Compile Data Set for Download or QSAR
Found 54 with Last Name = 'maglathlin' and Initial = 'rl'
TargetHistone deacetylase 6(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50015142(4-Phenylbutyrohydroxamic acid | CHEMBL55895 | N-Hy...)copy SMILEScopy InChI
Affinity DataIC50: 500nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50015142(4-Phenylbutyrohydroxamic acid | CHEMBL55895 | N-Hy...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50015142(4-Phenylbutyrohydroxamic acid | CHEMBL55895 | N-Hy...)copy SMILEScopy InChI
Affinity DataIC50: 600nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336883(Butyrylhydroxamic acid | CHEMBL1672332)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50015142(4-Phenylbutyrohydroxamic acid | CHEMBL55895 | N-Hy...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+3nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50015142(4-Phenylbutyrohydroxamic acid | CHEMBL55895 | N-Hy...)copy SMILEScopy InChI
Affinity DataIC50: 4.00E+3nMAssay Description:Inhibition of human recombinant HDAC8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336883(Butyrylhydroxamic acid | CHEMBL1672332)copy SMILEScopy InChI
Affinity DataIC50: 7.00E+3nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 9.00E+3nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336883(Butyrylhydroxamic acid | CHEMBL1672332)copy SMILEScopy InChI
Affinity DataIC50: 9.00E+3nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336883(Butyrylhydroxamic acid | CHEMBL1672332)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 1.20E+4nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+4nMAssay Description:Inhibition of human recombinant HDAC8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | CHEMBL18631...)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50015142(4-Phenylbutyrohydroxamic acid | CHEMBL55895 | N-Hy...)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+4nMAssay Description:Inhibition of human recombinant HDAC5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336883(Butyrylhydroxamic acid | CHEMBL1672332)copy SMILEScopy InChI
Affinity DataIC50: 2.60E+4nMAssay Description:Inhibition of human recombinant HDAC8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | CHEMBL18631...)copy SMILEScopy InChI
Affinity DataIC50: 3.70E+4nMAssay Description:Inhibition of human recombinant HDAC5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50003616(2-n-propyl-n-valeric acid | CHEMBL109 | DPA | Di-n...)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+4nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | CHEMBL18631...)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+4nMAssay Description:Inhibition of human recombinant HDAC8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50003616(2-n-propyl-n-valeric acid | CHEMBL109 | DPA | Di-n...)copy SMILEScopy InChI
Affinity DataIC50: 6.20E+4nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMedDrugBank
TargetHistone deacetylase 1(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM36184(4-phenylbutanoate)copy SMILEScopy InChI
Affinity DataIC50: 6.40E+4nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM36184(4-phenylbutanoate)copy SMILEScopy InChI
Affinity DataIC50: 6.50E+4nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | CHEMBL18631...)copy SMILEScopy InChI
Affinity DataIC50: 9.10E+4nMAssay Description:Inhibition of human recombinant HDAC9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM36184(4-phenylbutanoate)copy SMILEScopy InChI
Affinity DataIC50: 9.30E+4nMAssay Description:Inhibition of human recombinant HDAC8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | CHEMBL18631...)copy SMILEScopy InChI
Affinity DataIC50: 9.90E+4nMAssay Description:Inhibition of human recombinant HDAC7More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50003616(2-n-propyl-n-valeric acid | CHEMBL109 | DPA | Di-n...)copy SMILEScopy InChI
Affinity DataIC50: 1.03E+5nMAssay Description:Inhibition of human recombinant HDAC8More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50015142(4-Phenylbutyrohydroxamic acid | CHEMBL55895 | N-Hy...)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+5nMAssay Description:Inhibition of human recombinant HDAC4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50015142(4-Phenylbutyrohydroxamic acid | CHEMBL55895 | N-Hy...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibition of human recombinant HDAC7More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50003616(2-n-propyl-n-valeric acid | CHEMBL109 | DPA | Di-n...)copy SMILEScopy InChI
Affinity DataIC50: 1.61E+5nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | CHEMBL18631...)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+5nMAssay Description:Inhibition of human recombinant HDAC4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM36184(4-phenylbutanoate)copy SMILEScopy InChI
Affinity DataIC50: 2.40E+5nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM36184(4-phenylbutanoate)copy SMILEScopy InChI
Affinity DataIC50: 2.60E+5nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | CHEMBL18631...)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+5nMAssay Description:Inhibition of human recombinant HDAC3More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336883(Butyrylhydroxamic acid | CHEMBL1672332)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+5nMAssay Description:Inhibition of human recombinant HDAC5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50015142(4-Phenylbutyrohydroxamic acid | CHEMBL55895 | N-Hy...)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+5nMAssay Description:Inhibition of human recombinant HDAC9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | CHEMBL18631...)copy SMILEScopy InChI
Affinity DataIC50: 5.60E+5nMAssay Description:Inhibition of human recombinant HDAC1More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336884(2-Propyl-pentanoic acid hydroxyamide | CHEMBL18631...)copy SMILEScopy InChI
Affinity DataIC50: 6.80E+5nMAssay Description:Inhibition of human recombinant HDAC2More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336883(Butyrylhydroxamic acid | CHEMBL1672332)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+6nMAssay Description:Inhibition of human recombinant HDAC7More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC7More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50003616(2-n-propyl-n-valeric acid | CHEMBL109 | DPA | Di-n...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50003616(2-n-propyl-n-valeric acid | CHEMBL109 | DPA | Di-n...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMedDrugBank
TargetHistone deacetylase 7(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50003616(2-n-propyl-n-valeric acid | CHEMBL109 | DPA | Di-n...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC7More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50003616(2-n-propyl-n-valeric acid | CHEMBL109 | DPA | Di-n...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC5More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50003616(2-n-propyl-n-valeric acid | CHEMBL109 | DPA | Di-n...)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM26109(Butyrate | butanoic acid | butanoic acid, 4)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC6More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336883(Butyrylhydroxamic acid | CHEMBL1672332)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC4More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
Broad Institute of Harvard and MIT

Curated by ChEMBL
LigandPNGBDBM50336883(Butyrylhydroxamic acid | CHEMBL1672332)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+6nMAssay Description:Inhibition of human recombinant HDAC9More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2TH8NQJPubMed
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