Compile Data Set for Download or QSAR
maximum 50k data
Found 11 Enz. Inhib. hit(s) with all data for entry = 50014632
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50145451(CHEMBL86088 | [(S)-1-((S)-2-Oxo-piperidin-3-ylamin...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibitory concentration against recombinant human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50138842(2,4-dimethylpentan-3-yl(S)-1,2-dioxo-1-((R)-1-phen...)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibitory concentration against recombinant human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50145460(CHEMBL85977 | [(S)-1-(Thiazol-4-ylmethyl)-aminooxa...)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibitory concentration against recombinant human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50145453(CHEMBL87961 | [(S)-1-(Thiazol-5-ylmethyl)-aminooxa...)
Affinity DataIC50:  1.40E+4nMAssay Description:Inhibitory concentration against recombinant human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50145457(CHEMBL421544 | [(S)-1-(Isoxazol-5-ylmethyl)-aminoo...)
Affinity DataIC50:  1.40E+4nMAssay Description:Inhibitory concentration against recombinant human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50145456(CHEMBL418935 | [(S)-1-(Thiazol-2-ylmethyl)-aminoox...)
Affinity DataIC50:  1.80E+4nMAssay Description:Inhibitory concentration against recombinant human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50145459(CHEMBL445898 | [(S)-1-([1,3,4]Oxadiazol-2-ylmethyl...)
Affinity DataIC50:  1.90E+4nMAssay Description:Inhibitory concentration against recombinant human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50145452(CHEMBL83563 | [(S)-1-(Pyridin-3-ylmethyl)-aminooxa...)
Affinity DataIC50:  2.30E+4nMAssay Description:Inhibitory concentration against recombinant human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50145454(CHEMBL87332 | [(S)-1-(Pyridin-4-ylmethyl)-aminooxa...)
Affinity DataIC50:  3.00E+4nMAssay Description:Inhibitory concentration against recombinant human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50145458(CHEMBL446669 | [(S)-1-(Pyridin-2-ylmethyl)-aminoox...)
Affinity DataIC50:  4.40E+4nMAssay Description:Inhibitory concentration against recombinant human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50145455(CHEMBL87946 | [(S)-1-((R)-1-[1,3,4]Oxadiazol-2-yl-...)
Affinity DataIC50:  5.90E+4nMAssay Description:Inhibitory concentration against recombinant human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed