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Compile Data Set for Download or QSAR
maximum 50k data
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
(change energy unit to
kcal/mol
)
Found
28
hits in this display
Target
Carbonic anhydrase 12
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
Ki: 9.51E+3nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase 12 catalytic domain preincubated for 15 mins prior to testing by phenol red based stopped-flow CO2...
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Target
Mandelate racemase
(Pseudomonas putida (g-Proteobacteria))
Dalhousie University
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
Ki: 1.20E+4nM
Assay Description:
Inhibition of mandelate racemase in Pseudomonas putida
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Target
Carbonic anhydrase 9
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
Ki: 4.59E+4nM
Assay Description:
Compound was tested for inhibitory constant of Gamma-amino-N-butyrate transaminase in pig brain at pH of 8.5 and 25 degree C
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Target
Carbonic anhydrase 1
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
Ki: 8.31E+4nM
Assay Description:
Inhibition of recombinant human carbonic anhydrase 1 preincubated for 15 mins prior to testing by phenol red based stopped-flow CO2 hydration assay
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Target
Carbonic anhydrase 2
(Homo sapiens (Human))
Universit£
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
Ki: 1.79E+5nM
Assay Description:
Compound was tested for inhibition of purine nucleoside phosphorylase using human erythro lysate
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Target
Histone deacetylase 6
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 115nM
T: 2°C
Assay Description:
Inhibition of HDAC6 (unknown origin) assessed as fluorescence intensity measured after 60 mins incubation at room temperature by trypsin-free microfl...
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Histone deacetylase 6
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 1.34E+3nM
Assay Description:
Inhibition of recombinant human full length N-terminal GST-tagged HDAC6 expressed in Sf9 insect cells using Fluor de Lys deacetylase or Fluor de Lys ...
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Histone deacetylase 8
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 1.92E+3nM
T: 2°C
Assay Description:
Inhibition of HDAC8 (unknown origin) assessed as fluorescence intensity measured after 60 mins incubation at room temperature by trypsin-free microfl...
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Target
Histone deacetylase 6
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 2.37E+3nM
Assay Description:
Inhibition of recombinant full length human N-terminal GST-tagged HDAC6 expressed in baculovirus infected sf9 insect cells pretreated with compound f...
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Target
Histone deacetylase 6
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 2.37E+3nM
Assay Description:
Inhibition of recombinant full length human N-terminal GST-tagged HDAC6 expressed in baculovirus infected sf9 insect cells pretreated with compound f...
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Target
Histone deacetylase 1
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 4.73E+3nM
T: 2°C
Assay Description:
Inhibition of HDAC1 (unknown origin) assessed as fluorescence intensity measured after 60 mins incubation at room temperature by trypsin-free microfl...
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Histone deacetylase 3
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 7.83E+3nM
T: 2°C
Assay Description:
Inhibition of HDAC3 (unknown origin) assessed as fluorescence intensity measured after 60 mins incubation at room temperature by trypsin-free microfl...
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Histone deacetylase 2
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 7.91E+3nM
T: 2°C
Assay Description:
Inhibition of HDAC2 (unknown origin) assessed as fluorescence intensity measured after 60 mins incubation at room temperature by trypsin-free microfl...
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Histone deacetylase 7
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 1.56E+4nM
T: 2°C
Assay Description:
Inhibition of HDAC7 (unknown origin) assessed as fluorescence intensity measured after 60 mins incubation at room temperature by trypsin-free microfl...
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Target
Indoleamine 2,3-dioxygenase 1
(Homo sapiens (Human))
Bryn Mawr College
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 1.60E+4nM
Assay Description:
Inhibition of recombinant human IDO1 assessed as reduction in kynurenine production using L-tryptophan as substrate after 60 mins by microplate reade...
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Target
Histone deacetylase 1
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 2.00E+4nM
Assay Description:
Inhibition of HDAC1
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Target
Histone deacetylase 1
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 2.00E+4nM
Assay Description:
Inhibition of human HDAC1 expressed in domain of SMRT
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Target
Histone deacetylase 1
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 2.54E+4nM
Assay Description:
Inhibition of recombinant human C-terminal His-tagged HDAC1 expressed in Sf9 insect cells using Fluor de Lys deacetylase or Fluor de Lys Green deacet...
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Histone deacetylase 5
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: >3.33E+4nM
T: 2°C
Assay Description:
Inhibition of HDAC5 (unknown origin) assessed as fluorescence intensity measured after 60 mins incubation at room temperature by trypsin-free microfl...
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Histone deacetylase 4
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: >3.33E+4nM
T: 2°C
Assay Description:
Inhibition of HDAC4 (unknown origin) assessed as fluorescence intensity measured after 60 mins incubation at room temperature by trypsin-free microfl...
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Histone deacetylase 9
(Homo sapiens (Human))
Broad Institute Of Mit And Harvard
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: >3.33E+4nM
T: 2°C
Assay Description:
Inhibition of HDAC9 (unknown origin) assessed as fluorescence intensity measured after 60 mins incubation at room temperature by trypsin-free microfl...
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Target
Histone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2)
(Homo sapiens (Human))
Preclinical R&D
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 7.16E+4nM
Assay Description:
Inhibition of C-terminal His-tagged human HDAC3 (1 to 428 residues)/N-terminal GST tagged human NCOR2 (395 to 489) expressed in baculovirus infected ...
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Target
Histone deacetylase 3/Nuclear receptor corepressor 2 (HDAC3/NCoR2)
(Homo sapiens (Human))
Preclinical R&D
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 7.16E+4nM
Assay Description:
Inhibition of C-terminal His-tagged human HDAC3 (1 to 428 residues)/N-terminal GST tagged human NCOR2 (395 to 489) expressed in baculovirus infected ...
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Target
Polyunsaturated fatty acid 5-lipoxygenase
(Rattus norvegicus)
TBA
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 1.10E+5nM
Assay Description:
In vitro inhibitory activity against RBL-1 5-LO
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Target
Polyunsaturated fatty acid 5-lipoxygenase
(Rattus norvegicus)
TBA
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 1.10E+5nM
Assay Description:
In vitro inhibitory activity against 5-lipoxygenase in rat basophilic leukemia cells(RBL-1)
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Target
Polyunsaturated fatty acid 5-lipoxygenase
(Rattus norvegicus)
TBA
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
IC50: 1.12E+5nM
Assay Description:
In vitro inhibitory activity against 5-lipoxygenase in rat basophilic leukemia cells(RBL-1)
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Target
Polymerase acidic protein
(Hepatitis C virus)
Roche Discovery Welwyn
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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IC50: >5.00E+5nM
Assay Description:
Inhibitory concentration against cap-dependent endonuclease activity of influenza virus RNP
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Target
Stromelysin-1
(Homo sapiens (Human))
Abbott Laboratories
Curated by
ChEMBL
Ligand
BDBM50015184
(BENZHYDROXAMIC ACID | BENZOHYDROXAMATE | CHEMBL163...)
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Affinity Data
Kd: 7.00E+6nM
Assay Description:
Binding to stromelysin (MMP-3) in place of acetohydroxamic acid.
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