TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 12nMAssay Description:Inhibitory constant against human Steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 76nMAssay Description:Inhibitory activity against Steroid sulfatase expressed in CHO cellsMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 76nMAssay Description:Inhibitory constant against human steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 190nMAssay Description:Inhibitory activity against human steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 210nMAssay Description:Inhibitory activity against human steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 220nMAssay Description:Inhibitory constant against human steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 470nMAssay Description:Inhibitory constant against human steroid sulfatase in CHO cellsMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 500nMAssay Description:Inhibitory activity against human steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 530nMAssay Description:Inhibitory activity against human steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 530nMAssay Description:Inhibitory constant against purified human Steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 670nMAssay Description:Inhibitory activity against human steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 670nMAssay Description:Inhibitory constant against human steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 670nMAssay Description:Inhibitory activity against purified human Steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 890nMAssay Description:Inhibitory activity against Steroid sulfatase expressed in CHO cellsMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 1.85E+3nMAssay Description:Inhibitory activity against Steroid sulfatase expressed in CHO cellsMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 2.20E+3nMAssay Description:Inhibitory activity against human steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 2.40E+3nMAssay Description:Inhibitory activity against Steroid sulfatase expressed in CHO cellsMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 2.40E+3nMAssay Description:Inhibitory constant against human steroid sulfataseMore data for this Ligand-Target Pair
TargetHistone deacetylase 7(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: 2.50E+3nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 3.20E+3nMAssay Description:Inhibitory activity against human steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 5.80E+3nMAssay Description:Inhibitory constant against purified human Steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 6.00E+3nMAssay Description:Inhibitory constant against human steroid sulfatase in CHO cellsMore data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: 7.00E+3nMAssay Description:Inhibition of human HDAC1 using Boc-Lys(Ac)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 mins by trypsi...More data for this Ligand-Target Pair
TargetHistone deacetylase 8(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: 8.40E+3nMAssay Description:Binding affinity at 5-hydroxytryptamine 4 receptor in rat striatum by [3H]GR-113808 displacement.More data for this Ligand-Target Pair
TargetHistone deacetylase 5(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: 1.20E+4nMAssay Description:Inhibition of human HDAC5 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
TargetHistone deacetylase 5(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: 1.30E+4nMAssay Description:Inhibition of human HDAC5 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: 1.40E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 1.45E+4nMAssay Description:Inhibitory constant against human steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 1.61E+4nMAssay Description:Inhibitory constant against human steroid sulfataseMore data for this Ligand-Target Pair
TargetHistone deacetylase 6(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: 2.00E+4nMAssay Description:Inhibitory potency against Varicella zoster virus ribonucleotide reductaseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: >2.00E+4nMAssay Description:Inhibitory activity against human steroid sulfataseMore data for this Ligand-Target Pair
TargetSteryl-sulfatase(Homo sapiens (Human))
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Novartis Institutes For Biomedical Research
Curated by ChEMBL
Affinity DataKi: 3.20E+4nMAssay Description:Inhibitory activity against human steroid sulfataseMore data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC1 using Boc-Lys(Ac)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 mins by trypsi...More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC1 using Boc-Lys(Ac)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 mins by trypsi...More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Inhibition of human HDAC4 using Boc-Lys(trifluoroacetyl)-AMC as substrate preincubated for 30 mins followed by substrate addition measured after 60 m...More data for this Ligand-Target Pair
TargetHistone deacetylase 5(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:In vitro relaxation of carbachol pre-contracted rat oesophageal TMM.More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
TargetHistone deacetylase 8(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
TargetHistone deacetylase 1(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
TargetHistone deacetylase 4(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair
TargetHistone deacetylase 5(Homo sapiens (Human))
University Of Applied Sciences Darmstadt
Curated by ChEMBL
University Of Applied Sciences Darmstadt
Curated by ChEMBL
Affinity DataKi: >5.00E+4nMAssay Description:Binding affinity at 5-hydroxytryptamine 3 receptor in rat entorhinal cortex by [3H]BRL-43694 displacement.More data for this Ligand-Target Pair