Compile Data Set for Download or QSAR
maximum 50k data
Found 6 Enz. Inhib. hit(s) with all data for entry = 50011821
TargetCathepsin D(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50084626(CHEMBL284440 | N-(2-Benzo[1,3]dioxol-5-yl-ethyl)-N...)
Affinity DataKi:  3nMAssay Description:Inhibitory activity of compound against human Cathepsin DMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin D(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50110934(CHEMBL30483 | N-((1S,3S)-1-Benzyl-3-{[2-(2,4-dichl...)
Affinity DataKi:  5.20nMAssay Description:Inhibitory activity of compound against human Cathepsin DMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin D(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50110932(CHEMBL283863 | N-(2-Benzo[1,3]dioxol-5-yl-ethyl)-3...)
Affinity DataKi:  73nMAssay Description:Inhibitory activity of compound against human Cathepsin DMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin D(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50110931(CHEMBL284441 | N-((1S,3S)-1-Benzyl-3-{[2-(2,4-dich...)
Affinity DataKi:  231nMAssay Description:Inhibitory activity of compound against human Cathepsin DMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin D(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50110933(CHEMBL30571 | N-(2-Benzo[1,3]dioxol-5-yl-ethyl)-3-...)
Affinity DataKi: >5.00E+3nMAssay Description:Inhibitory activity of compound against human Cathepsin DMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin D(Homo sapiens (Human))
University Of California

Curated by ChEMBL
LigandPNGBDBM50110935((E)-N-((1S,3S)-1-Benzyl-2-hydroxy-3-{(2-pyridin-2-...)
Affinity DataKi: >1.00E+5nMAssay Description:Inhibitory activity of compound against human Cathepsin DMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed