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Found 18 with Last Name = 'sing' and Initial = 'wt'
TargetPlasminogen(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096594(3-Allyl-5-[1-(6-nitro-benzo[1,3]dioxol-5-yl)-meth-...)
Affinity DataIC50: <1.00E+3nMAssay Description:Inhibitory activity of the compound against plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096592(CHEMBL369234 | {5-[1-(6-Nitro-benzo[1,3]dioxol-5-y...)
Affinity DataIC50: <1.00E+3nMAssay Description:Inhibitory activity of the compound against plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096596(CHEMBL425679 | {5-[1-Biphenyl-4-yl-eth-(Z)-ylidene...)
Affinity DataIC50:  7.00E+3nMAssay Description:Inhibitory activity of the compound against plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096591(CHEMBL366853 | {5-[1-(2-Fluoro-5-nitro-phenyl)-met...)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibitory activity of the compound against plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Hepatitis C virus)
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096593(CHEMBL369617 | {5-[1-{3-[4'-(2-tert-Butoxycarbonyl...)
Affinity DataIC50:  1.50E+4nMAssay Description:Inhibitory activity of the compound against hepatitis C virus (HCV) NS3 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Hepatitis C virus)
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096595(4-{[(2-{(4-Chloro-benzyl)-[2-(3-{1-[3-ethoxycarbon...)
Affinity DataIC50:  1.60E+4nMAssay Description:Inhibitory activity of the compound against hepatitis C virus (HCV) NS3 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096595(4-{[(2-{(4-Chloro-benzyl)-[2-(3-{1-[3-ethoxycarbon...)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibitory activity of the compound against plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Hepatitis C virus)
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096596(CHEMBL425679 | {5-[1-Biphenyl-4-yl-eth-(Z)-ylidene...)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibitory activity of the compound against hepatitis C virus (HCV) NS3 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPlasminogen(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096593(CHEMBL369617 | {5-[1-{3-[4'-(2-tert-Butoxycarbonyl...)
Affinity DataIC50:  2.00E+4nMAssay Description:Inhibitory activity of the compound against plasminMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096596(CHEMBL425679 | {5-[1-Biphenyl-4-yl-eth-(Z)-ylidene...)
Affinity DataIC50:  2.30E+4nMAssay Description:Inhibitory activity of the compound against Serine protease chymotrypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096594(3-Allyl-5-[1-(6-nitro-benzo[1,3]dioxol-5-yl)-meth-...)
Affinity DataIC50:  2.70E+4nMAssay Description:Inhibitory activity of the compound against Serine protease chymotrypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096592(CHEMBL369234 | {5-[1-(6-Nitro-benzo[1,3]dioxol-5-y...)
Affinity DataIC50:  3.80E+4nMAssay Description:Inhibitory activity of the compound against Serine protease chymotrypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Hepatitis C virus)
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096594(3-Allyl-5-[1-(6-nitro-benzo[1,3]dioxol-5-yl)-meth-...)
Affinity DataIC50:  4.00E+4nMAssay Description:Inhibitory activity of the compound against hepatitis C virus (HCV) NS3 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Hepatitis C virus)
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096591(CHEMBL366853 | {5-[1-(2-Fluoro-5-nitro-phenyl)-met...)
Affinity DataIC50:  6.40E+4nMAssay Description:Inhibitory activity of the compound against hepatitis C virus (HCV) NS3 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetGenome polyprotein(Hepatitis C virus)
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096592(CHEMBL369234 | {5-[1-(6-Nitro-benzo[1,3]dioxol-5-y...)
Affinity DataIC50:  7.10E+4nMAssay Description:Inhibitory activity of the compound against hepatitis C virus (HCV) NS3 proteaseMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096591(CHEMBL366853 | {5-[1-(2-Fluoro-5-nitro-phenyl)-met...)
Affinity DataIC50: >2.00E+5nMAssay Description:Inhibitory activity of the compound against Serine protease chymotrypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096595(4-{[(2-{(4-Chloro-benzyl)-[2-(3-{1-[3-ethoxycarbon...)
Affinity DataIC50:  2.10E+5nMAssay Description:Inhibitory activity of the compound against Serine protease chymotrypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetChymotrypsin-C(Homo sapiens (Human))
Institute Of Molecular And Cell Biology

Curated by ChEMBL
LigandPNGBDBM50096593(CHEMBL369617 | {5-[1-{3-[4'-(2-tert-Butoxycarbonyl...)
Affinity DataIC50:  3.75E+5nMAssay Description:Inhibitory activity of the compound against Serine protease chymotrypsinMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed