Compile Data Set for Download or QSAR
Found 46 with Last Name = 'bouchet' and Initial = 's'
TargetHistone deacetylase 3(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525406(CHEMBL164868)copy SMILEScopy InChI
Affinity DataIC50: 10nMAssay Description:Inhibition of human recombinant HDAC3 using fluorogenic HDAC substrate measured after 10 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525406(CHEMBL164868)copy SMILEScopy InChI
Affinity DataIC50: 11nMAssay Description:Inhibition of human recombinant HDAC1 using fluorogenic HDAC substrate measured after 15 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525406(CHEMBL164868)copy SMILEScopy InChI
Affinity DataIC50: 16nMAssay Description:Inhibition of human recombinant HDAC2 using fluorogenic HDAC substrate measured after 15 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525406(CHEMBL164868)copy SMILEScopy InChI
Affinity DataIC50: 22nMAssay Description:Inhibition of human recombinant HDAC6 using fluorogenic HDAC substrate measured after 30 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525406(CHEMBL164868)copy SMILEScopy InChI
Affinity DataIC50: 40nMAssay Description:Inhibition of human recombinant HDAC10 using fluorogenic HDAC substrate measured after 45 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 50nMAssay Description:Inhibition of HDAC6 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMedDrugBank
TargetHistone deacetylase 6(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525404(CHEMBL4563988)copy SMILEScopy InChI
Affinity DataIC50: 95nMAssay Description:Inhibition of human recombinant HDAC6 using fluorogenic HDAC substrate measured after 30 mins by fluorimetry assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 140nMAssay Description:Inhibition of HDAC3 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMedDrugBank
TargetHistone deacetylase 1(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 350nMAssay Description:Inhibition of HDAC1 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
TargetHistone deacetylase 2(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataIC50: 550nMAssay Description:Inhibition of HDAC2 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
TargetHistone deacetylase 8(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525406(CHEMBL164868)copy SMILEScopy InChI
Affinity DataIC50: 790nMAssay Description:Inhibition of human recombinant HDAC8 using fluorogenic HDAC substrate measured after 60 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 7(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525406(CHEMBL164868)copy SMILEScopy InChI
Affinity DataIC50: 980nMAssay Description:Inhibition of human recombinant HDAC7 using fluorogenic HDAC substrate class 2a measured after 45 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525404(CHEMBL4563988)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibition of human recombinant HDAC3 using fluorogenic HDAC substrate measured after 10 mins by fluorimetry assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetPolyamine deacetylase HDAC10(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525404(CHEMBL4563988)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of human recombinant HDAC10 using fluorogenic HDAC substrate measured after 45 mins by fluorimetry assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 8(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525404(CHEMBL4563988)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of human recombinant HDAC8 using fluorogenic HDAC substrate measured after 60 mins by fluorimetry assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 5(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525406(CHEMBL164868)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+3nMAssay Description:Inhibition of human recombinant HDAC5 using fluorogenic HDAC substrate class 2a measured after 30 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50115661(CHEMBL320497 | N,8-dihydroxy-8-(hydroxyamino)octan...)copy SMILEScopy InChI
Affinity DataIC50: 2.03E+3nMAssay Description:Inhibition of HDAC6 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 4(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525406(CHEMBL164868)copy SMILEScopy InChI
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of human recombinant HDAC4 using fluorogenic HDAC substrate class 2a measured after 30 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50499957(CHEMBL3739529)copy SMILEScopy InChI
Affinity DataIC50: 3.39E+3nMAssay Description:Inhibition of HDAC6 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525404(CHEMBL4563988)copy SMILEScopy InChI
Affinity DataIC50: 3.40E+3nMAssay Description:Inhibition of human recombinant HDAC2 using fluorogenic HDAC substrate measured after 15 mins by fluorimetry assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525404(CHEMBL4563988)copy SMILEScopy InChI
Affinity DataIC50: 3.50E+3nMAssay Description:Inhibition of human recombinant HDAC1 using fluorogenic HDAC substrate measured after 15 mins by fluorimetry assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM19422(4-(acetylamino)-N-(2-amino-phenyl) benzamide | CI-...)copy SMILEScopy InChI
Affinity DataIC50: 3.85E+3nMAssay Description:Inhibition of HDAC2 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 9(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525406(CHEMBL164868)copy SMILEScopy InChI
Affinity DataIC50: 5.10E+3nMAssay Description:Inhibition of human recombinant HDAC9 using fluorogenic HDAC substrate class 2a measured after 30 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 11(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50328678(6-(1,3-Dioxo-1H,3H-benzo[de]isoquinolin-2-yl)-hexa...)copy SMILEScopy InChI
Affinity DataIC50: 5.20E+3nMAssay Description:Inhibition of human recombinant HDAC11 using fluorogenic HDAC substrate class 2a measured after 30 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50115661(CHEMBL320497 | N,8-dihydroxy-8-(hydroxyamino)octan...)copy SMILEScopy InChI
Affinity DataIC50: 6.31E+3nMAssay Description:Inhibition of HDAC1 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 11(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525404(CHEMBL4563988)copy SMILEScopy InChI
Affinity DataIC50: 6.60E+3nMAssay Description:Inhibition of human recombinant HDAC11 using fluorogenic HDAC substrate class 2a measured after 30 mins by fluorimetry assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetNAD-dependent protein deacetylase sirtuin-1(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50179360(CHEMBL3040216)copy SMILEScopy InChI
Affinity DataIC50: 6.70E+3nMAssay Description:Inhibition of human recombinant sirtuin 1 using fluorogenic HDAC substrate measured after 20 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50115661(CHEMBL320497 | N,8-dihydroxy-8-(hydroxyamino)octan...)copy SMILEScopy InChI
Affinity DataIC50: 8.23E+3nMAssay Description:Inhibition of HDAC2 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetNAD-dependent protein deacetylase sirtuin-2(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50179360(CHEMBL3040216)copy SMILEScopy InChI
Affinity DataIC50: 1.70E+4nMAssay Description:Inhibition of human recombinant sirtuin 2 using fluoro-lysine sirtuin 2 deacetylase substrate measured after 60 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM19422(4-(acetylamino)-N-(2-amino-phenyl) benzamide | CI-...)copy SMILEScopy InChI
Affinity DataIC50: 1.82E+4nMAssay Description:Inhibition of HDAC1 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 2(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50499957(CHEMBL3739529)copy SMILEScopy InChI
Affinity DataIC50: 2.99E+4nMAssay Description:Inhibition of HDAC2 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 1(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50499957(CHEMBL3739529)copy SMILEScopy InChI
Affinity DataIC50: 3.06E+4nMAssay Description:Inhibition of HDAC1 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetNAD-dependent protein deacetylase sirtuin-3, mitochondrial(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM27507(3-Pyridinecarboxamide | CHEMBL1140 | NAM | niacina...)copy SMILEScopy InChI
Affinity DataIC50: 3.60E+4nMAssay Description:Inhibition of human recombinant sirtuin 3 using fluoro-lysine sirtuin 2 deacetylase substrate measured after 45 mins by fluorimetry assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50115661(CHEMBL320497 | N,8-dihydroxy-8-(hydroxyamino)octan...)copy SMILEScopy InChI
Affinity DataIC50: 6.26E+4nMAssay Description:Inhibition of HDAC3 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM19422(4-(acetylamino)-N-(2-amino-phenyl) benzamide | CI-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of HDAC6 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM19422(4-(acetylamino)-N-(2-amino-phenyl) benzamide | CI-...)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of HDAC3 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 3(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50499957(CHEMBL3739529)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of HDAC3 (unknown origin) by fluorimetric assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataEC50:  22nMAssay Description:Inhibition of HDAC6 in human HeLa cells assessed as inhibition of tubulin deacetylation incubated for overnight by cELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMedDrugBank
TargetHistone deacetylase(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)copy SMILEScopy InChI
Affinity DataEC50:  1.68E+3nMAssay Description:Inhibition of HDAC in human MeT-5A cells assessed as increase in transfected YFP fused histone H3 acetylation treated at 8 hrs after YFP fused H3 tra...More data for this Ligand-Target Pair
TargetHistone deacetylase 6(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50499957(CHEMBL3739529)copy SMILEScopy InChI
Affinity DataEC50:  5.00E+3nMAssay Description:Inhibition of HDAC6 in human HeLa cells assessed as inhibition of tubulin deacetylation incubated for overnight by cELISAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50499958(CHEMBL3740591)copy SMILEScopy InChI
Affinity DataEC50:  1.77E+4nMAssay Description:Inhibition of HDAC6 in human HeLa cells assessed as inhibition of tubulin deacetylation incubated for overnight by cELISAMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50115661(CHEMBL320497 | N,8-dihydroxy-8-(hydroxyamino)octan...)copy SMILEScopy InChI
Affinity DataEC50:  1.10E+3nMAssay Description:Inhibition of HDAC6 in human HeLa cells assessed as inhibition of tubulin deacetylation incubated for overnight by cELISAMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BK1GCPPubMed
TargetHistone deacetylase 6(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50005711(CHEBI:46024 | GNF-Pf-1011 | TRICHOSTATIN | Trichos...)copy SMILEScopy InChI
Affinity DataEC50:  5.20nMAssay Description:Inhibition of HDAC6 in human HeLa cells assessed as inhibition of tubulin deacetylation incubated for overnight by cELISAMore data for this Ligand-Target Pair
TargetHistone deacetylase(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525404(CHEMBL4563988)copy SMILEScopy InChI
Affinity DataEC50:  7.84E+3nMAssay Description:Inhibition of HDAC in human MeT-5A cells assessed as increase in transfected YFP fused histone H3 acetylation treated at 8 hrs after YFP fused H3 tra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM50525405(CHEMBL4516678)copy SMILEScopy InChI
Affinity DataEC50:  8.14E+3nMAssay Description:Inhibition of HDAC in human MeT-5A cells assessed as increase in transfected YFP fused histone H3 acetylation treated at 8 hrs after YFP fused H3 tra...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed
TargetHistone deacetylase(Homo sapiens (Human))
UMR CNRS 7285

Curated by ChEMBL
LigandPNGBDBM19422(4-(acetylamino)-N-(2-amino-phenyl) benzamide | CI-...)copy SMILEScopy InChI
Affinity DataEC50:  3.81E+3nMAssay Description:Inhibition of HDAC in human MeT-5A cells assessed as increase in transfected YFP fused histone H3 acetylation treated at 8 hrs after YFP fused H3 tra...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q23J3HDSPubMed