Compile Data Set for Download or QSAR
Found 42 with Last Name = 'hwang' and Initial = 'jh'
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM4367((3Z)-2-amino-3-[(3,4,5-trihydroxyphenyl)methyliden...)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibitory activity against PDGFRbeta kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178490(7,12-dioxo-5-(2-piperidin-1-yl-ethoxy)-7,12-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 2.80E+3nMAssay Description:Inhibitory activity against EGFR kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM4367((3Z)-2-amino-3-[(3,4,5-trihydroxyphenyl)methyliden...)copy SMILEScopy InChI
Affinity DataIC50: 4.10E+3nMAssay Description:Inhibitory activity against EGFR kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM4367((3Z)-2-amino-3-[(3,4,5-trihydroxyphenyl)methyliden...)copy SMILEScopy InChI
Affinity DataIC50: 4.30E+3nMAssay Description:Inhibitory activity against VEGFR2 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178490(7,12-dioxo-5-(2-piperidin-1-yl-ethoxy)-7,12-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 4.60E+3nMAssay Description:Inhibitory activity against VEGFR2 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM4367((3Z)-2-amino-3-[(3,4,5-trihydroxyphenyl)methyliden...)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibitory activity against FGFR1 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178494(5-(2-diethylamino-ethoxy)-7,12-dioxo-7,12-dihydro-...)copy SMILEScopy InChI
Affinity DataIC50: 5.10E+3nMAssay Description:Inhibitory activity against EGFR kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178492(7,12-dioxo-5-(2-pyrrolidin-1-yl-ethoxy)-7,12-dihyd...)copy SMILEScopy InChI
Affinity DataIC50: 5.50E+3nMAssay Description:Inhibitory activity against VEGFR2 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178490(7,12-dioxo-5-(2-piperidin-1-yl-ethoxy)-7,12-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 5.50E+3nMAssay Description:Inhibitory activity against PDGFRbeta kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178490(7,12-dioxo-5-(2-piperidin-1-yl-ethoxy)-7,12-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 7.10E+3nMAssay Description:Inhibitory activity against FGFR1 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178495(5-(2-dimethylamino-ethoxy)-7,12-dioxo-7,12-dihydro...)copy SMILEScopy InChI
Affinity DataIC50: 7.60E+3nMAssay Description:Inhibitory activity against PDGFRbeta kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178492(7,12-dioxo-5-(2-pyrrolidin-1-yl-ethoxy)-7,12-dihyd...)copy SMILEScopy InChI
Affinity DataIC50: 8.70E+3nMAssay Description:Inhibitory activity against PDGFRbeta kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178494(5-(2-diethylamino-ethoxy)-7,12-dioxo-7,12-dihydro-...)copy SMILEScopy InChI
Affinity DataIC50: 8.80E+3nMAssay Description:Inhibitory activity against FGFR1 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178492(7,12-dioxo-5-(2-pyrrolidin-1-yl-ethoxy)-7,12-dihyd...)copy SMILEScopy InChI
Affinity DataIC50: 9.00E+3nMAssay Description:Inhibitory activity against EGFR kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178491(5-(3-dimethylamino-propoxy)-7,12-dioxo-7,12-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 1.02E+4nMAssay Description:Inhibitory activity against PDGFRbeta kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178494(5-(2-diethylamino-ethoxy)-7,12-dioxo-7,12-dihydro-...)copy SMILEScopy InChI
Affinity DataIC50: 1.26E+4nMAssay Description:Inhibitory activity against VEGFR2 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178493(5-methoxy-7,12-dioxo-7,12-dihydro-dinaphtho[1,2-b;...)copy SMILEScopy InChI
Affinity DataIC50: 1.26E+4nMAssay Description:Inhibitory activity against EGFR kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178495(5-(2-dimethylamino-ethoxy)-7,12-dioxo-7,12-dihydro...)copy SMILEScopy InChI
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibitory activity against VEGFR2 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178491(5-(3-dimethylamino-propoxy)-7,12-dioxo-7,12-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 1.36E+4nMAssay Description:Inhibitory activity against EGFR kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetVascular endothelial growth factor receptor 2(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178491(5-(3-dimethylamino-propoxy)-7,12-dioxo-7,12-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 1.55E+4nMAssay Description:Inhibitory activity against VEGFR2 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178494(5-(2-diethylamino-ethoxy)-7,12-dioxo-7,12-dihydro-...)copy SMILEScopy InChI
Affinity DataIC50: 1.59E+4nMAssay Description:Inhibitory activity against PDGFRbeta kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetTyrosyl-DNA phosphodiesterase 1(Homo sapiens (Human))
Biomedicinal Information Research Center (BIRC)

Curated by ChEMBL
LigandPNGBDBM50384889(CHEMBL2036061)copy SMILEScopy InChI
Affinity DataIC50: 1.80E+4nMAssay Description:Inhibition of human Tdp1 using 3'-phosphate-(4-methylumbelliferone)-thymidine as substrate after 180 mins by spectrophotometryMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2V9893KPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178495(5-(2-dimethylamino-ethoxy)-7,12-dioxo-7,12-dihydro...)copy SMILEScopy InChI
Affinity DataIC50: 2.36E+4nMAssay Description:Inhibitory activity against FGFR1 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178492(7,12-dioxo-5-(2-pyrrolidin-1-yl-ethoxy)-7,12-dihyd...)copy SMILEScopy InChI
Affinity DataIC50: 2.38E+4nMAssay Description:Inhibitory activity against FGFR1 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178495(5-(2-dimethylamino-ethoxy)-7,12-dioxo-7,12-dihydro...)copy SMILEScopy InChI
Affinity DataIC50: 3.10E+4nMAssay Description:Inhibitory activity against EGFR kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178491(5-(3-dimethylamino-propoxy)-7,12-dioxo-7,12-dihydr...)copy SMILEScopy InChI
Affinity DataIC50: 3.84E+4nMAssay Description:Inhibitory activity against FGFR1 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178496(7,12-dioxo-5-propoxy-7,12-dihydro-dinaphtho[1,2-b;...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibitory activity against EGFR kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178493(5-methoxy-7,12-dioxo-7,12-dihydro-dinaphtho[1,2-b;...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibitory activity against PDGFRbeta kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178493(5-methoxy-7,12-dioxo-7,12-dihydro-dinaphtho[1,2-b;...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibitory activity against FGFR1 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetFibroblast growth factor receptor 1(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178496(7,12-dioxo-5-propoxy-7,12-dihydro-dinaphtho[1,2-b;...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibitory activity against FGFR1 kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetPlatelet-derived growth factor receptor beta(Homo sapiens (Human))
Korea Research Institute of Chemical Technology

Curated by ChEMBL
LigandPNGBDBM50178496(7,12-dioxo-5-propoxy-7,12-dihydro-dinaphtho[1,2-b;...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibitory activity against PDGFRbeta kinaseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2SF2VQRPubMed
TargetAmine oxidase [flavin-containing] A(Mus musculus)
Chungbuk National University

Curated by ChEMBL
LigandPNGBDBM50193718(2-(2,4-dihydroxy-phenyl)-5-hydroxy-8,8-dimethyl-3-...)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+4nMAssay Description:Inhibition at monoamine oxidase in mouse brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K938CCPubMed
TargetAmine oxidase [flavin-containing] A(Mus musculus)
Chungbuk National University

Curated by ChEMBL
LigandPNGBDBM50175016(1,3,6,7-tetrahydroxy-4-(1,1-dimethyl-2-propenyl)-8...)copy SMILEScopy InChI
Affinity DataIC50: 8.83E+4nMAssay Description:Inhibition at monoamine oxidase in mouse brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K938CCPubMed
TargetAmine oxidase [flavin-containing] A(Mus musculus)
Chungbuk National University

Curated by ChEMBL
LigandPNGBDBM50193719((S)-5,7,7'-trihydroxy-2',2'-dimethyl-6-(3-methylbu...)copy SMILEScopy InChI
Affinity DataIC50: 8.97E+4nMAssay Description:Inhibition at monoamine oxidase in mouse brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K938CCPubMed
TargetAmine oxidase [flavin-containing] A(Mus musculus)
Chungbuk National University

Curated by ChEMBL
LigandPNGBDBM50217268(1,6,7-trihydroxy-3-methoxy-2,4-(3-methylbut-2-enyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibition at monoamine oxidase in mouse brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K938CCPubMed
TargetAmine oxidase [flavin-containing] A(Mus musculus)
Chungbuk National University

Curated by ChEMBL
LigandPNGBDBM50217273(CHEMBL390040 | isocudraxanthone K)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibition at monoamine oxidase in mouse brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K938CCPubMed
TargetAmine oxidase [flavin-containing] A(Mus musculus)
Chungbuk National University

Curated by ChEMBL
LigandPNGBDBM50217274((-)-Cudraflavone A | 3,8-Dihydroxy-11,11-dimethyl-...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibition at monoamine oxidase in mouse brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K938CCPubMed
TargetAmine oxidase [flavin-containing] A(Mus musculus)
Chungbuk National University

Curated by ChEMBL
LigandPNGBDBM50175013(1,3,6,7-tetrahydroxy-5-(3-methylbut-2-enyl)-2-(2-m...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibition at monoamine oxidase in mouse brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K938CCPubMed
TargetAmine oxidase [flavin-containing] A(Mus musculus)
Chungbuk National University

Curated by ChEMBL
LigandPNGBDBM50175017(3,6,8-trihydroxy-2-methoxy-1-(3-methylbut-2-enyl)-...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibition at monoamine oxidase in mouse brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K938CCPubMed
TargetAmine oxidase [flavin-containing] A(Mus musculus)
Chungbuk National University

Curated by ChEMBL
LigandPNGBDBM50217270(1,3,6,7-tetrahydroxy-4-(1,1-dimethylallyl)xanthone...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibition at monoamine oxidase in mouse brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K938CCPubMed
TargetAmine oxidase [flavin-containing] A(Mus musculus)
Chungbuk National University

Curated by ChEMBL
LigandPNGBDBM50217269(1,3,6,7-tetrahydroxy-4-(1,1-dimethylallyl)-8-(3-hy...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibition at monoamine oxidase in mouse brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K938CCPubMed
TargetAmine oxidase [flavin-containing] A(Mus musculus)
Chungbuk National University

Curated by ChEMBL
LigandPNGBDBM50217272(1,6,7-trihydroxy-8-(3-methylbut-2-enyl)-4',5'-dihy...)copy SMILEScopy InChI
Affinity DataIC50: 1.50E+5nMAssay Description:Inhibition at monoamine oxidase in mouse brainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2K938CCPubMed