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Found 45 with Last Name = 'chun' and Initial = 'tg'
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
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
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
TargetAdenosylhomocysteinase(Rattus norvegicus)
Boston College

Curated by ChEMBL
LigandPNGBDBM50316222(CHEMBL1095280 | D-ERITADENINE | eritadenine)
Affinity DataIC50:  30nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase in intact rat hepatocytesMore data for this Ligand-Target Pair
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
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
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
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM19149(CHEMBL98 | N-hydroxy-N'-phenyloctanediamide | SAHA...)
Affinity DataIC50:  110nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
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
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50476373(CHEMBL226224)
Affinity DataIC50:  130nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224963(CHEMBL252674 | N-hydroxy-3-(2-oxo-2H-chromen-3-yl)...)
Affinity DataIC50:  150nMAssay 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
LigandPNGBDBM50224963(CHEMBL252674 | N-hydroxy-3-(2-oxo-2H-chromen-3-yl)...)
Affinity DataIC50:  200nMAssay Description:Inhibition of human recombinant MMP2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target72 kDa type IV collagenase(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224958(CHEMBL253489 | N-hydroxy-3-(6-methyl-2-oxo-2H-chro...)
Affinity DataIC50:  230nMAssay Description:Inhibition of human recombinant MMP2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50476376(CHEMBL388174)
Affinity DataIC50:  270nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50475867(CHEMBL214049)
Affinity DataIC50:  350nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Boston College

Curated by ChEMBL
LigandPNGBDBM50316223(3-(6-Amino-purin-9-ylmethyl)-5-cyclohexylmethoxy-b...)
Affinity DataIC50:  400nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50475869(CHEMBL211802)
Affinity DataIC50:  500nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224962(3-(6-chloro-2-oxo-2H-chromen-3-yl)-N-hydroxy-propa...)
Affinity DataIC50:  550nMAssay 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
LigandPNGBDBM50224955(CHEMBL402990 | N-hydroxy-3-(6-methoxy-2-oxo-2H-chr...)
Affinity DataIC50:  590nMAssay Description:Inhibition of human recombinant MMP2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50475868(CHEMBL213997)
Affinity DataIC50:  670nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224957(3-(6-bromo-2-oxo-2H-chromen-3-yl)-N-hydroxy-propan...)
Affinity DataIC50:  840nMAssay 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
LigandPNGBDBM50224957(3-(6-bromo-2-oxo-2H-chromen-3-yl)-N-hydroxy-propan...)
Affinity DataIC50:  860nMAssay Description:Inhibition of human recombinant MMP2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Boston College

Curated by ChEMBL
LigandPNGBDBM50006222((1S,2R,5R)-5-(6-Amino-purin-9-yl)-3-hydroxymethyl-...)
Affinity DataIC50:  900nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target72 kDa type IV collagenase(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224956(CHEMBL253710 | N-hydroxy-2-methyl-3-(6-methyl-2-ox...)
Affinity DataIC50:  1.04E+3nMAssay Description:Inhibition of human recombinant MMP2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224963(CHEMBL252674 | N-hydroxy-3-(2-oxo-2H-chromen-3-yl)...)
Affinity DataIC50:  1.41E+3nMAssay Description:Inhibition of human recombinant MMP9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target72 kDa type IV collagenase(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224962(3-(6-chloro-2-oxo-2H-chromen-3-yl)-N-hydroxy-propa...)
Affinity DataIC50:  1.47E+3nMAssay Description:Inhibition of human recombinant MMP2More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224958(CHEMBL253489 | N-hydroxy-3-(6-methyl-2-oxo-2H-chro...)
Affinity DataIC50:  3.05E+3nMAssay Description:Inhibition of human recombinant MMP9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50476377(CHEMBL226229)
Affinity DataIC50:  3.21E+3nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50475866(CHEMBL213860)
Affinity DataIC50:  4.27E+3nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224955(CHEMBL402990 | N-hydroxy-3-(6-methoxy-2-oxo-2H-chr...)
Affinity DataIC50:  5.66E+3nMAssay Description:Inhibition of human recombinant MMP9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50476375(CHEMBL226172)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50476374(CHEMBL226173)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224956(CHEMBL253710 | N-hydroxy-2-methyl-3-(6-methyl-2-ox...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human recombinant MMP9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50476382(CHEMBL211090)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50476381(CHEMBL226174)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50476380(CHEMBL427448)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50476379(CHEMBL444888)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetHistone deacetylase(Homo sapiens (Human))
Kribb

Curated by ChEMBL
LigandPNGBDBM50476378(CHEMBL226230)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of HDAC in HeLa cells by fluorescent activity assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
TargetDisintegrin and metalloproteinase domain-containing protein 17(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224964(3-(6-tert-butyl-2-oxo-2H-chromen-3-yl)-N-hydroxypr...)
Affinity DataIC50:  1.24E+4nMAssay Description:Inhibition of human TACEMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224962(3-(6-chloro-2-oxo-2H-chromen-3-yl)-N-hydroxy-propa...)
Affinity DataIC50:  1.64E+4nMAssay Description:Inhibition of human recombinant MMP9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMatrix metalloproteinase-9(Homo sapiens (Human))
Yonsei University

Curated by ChEMBL
LigandPNGBDBM50224957(3-(6-bromo-2-oxo-2H-chromen-3-yl)-N-hydroxy-propan...)
Affinity DataIC50:  2.45E+4nMAssay Description:Inhibition of human recombinant MMP9More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Boston College

Curated by ChEMBL
LigandPNGBDBM50240866((-)-ilimaquinone | 2-Hydroxy-5-methoxy-3-((1R,2S,4...)
Affinity DataIC50:  4.00E+4nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenosylhomocysteinase(Homo sapiens (Human))
Boston College

Curated by ChEMBL
LigandPNGBDBM50316224((2R,4aS,5R,6S,8aS)-5-((2-chloro-5-methoxy-3,6-diox...)
Affinity DataIC50: >2.50E+5nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase after 10 mins by scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed