Compile Data Set for Download or QSAR
maximum 50k data
Found 11 Enz. Inhib. hit(s) with all data for entry = 50016503
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50148291(((S)-1-Formyl-pentyl)-carbamic acid (S)-2-cyclohex...)
Affinity DataIC50:  2.70nMAssay Description:Inhibition of 10 uM Cbz-Phe-Arg-AMC binding to human cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50169767(2-[(S)-2-((S)-2-Cyclohexyl-1-methyl-ethoxycarbonyl...)
Affinity DataIC50:  230nMAssay Description:Inhibition of 10 uM Cbz-Phe-Arg-AMC binding to human cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50169766(CHEMBL183796 | [(S)-1-(Thiophene-2-carbonyl)-penty...)
Affinity DataIC50:  1.90E+3nMAssay Description:Inhibition of 10 uM Cbz-Phe-Arg-AMC binding to human cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50169769((S)-1-cyclohexylpropan-2-yl (S)-1-oxo-1-(thiazol-2...)
Affinity DataIC50:  3.10E+3nMAssay Description:Inhibition of 10 uM Cbz-Phe-Arg-AMC binding to human cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50169770((S)-1-cyclohexylpropan-2-yl (S)-1-oxo-1-(5-phenyl-...)
Affinity DataIC50:  4.00E+3nMAssay Description:Inhibition of 10 uM Cbz-Phe-Arg-AMC binding to human cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50169762((S)-1-cyclohexylpropan-2-yl (S)-1-oxo-1-(4-phenylt...)
Affinity DataIC50:  7.10E+3nMAssay Description:Inhibition of 10 uM Cbz-Phe-Arg-AMC binding to human cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50169765((S)-1-cyclohexylpropan-2-yl (S)-1-(5-methyl-1,2,4-...)
Affinity DataIC50:  8.10E+3nMAssay Description:Inhibition of 10 uM Cbz-Phe-Arg-AMC binding to human cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50169764(CHEMBL182539 | [(S)-1-(4-Trifluoromethyl-thiazole-...)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibition of 10 uM Cbz-Phe-Arg-AMC binding to human cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50169768(2-[(S)-2-((S)-2-Benzyloxycarbonylamino-4-methyl-pe...)
Affinity DataIC50:  1.30E+4nMAssay Description:Inhibition of 10 uM Cbz-Phe-Arg-AMC binding to human cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50169771(2-[(S)-2-(1-Benzyl-propoxycarbonylamino)-hexanoyl]...)
Affinity DataIC50: >1.30E+4nMAssay Description:Inhibition of 10 uM Cbz-Phe-Arg-AMC binding to human cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50169763(2-[2-(2-Propoxy-benzoylamino)-acetyl]-thiazole-4-c...)
Affinity DataIC50: >1.30E+4nMAssay Description:Inhibition of 10 uM Cbz-Phe-Arg-AMC binding to human cathepsin K by fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed