Compile Data Set for Download or QSAR
maximum 50k data
Found 6 of ic50 for monomerid = 50152520
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50152520(1-benzylcyclopentyl(S)-1,2-dioxo-1-((R)-1-phenylet...)
Affinity DataIC50:  25nMAssay Description:Inhibition of human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin K(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50152520(1-benzylcyclopentyl(S)-1,2-dioxo-1-((R)-1-phenylet...)
Affinity DataIC50:  25.1nMAssay Description:Inhibition of human cathepsin KMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin S(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50152520(1-benzylcyclopentyl(S)-1,2-dioxo-1-((R)-1-phenylet...)
Affinity DataIC50:  430nMAssay Description:Inhibition of 10 uM Cbz-Val-Val-Arg-AMC binding to human cathepsin S in fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProcathepsin L(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50152520(1-benzylcyclopentyl(S)-1,2-dioxo-1-((R)-1-phenylet...)
Affinity DataIC50:  3.00E+3nMAssay Description:Inhibition of 5 uM Cbz-Phe-Arg-AMC human cathepsin L in fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPro-cathepsin H(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50152520(1-benzylcyclopentyl(S)-1,2-dioxo-1-((R)-1-phenylet...)
Affinity DataIC50: >1.20E+4nMAssay Description:Inhibition of 50 uM L-Arg-beta-naphthalamide binding to human cathepsin H in fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin B(Homo sapiens (Human))
Glaxosmithkline

Curated by ChEMBL
LigandPNGBDBM50152520(1-benzylcyclopentyl(S)-1,2-dioxo-1-((R)-1-phenylet...)
Affinity DataIC50: >1.20E+4nMAssay Description:Inhibition of 10 uM Cbz-Phe-Arg-AMC binding to human cathepsin B in fluorescence assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed