFFAOYSA-N
Data 44 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 44 hits for monomerid = 50470579
TargetHistone deacetylase 1(Human)
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
Affinity DataIC50: 600nMAssay Description:Inhibition of LSD1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Human)
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of human recombinant HDAC1 using fluorogenic HDAC substrate incubated for 30 mins by fluorescence assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.12E+3nMAssay Description:Inhibition of human recombinant HDAC2 incubated for 60 mins by fluorescence based assayMore data for this Ligand-Target Pair
Affinity DataIC50: 570nMAssay Description:Inhibition of human recombinant HDAC3 incubated for 60 mins by fluorescence based assayMore data for this Ligand-Target Pair
Affinity DataIC50: 600nMAssay Description:Inhibition of human N-terminal His-tagged LSD1 using histone H3 peptide (1 to 21 residues) K4me2 as substrate preincubated for 30 mins followed by su...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Human)
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 1.12E+3nMAssay Description:Inhibition of HDAC2 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 570nMAssay Description:Inhibition of HDAC3 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 600nMAssay Description:Inhibition of human LSD1 (unknown orgin)More data for this Ligand-Target Pair
Affinity DataIC50: 9.70E+3nMAssay Description:Inhibition of HDAC11 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Human)
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
TargetHistone deacetylase 1(Human)
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of HDAC6 (unknown origin) using p53 residues (379 to 382)(RHKK(Ac)-AMC) as substrate by fluorescent methodMore data for this Ligand-Target Pair
TargetHistone deacetylase 1(Human)
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 600nMAssay Description:Inhibition of KDM1A/LSD1 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Human)
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of HDAC1 (unknown origin) using p53 residues (379 to 382)(RHKK(Ac)-AMC) as substrate by fluorescent methodMore data for this Ligand-Target Pair
Affinity DataIC50: 1.10E+3nMAssay Description:Inhibition of HDAC2 (unknown origin) using p53 residues (379 to 382)(RHKK(Ac)-AMC) as substrate by fluorescent methodMore data for this Ligand-Target Pair
Affinity DataIC50: 600nMAssay Description:Inhibition of HDAC3 (unknown origin) using p53 residues (379 to 382)(RHKK(Ac)-AMC) as substrate by fluorescent methodMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of HDAC8 (unknown origin) using p53 (379 to 382 residues)(RHK(Ac)K(ac)AMC) as substrate by fluorescent methodMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of HDAC4 (unknown origin) using HDAC class IIa substrate (trifluoroacetyl-lysine-AMC) as substrate by fluorescent methodMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of HDAC5 (unknown origin) using HDAC class IIa substrate (trifluoroacetyl-lysine-AMC) as substrate by fluorescent methodMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of HDAC7 (unknown origin) using HDAC class IIa substrate (trifluoroacetyl-lysine-AMC) as substrate by fluorescent methodMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of HDAC9 (unknown origin) using HDAC class IIa substrate (trifluoroacetyl-lysine-AMC) as substrate by fluorescent methodMore data for this Ligand-Target Pair
Affinity DataIC50: 130nMAssay Description:Inhibition of HDAC3 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of HDAC10 (unknown origin) using p53 residues (379 to 382)(RHKK(Ac)-AMC) as substrate by fluorescent methodMore data for this Ligand-Target Pair
Affinity DataIC50: 9.70E+3nMAssay Description:Inhibition of HDAC11 (unknown origin) using p53 (379 to 382 residues)(RHKK(Ac)-AMC) as substrate by fluorescent methodMore data for this Ligand-Target Pair
TargetHistone deacetylase 1(Human)
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
Affinity DataIC50: 0.160nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 370nMAssay Description:Inhibition of HDAC2 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 130nMAssay Description:Inhibition of HDAC3 (unknown origin)More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Human)
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
First Affiliated Hospital of Gannan Medical University
Curated by ChEMBL
Affinity DataIC50: 1.20E+3nMAssay Description:Inhibition of HDAC1 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 1.12E+3nMAssay Description:Inhibition of HDAC2 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 570nMAssay Description:Inhibition of HDAC3 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of HDAC9 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 2.10E+4nMAssay Description:Inhibition of HDAC10 (unknown origin)More data for this Ligand-Target Pair
