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Found 12 Enz. Inhib. hit(s) with all data for entry = 50039213
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321626(CHEMBL1171504 | N-(2-chloro-5-(1-(3-(4-(6-chloro-3...)
Affinity DataIC50:  40nMAssay Description:Inhibition of human cathepsin SMore data for this Ligand-Target Pair
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321625(CHEMBL1171503 | CatS_4 | N-(2-chloro-5-(2-(3-(4-(6...)
Affinity DataIC50:  60nMAssay Description:Inhibition of human cathepsin SMore data for this Ligand-Target Pair
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321627(CHEMBL1171505 | CatS_6 | N-(2-chloro-5-(4-(3-(4-(6...)
Affinity DataIC50:  110nMAssay Description:Inhibition of human cathepsin SMore data for this Ligand-Target Pair
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321624(CHEMBL1171502 | N-(2-chloro-5-(1-(3-(4-(6-chloro-3...)
Affinity DataIC50:  320nMAssay Description:Inhibition of human cathepsin SMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321623(CHEMBL1171314 | N-(2-chloro-5-(1-(3-(4-(6-chloro-3...)
Affinity DataIC50:  430nMAssay Description:Inhibition of human cathepsin SMore data for this Ligand-Target Pair
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321622(CHEMBL1170609 | N-(2-chloro-5-(6-oxo-1-(3-(4-(2-ox...)
Affinity DataIC50:  1.50E+3nMAssay Description:Inhibition of human cathepsin SMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321620(CHEMBL1171313 | N-(2-chloro-5-(6-oxo-1-(3-(4-(3-(t...)
Affinity DataIC50:  1.60E+3nMAssay Description:Inhibition of human cathepsin SMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321625(CHEMBL1171503 | CatS_4 | N-(2-chloro-5-(2-(3-(4-(6...)
Affinity DataIC50:  1.80E+3nMAssay Description:Inhibition of cathepsin S-mediated invariant chain degradation in human JY B-cells assessed as accumulation of p10 fragment by Western blot analysisMore data for this Ligand-Target Pair
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321621(CHEMBL1171608 | N-(2-chloro-5-(6-oxo-1-(3-(4-(2-ox...)
Affinity DataIC50:  2.30E+3nMAssay Description:Inhibition of human cathepsin SMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321626(CHEMBL1171504 | N-(2-chloro-5-(1-(3-(4-(6-chloro-3...)
Affinity DataIC50:  6.70E+3nMAssay Description:Inhibition of cathepsin S-mediated invariant chain degradation in human JY B-cells assessed as accumulation of p10 fragment by Western blot analysisMore data for this Ligand-Target Pair
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321627(CHEMBL1171505 | CatS_6 | N-(2-chloro-5-(4-(3-(4-(6...)
Affinity DataIC50:  8.00E+3nMAssay Description:Inhibition of cathepsin S-mediated invariant chain degradation in human JY B-cells assessed as accumulation of p10 fragment by Western blot analysisMore data for this Ligand-Target Pair
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research & Development

Curated by ChEMBL
LigandPNGBDBM50321619(CHEMBL1171421 | N-(2-chloro-5-(6-oxo-1-(3-(pyrroli...)
Affinity DataIC50:  1.40E+4nMAssay Description:Inhibition of human cathepsin SMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed