Compile Data Set for Download or QSAR
Report error Found 10 Enz. Inhib. hit(s) with all data for entry = 50015205
TargetCathepsin S(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50152984BDBM50152984(1-(4-Phenyl-piperazin-1-yl)-3-(3-phenyl-4,5,6,7-te...)
Affinity DataIC50: 5nMAssay Description:Inhibitory concentration against human cysteine protease cathepsin SMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin S(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50152989BDBM50152989(Carbamic acid 2-[5-carbamoyl-3-(4-iodo-phenyl)-4,5...)
Affinity DataIC50: 20nMAssay Description:Inhibitory concentration against human cysteine protease cathepsin SMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin S(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50152985BDBM50152985(1-{3-[4-(2-Cyano-phenyl)-piperazin-1-yl]-2-hydroxy...)
Affinity DataIC50: 50nMAssay Description:Inhibitory concentration against human cysteine protease cathepsin SMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin S(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50152988BDBM50152988(2-(4-{3-[5-Acetyl-3-(4-iodo-phenyl)-4,5,6,7-tetrah...)
Affinity DataIC50: 120nMAssay Description:Inhibitory concentration against human cysteine protease cathepsin SMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin S(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50152990BDBM50152990(1-[1-{2-Hydroxy-3-[4-(2-methoxy-phenyl)-piperazin-...)
Affinity DataIC50: 600nMAssay Description:Inhibitory concentration against human cysteine protease cathepsin SMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin S(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50152986BDBM50152986(1-(3-(4-Chloro-phenyl)-1-{3-[4-(2-chloro-phenyl)-p...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory concentration against human cysteine protease cathepsin SMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin S(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50152992BDBM50152992(1-[1-(3-{4-[Bis-(4-fluoro-phenyl)-methyl]-piperazi...)
Affinity DataIC50: 1.00E+3nMAssay Description:Inhibitory concentration against human cysteine protease cathepsin SMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin S(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50152991BDBM50152991(1-(3-(4-Chloro-phenyl)-1-{2-hydroxy-3-[4-(2-methox...)
Affinity DataIC50: 2.10E+3nMAssay Description:Inhibitory concentration against human cysteine protease cathepsin SMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin S(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50152987BDBM50152987(1-(3-(4-Chloro-phenyl)-1-{4-[4-(2-methoxy-phenyl)-...)
Affinity DataIC50: 9.50E+3nMAssay Description:Inhibitory concentration against human cysteine protease cathepsin SMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed
TargetCathepsin S(Human)
Johnson & Johnson Pharmaceutical Research and Development

Curated by ChEMBL
LigandChemical structure of BindingDB Monomer ID 50152983BDBM50152983(1-[2-Hydroxy-3-(4-o-tolyl-piperazin-1-yl)-propyl]-...)
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibitory concentration against human cysteine protease cathepsin SMore data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed