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Found 9 with Last Name = 'biernacki' and Initial = 'k'
TargetSteryl-sulfatase(Homo sapiens (Human))
Gdask University Of Technology

Curated by ChEMBL
LigandPNGBDBM50134329(CHEMBL122708 | Sulfamic acid (11R,12S,15S,16S)-13-...)
Affinity DataIC50:  0.0650nMAssay Description:Inhibition of STS in human MCF7 cells assessed as reduction in [3H]estradiol and [3H]estrone formation using [3H]estrone sulfate as substrate incubat...More data for this Ligand-Target Pair
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TargetSteryl-sulfatase(Homo sapiens (Human))
Gdask University Of Technology

Curated by ChEMBL
LigandPNGBDBM50604012(CHEMBL5199004)
Affinity DataIC50:  0.210nMAssay Description:Inhibition of STS in human MCF7 cells using [3H]E1S as substrate incubated for 20 hrs by radioisotope cellular assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
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TargetSteryl-sulfatase(Homo sapiens (Human))
Gdask University Of Technology

Curated by ChEMBL
LigandPNGBDBM13058(6-oxo-6,7,8,9,10,11-hexahydrocyclohepta[c]chromen-...)
Affinity DataIC50:  1.10nMAssay Description:Inhibition of STS in human MCF7 cells using [3H]E1S as substrate incubated for 20 hrs by radioisotope cellular assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Gdask University Of Technology

Curated by ChEMBL
LigandPNGBDBM50604009(CHEMBL5170413)
Affinity DataIC50:  1.70nMAssay Description:Inhibition of STS in human MCF7 cells using [3H]E1S as substrate incubated for 20 hrs by radioisotope cellular assayMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Gdask University Of Technology

Curated by ChEMBL
LigandPNGBDBM50604011(CHEMBL5205557)
Affinity DataIC50:  1.70nMAssay Description:Inhibition of STS in human MCF7 cells using [3H]E1S as substrate incubated for 20 hrs by radioisotope cellular assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Gdask University Of Technology

Curated by ChEMBL
LigandPNGBDBM50604008(CHEMBL5179747)
Affinity DataIC50:  1.90nMAssay Description:Inhibition of STS in human MCF7 cells using [3H]E1S as substrate incubated for 20 hrs by radioisotope cellular assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Gdask University Of Technology

Curated by ChEMBL
LigandPNGBDBM50604010(CHEMBL5169672)
Affinity DataIC50:  3nMAssay Description:Inhibition of STS in human MCF7 cells using [3H]E1S as substrate incubated for 20 hrs by radioisotope cellular assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Gdask University Of Technology

Curated by ChEMBL
LigandPNGBDBM50604012(CHEMBL5199004)
Affinity DataIC50:  37nMAssay Description:Inhibition of human placental STS using [3H]E1S as substrate incubated for 3 hrs by radioisotope enzymatic assayMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails PubMed
TargetSteryl-sulfatase(Homo sapiens (Human))
Gdask University Of Technology

Curated by ChEMBL
LigandPNGBDBM50051829(4-methyl-2-oxo-2H-chromen-7-yl sulfamate | CHEMBL1...)
Affinity DataIC50:  380nMAssay Description:Inhibition of STS in human MCF7 cells assessed as reduction in [3H]estradiol and [3H]estrone formation using [3H]estrone sulfate as substrate incubat...More data for this Ligand-Target Pair
In DepthDetails PubMed