Compile Data Set for Download or QSAR
maximum 50k data
Found 32 Enz. Inhib. hit(s) with all data for entry = 50031447
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313524(3,5-dioxo-4-(3-(piperidin-1-yl)propyl)-2-(3-(trifl...)
Affinity DataIC50:  17nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313514(2-cycloheptyl-3,5-dioxo-4-propyl-2,3,4,5-tetrahydr...)
Affinity DataIC50:  38nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313531(2-(3-isopropylphenyl)-3,5-dioxo-4-(3-(piperidin-1-...)
Affinity DataIC50:  38nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313507(2-(3-isopropylphenyl)-3,5-dioxo-4-propyl-2,3,4,5-t...)
Affinity DataIC50:  72nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313529(2-cycloheptyl-3,5-dioxo-4-(3-(piperidin-1-yl)propy...)
Affinity DataIC50:  100nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313523(4-(3-(dimethylamino)propyl)-3,5-dioxo-2-(3-(triflu...)
Affinity DataIC50:  100nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313528(2-cycloheptyl-4-(3-(dimethylamino)propyl)-3,5-diox...)
Affinity DataIC50:  110nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313527(4-(3-morpholinopropyl)-3,5-dioxo-2-(3-(trifluorome...)
Affinity DataIC50:  112nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313525(3,5-dioxo-4-(2-(piperidin-1-yl)ethyl)-2-(3-(triflu...)
Affinity DataIC50:  182nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313513(2-cyclohexyl-3,5-dioxo-4-propyl-2,3,4,5-tetrahydro...)
Affinity DataIC50:  197nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313508(2-(3-tert-butylphenyl)-3,5-dioxo-4-propyl-2,3,4,5-...)
Affinity DataIC50:  288nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313530(2-cycloheptyl-4-(3-morpholinopropyl)-3,5-dioxo-2,3...)
Affinity DataIC50:  500nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313526(4-(2-(dimethylamino)ethyl)-3,5-dioxo-2-(3-(trifluo...)
Affinity DataIC50:  810nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313512(2-cyclopentyl-3,5-dioxo-4-propyl-2,3,4,5-tetrahydr...)
Affinity DataIC50:  870nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313521(4-benzyl-3,5-dioxo-2-(3-(trifluoromethyl)phenyl)-2...)
Affinity DataIC50:  1.00E+3nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313515(2-(cyclohexylmethyl)-3,5-dioxo-4-propyl-2,3,4,5-te...)
Affinity DataIC50:  1.10E+3nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313519(4-cyclopentyl-3,5-dioxo-2-(3-(trifluoromethyl)phen...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313503(3,5-dioxo-4-propyl-2-(3-(trifluoromethyl)phenyl)-2...)
Affinity DataIC50:  2.00E+3nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313517(4-ethyl-3,5-dioxo-2-(3-(trifluoromethyl)phenyl)-2,...)
Affinity DataIC50:  2.50E+3nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313506(3,5-dioxo-4-propyl-2-m-tolyl-2,3,4,5-tetrahydro-1,...)
Affinity DataIC50:  3.50E+3nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313522(3,5-dioxo-4-phenethyl-2-(3-(trifluoromethyl)phenyl...)
Affinity DataIC50:  4.46E+3nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313518(4-methyl-3,5-dioxo-2-(3-(trifluoromethyl)phenyl)-2...)
Affinity DataIC50:  4.78E+3nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313516(4-butyl-3,5-dioxo-2-(3-(trifluoromethyl)phenyl)-2,...)
Affinity DataIC50:  7.40E+3nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313511(2-(3-(hydroxymethyl)phenyl)-3,5-dioxo-4-propyl-2,3...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313510(2-(3-methoxyphenyl)-3,5-dioxo-4-propyl-2,3,4,5-tet...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313509(2-(biphenyl-3-yl)-3,5-dioxo-4-propyl-2,3,4,5-tetra...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313505(3,5-dioxo-2-phenyl-4-propyl-2,3,4,5-tetrahydro-1,2...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313524(3,5-dioxo-4-(3-(piperidin-1-yl)propyl)-2-(3-(trifl...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of cathepsin SMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313504(3,5-dioxo-4-propyl-2-(4-(trifluoromethyl)phenyl)-2...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313524(3,5-dioxo-4-(3-(piperidin-1-yl)propyl)-2-(3-(trifl...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of cathepsin BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProcathepsin L(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313524(3,5-dioxo-4-(3-(piperidin-1-yl)propyl)-2-(3-(trifl...)
Affinity DataIC50: >1.00E+4nMAssay Description:Inhibition of cathepsin LMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Schering-Plough

Curated by ChEMBL
LigandPNGBDBM50313520(3,5-dioxo-4-phenyl-2-(3-(trifluoromethyl)phenyl)-2...)
Affinity DataIC50:  1.20E+4nMAssay Description:Inhibition of human recombinant cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed