Compile Data Set for Download or QSAR
Found 33 with Last Name = 'hampton' and Initial = 'se'
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50439347(CHEMBL2420337)copy SMILEScopy InChI
Affinity DataKi:  1.00E+4nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50190543(1-((2R,4S,5R)-4-hydroxy-5-((tritylamino)methyl)-te...)copy SMILEScopy InChI
Affinity DataKi:  4.60E+4nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50439346(CHEMBL2420338)copy SMILEScopy InChI
Affinity DataKi:  4.90E+4nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50439345(CHEMBL2420339)copy SMILEScopy InChI
Affinity DataKi:  6.30E+4nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50439344(CHEMBL2420340)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50439336(CHEMBL2420333)copy SMILEScopy InChI
Affinity DataKi: >1.00E+5nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50439340(CHEMBL2420344)copy SMILEScopy InChI
Affinity DataKi:  2.86E+5nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50439342(CHEMBL2420342)copy SMILEScopy InChI
Affinity DataKi:  1.00E+6nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50439341(CHEMBL2420343)copy SMILEScopy InChI
Affinity DataKi:  1.00E+6nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50439339(CHEMBL2420336)copy SMILEScopy InChI
Affinity DataKi:  1.00E+6nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50439338(CHEMBL2420335)copy SMILEScopy InChI
Affinity DataKi:  1.00E+6nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50386635(CHEMBL2048460)copy SMILEScopy InChI
Affinity DataKi:  1.00E+6nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50439337(CHEMBL2420334)copy SMILEScopy InChI
Affinity DataKi:  1.00E+6nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetDeoxyuridine 5'-triphosphate nucleotidohydrolase, mitochondrial(Homo sapiens (Human))
University of Dundee

Curated by ChEMBL
LigandPNGBDBM50439343(CHEMBL2420341)copy SMILEScopy InChI
Affinity DataKi:  1.00E+6nMAssay Description:Inhibition of recombinant human dUTPase expressed in Escherichia coli BL21 (DE3) using dUTP as substrate by spectrophotometric analysisMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NV9KPJPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500099(CHEMBL3741765)copy SMILEScopy InChI
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500092(CHEMBL3741937)copy SMILEScopy InChI
Affinity DataIC50: 3.90E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500097(CHEMBL3740962)copy SMILEScopy InChI
Affinity DataIC50: 4.20E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500105(CHEMBL3740249)copy SMILEScopy InChI
Affinity DataIC50: 4.90E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500103(CHEMBL3742211)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500098(CHEMBL3741101)copy SMILEScopy InChI
Affinity DataIC50: 5.30E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500106(CHEMBL3741673)copy SMILEScopy InChI
Affinity DataIC50: 5.40E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500094(CHEMBL3740203)copy SMILEScopy InChI
Affinity DataIC50: 6.70E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500101(CHEMBL1979298)copy SMILEScopy InChI
Affinity DataIC50: 6.90E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500091(CHEMBL3740563)copy SMILEScopy InChI
Affinity DataIC50: 7.10E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500100(CHEMBL3740034)copy SMILEScopy InChI
Affinity DataIC50: 8.20E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500095(CHEMBL2003928)copy SMILEScopy InChI
Affinity DataIC50: 8.80E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500107(CHEMBL3741464)copy SMILEScopy InChI
Affinity DataIC50: 8.90E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500102(CHEMBL3740606)copy SMILEScopy InChI
Affinity DataIC50: 9.40E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500109(CHEMBL3740547)copy SMILEScopy InChI
Affinity DataIC50: 9.80E+3nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500093(CHEMBL2006267)copy SMILEScopy InChI
Affinity DataIC50: 1.10E+4nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500096(CHEMBL3739720)copy SMILEScopy InChI
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500108(CHEMBL3740917)copy SMILEScopy InChI
Affinity DataIC50: 1.60E+4nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed
TargetCAAX prenyl protease 2(Homo sapiens (Human))
New York University Abu Dhabi

Curated by ChEMBL
LigandPNGBDBM50500104(CHEMBL3739592)copy SMILEScopy InChI
Affinity DataIC50: 3.80E+4nMAssay Description:Inhibition of human Rce1-mediated CaaX protease activity using ABZ-KSKTKC(farnesyl)QIIM and ABZ-KSKTKC(farnesyl)VIQI as substrate assessed as residua...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2NS0XXQPubMed