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Found 10 with Last Name = 'almond' and Initial = 'hj'
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50152984(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 DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50152989(3-(5-carbamoyl-3-(4-iodophenyl)-4,5,6,7-tetrahydro...)
Affinity DataIC50:  20nMAssay Description:Inhibitory concentration against human cysteine protease cathepsin SMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50152985(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 DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50152988(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 DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50152990(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 DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50152986(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 DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50152992(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 DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50152991(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 DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50152987(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 DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Johnson & Johnson Pharmaceutical Research And Development

Curated by ChEMBL
LigandPNGBDBM50152983(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 DepthDetails ArticlePubMed