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Found 97 with Last Name = 'joe' and Initial = 'by'
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332481((R)-2-((R)-3-amino-3-(4-((2-methylquinolin-4-yl)me...)
Affinity DataIC50:  0.100nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332481((R)-2-((R)-3-amino-3-(4-((2-methylquinolin-4-yl)me...)
Affinity DataIC50:  0.100nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332476(2-((6-Methyl-2-oxo-2H-chromen-3-yl)methyl)-5-(3-(2...)
Affinity DataIC50:  0.270nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332476(2-((6-Methyl-2-oxo-2H-chromen-3-yl)methyl)-5-(3-(2...)
Affinity DataIC50:  0.270nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332480(4-(4-(2-(Diethylamino)ethoxy)phenyl)-2-((7-methyl-...)
Affinity DataIC50:  0.280nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332470(CHEMBL1630100 | N-Hydroxy-4-(4-hydroxyphenyl)-2-((...)
Affinity DataIC50:  0.300nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332479(4-(4-(2-(Diethylamino)ethoxy)phenyl)-2-((7-fluoro-...)
Affinity DataIC50:  0.460nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224961(2-benzyl-N-hydroxy-3-(6-methyl-2-oxo-2H-chromen-3-...)
Affinity DataIC50:  0.5nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332478(4-(4-(2-(Diethylamino)ethoxy)phenyl)-2-((6-methyl-...)
Affinity DataIC50:  0.530nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332477(4-(4-(2-(Dimethylamino)ethoxy)phenyl)-2-((6-methyl...)
Affinity DataIC50:  0.660nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332477(4-(4-(2-(Dimethylamino)ethoxy)phenyl)-2-((6-methyl...)
Affinity DataIC50:  0.660nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332474(2-((6-Methyl-2-oxo-2H-chromen-3-yl)methyl)-4-(3-(2...)
Affinity DataIC50:  0.900nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332473(2-((6-Methyl-2-oxo-2H-chromen-3-yl)methyl)-4-(4-(2...)
Affinity DataIC50:  1nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332472(3-(6-Methyl-2-oxo-2H-chromen-3-yl)-2-(3-(2-(piperi...)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332475(2-((6-Methyl-2-oxo-2H-chromen-3-yl)methyl)-5-(4-(2...)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224956(CHEMBL253710 | N-hydroxy-2-methyl-3-(6-methyl-2-ox...)
Affinity DataIC50:  3nMAssay Description:Inhibition of human TACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224961(2-benzyl-N-hydroxy-3-(6-methyl-2-oxo-2H-chromen-3-...)
Affinity DataIC50:  5nMAssay Description:Inhibition of human TACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target72 kDa type IV collagenase(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224959(3-(5-(hexa-2,4-dienylidene)-2-oxo-5,6-dihydro-2H-p...)
Affinity DataIC50:  6nMAssay Description:Inhibition of human recombinant MMP2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332471(3-(6-Methyl-2-oxo-2H-chromen-3-yl)-2-(4-(2-(piperi...)
Affinity DataIC50:  11nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314497(9-(1-ethylpyrrolidin-3-yloxy)-4,6-dihydro-1H-thiop...)
Affinity DataIC50:  13nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224959(3-(5-(hexa-2,4-dienylidene)-2-oxo-5,6-dihydro-2H-p...)
Affinity DataIC50:  23nMAssay Description:Inhibition of human recombinant MMP9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314494(9-(1-ethylpiperidin-3-yloxy)-4,6-dihydro-1H-thiopy...)
Affinity DataIC50:  25nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314492(9-(piperidin-3-yloxy)-4,6-dihydro-1H-thiopyrano[3,...)
Affinity DataIC50:  28nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224959(3-(5-(hexa-2,4-dienylidene)-2-oxo-5,6-dihydro-2H-p...)
Affinity DataIC50:  28nMAssay Description:Inhibition of human TACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314485(9-(1-(2-hydroxyethyl)piperidin-4-yloxy)-4,6-dihydr...)
Affinity DataIC50:  29nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224960(2-(6-methyl-2-oxo-2H-chromen-3-ylmethyl)-pent-4-en...)
Affinity DataIC50:  30nMAssay Description:Inhibition of human TACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332482(2-((6-Methyl-2-oxo-2H-chromen-3-yl)methyl)-6-pheny...)
Affinity DataIC50:  33nMAssay Description:Inhibition of human TACE by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224954(CHEMBL252693 | N-hydroxy-2-((6-methoxy-2H-chromen-...)
Affinity DataIC50:  36nMAssay Description:Inhibition of human TACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314490(9-(1-phenethylpiperidin-4-yloxy)-4,6-dihydro-1H-th...)
Affinity DataIC50:  38nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314493(9-(1-methylpiperidin-3-yloxy)-4,6-dihydro-1H-thiop...)
Affinity DataIC50:  39nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314486(9-(1-(2-methoxyethyl)piperidin-4-yloxy)-4,6-dihydr...)
Affinity DataIC50:  40nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM27525(N-[3-(morpholin-4-yl)propyl]-8-oxo-9-azatetracyclo...)
Affinity DataIC50:  40nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314482(9-(1-propylpiperidin-4-yloxy)-4,6-dihydro-1H-thiop...)
Affinity DataIC50:  42nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314483(9-(1-pentylpiperidin-4-yloxy)-4,6-dihydro-1H-thiop...)
Affinity DataIC50:  45nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314489(9-(1-benzylpiperidin-4-yloxy)-4,6-dihydro-1H-thiop...)
Affinity DataIC50:  53nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314495(9-(1-propylpiperidin-3-yloxy)-4,6-dihydro-1H-thiop...)
Affinity DataIC50:  56nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332480(4-(4-(2-(Diethylamino)ethoxy)phenyl)-2-((7-methyl-...)
Affinity DataIC50:  60nMAssay Description:Inhibition of human TNF-alpha by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224958(CHEMBL253489 | N-hydroxy-3-(6-methyl-2-oxo-2H-chro...)
Affinity DataIC50:  60nMAssay Description:Inhibition of human TACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetInhibitor of nuclear factor kappa-B kinase subunit beta(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50135482(1-(5-Methoxy-2-thiophen-2-yl-quinazolin-4-ylamino)...)
Affinity DataIC50:  62nMAssay Description:Inhibition of IKKbeta kinase (unknown origin) by Lance ULight systemMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50018492(CHEMBL3290626)
Affinity DataIC50:  65nMAssay Description:Inhibition of FLT3 kinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332479(4-(4-(2-(Diethylamino)ethoxy)phenyl)-2-((7-fluoro-...)
Affinity DataIC50:  70nMAssay Description:Inhibition of human TNF-alpha by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314484(9-(1-isopentylpiperidin-4-yloxy)-4,6-dihydro-1H-th...)
Affinity DataIC50:  71nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314496(9-(1-methylpyrrolidin-3-yloxy)-4,6-dihydro-1H-thio...)
Affinity DataIC50:  80nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50018490(CHEMBL3290634)
Affinity DataIC50:  85nMAssay Description:Inhibition of FLT3 kinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPoly [ADP-ribose] polymerase 1(Homo sapiens (Human))
Jeil Pharmaceutical

Curated by ChEMBL
LigandPNGBDBM50314481(9-hydroxy-4,6-dihydro-1H-thiopyrano[3,4-c]quinolin...)
Affinity DataIC50:  99nMAssay Description:Inhibition of PARP1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM13535(4-[6-methoxy-7-(3-piperidin-1-ylpropoxy)quinazolin...)
Affinity DataIC50:  102nMAssay Description:Inhibition of FLT3 kinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224955(CHEMBL402990 | N-hydroxy-3-(6-methoxy-2-oxo-2H-chr...)
Affinity DataIC50:  110nMAssay Description:Inhibition of human TACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50300690(1-(5-Tert-Butyl-1,2-Oxazol-3-Yl)-3-(4-{7-[2-(Morph...)
Affinity DataIC50:  120nMAssay Description:Inhibition of FLT3 kinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetReceptor-type tyrosine-protein kinase FLT3(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50018499(CHEMBL3290631)
Affinity DataIC50:  133nMAssay Description:Inhibition of FLT3 kinase (unknown origin)More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50332478(4-(4-(2-(Diethylamino)ethoxy)phenyl)-2-((6-methyl-...)
Affinity DataIC50:  140nMAssay Description:Inhibition of human TNF-alpha by fluorescent spectroscopyMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
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