Compile Data Set for Download or QSAR
maximum 50k data
Found 12 of ki data for polymerid = 50000682
TargetCathepsin F(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50392215(CHEMBL2153161)
Affinity DataKi:  21nMAssay Description:Inhibition of human recombinant cathepsin F using Z-Phe-Arg-AMC as substrate by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin F(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50392206(CHEMBL2153169)
Affinity DataKi:  3.20E+3nMAssay Description:Inhibition of human recombinant cathepsin F using Z-Phe-Arg-AMC as substrate after 8 min by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin F(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50392213(CHEMBL2153166)
Affinity DataKi: >4.00E+3nMAssay Description:Inhibition of human recombinant cathepsin F using Z-Phe-Arg-AMC as substrate after 8 min by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin F(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50392212(CHEMBL2153165)
Affinity DataKi: >4.00E+3nMAssay Description:Inhibition of human recombinant cathepsin F using Z-Phe-Arg-AMC as substrate after 8 min by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin F(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50392211(CHEMBL2153164)
Affinity DataKi: >4.00E+3nMAssay Description:Inhibition of human recombinant cathepsin F using Z-Phe-Arg-AMC as substrate after 8 min by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin F(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50392214(CHEMBL2153167)
Affinity DataKi: >4.00E+3nMAssay Description:Inhibition of human recombinant cathepsin F using Z-Phe-Arg-AMC as substrate after 8 min by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin F(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50392208(CHEMBL2153171)
Affinity DataKi: >4.00E+3nMAssay Description:Inhibition of human recombinant cathepsin F using Z-Phe-Arg-AMC as substrate after 8 min by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin F(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50392207(CHEMBL2153170)
Affinity DataKi: >4.00E+3nMAssay Description:Inhibition of human recombinant cathepsin F using Z-Phe-Arg-AMC as substrate after 8 min by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin F(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50392205(CHEMBL2153168)
Affinity DataKi: >4.00E+3nMAssay Description:Inhibition of human recombinant cathepsin F using Z-Phe-Arg-AMC as substrate after 8 min by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin F(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50392209(CHEMBL2153172)
Affinity DataKi: >4.00E+4nMAssay Description:Inhibition of human recombinant cathepsin F using Z-Phe-Arg-AMC as substrate after 8 min by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin F(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50392209(CHEMBL2153172)
Affinity DataKi: >4.00E+4nMAssay Description:Inhibition of human recombinant cathepsin F using Z-Phe-Arg-AMC as substrate after 8 min by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCathepsin F(Homo sapiens (Human))
University Of Bonn

Curated by ChEMBL
LigandPNGBDBM50392210(CHEMBL2153163)
Affinity DataKi: >4.00E+4nMAssay Description:Inhibition of human recombinant cathepsin F using Z-Phe-Arg-AMC as substrate after 8 min by fluorimetric analysisMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed