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Found 21 with Last Name = 'begley' and Initial = 'dw'
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM18795((2S)-2-[(5-{methyl[(2-methyl-4-oxo-1,4-dihydroquin...)
Affinity DataIC50:  900nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82167(MV1555)
Affinity DataIC50:  3.00E+4nM Kd:  5.00E+3nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82175(MV1570)
Affinity DataIC50:  7.00E+4nM Kd:  2.00E+3nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82174(MV1565)
Affinity DataIC50:  7.00E+4nM Kd:  1.00E+3nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82169(MV1586)
Affinity DataIC50:  1.15E+5nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82170(MV1588)
Affinity DataIC50:  1.15E+5nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82176(MV1576)
Affinity DataIC50:  1.40E+5nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82171(MV1554)
Affinity DataIC50:  1.60E+5nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82173(MV1561)
Affinity DataIC50:  1.60E+5nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82166(MV1556)
Affinity DataIC50:  2.40E+5nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82172(MV1557)
Affinity DataIC50:  2.60E+5nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82177(MV1574)
Affinity DataIC50: >5.00E+5nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82168(MV1581)
Affinity DataIC50: >5.00E+5nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetThymidylate synthase(Homo sapiens (Human))
University of Washington

LigandPNGBDBM82178(MV1578)
Affinity DataIC50: >5.00E+5nMpH: 7.5 T: 2°CAssay Description:A tritium release assay was used to determin the in vitro inhibitory strengths of various compounds. The inhibitory potency of human TS was determin...More data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails ArticlePubMed
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Burkholderia pseudomallei (strain K96243))
Northern Illinois University

Curated by ChEMBL
LigandPNGBDBM50443773(CHEMBL1230528)
Affinity DataKd:  1.35E+5nMAssay Description:Binding affinity to Burkolderia pseudomallei IspF by surface plasmon resonance methodMore data for this Ligand-Target Pair
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Burkholderia pseudomallei (strain K96243))
Northern Illinois University

Curated by ChEMBL
LigandPNGBDBM50443774(CHEMBL3094106)
Affinity DataKd:  9.00E+4nMAssay Description:Binding affinity to Burkolderia pseudomallei IspF by surface plasmon resonance methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Burkholderia pseudomallei (strain K96243))
Northern Illinois University

Curated by ChEMBL
LigandPNGBDBM50194153(5'-CDP | CDP | CHEMBL425252 | Cytidine | Cytidine ...)
Affinity DataKd:  7.50E+4nMAssay Description:Binding affinity to Burkolderia pseudomallei IspF by surface plasmon resonance methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Burkholderia pseudomallei (strain K96243))
Northern Illinois University

Curated by ChEMBL
LigandPNGBDBM50443772(CHEMBL1230597)
Affinity DataKd:  1.80E+5nMAssay Description:Binding affinity to Burkolderia pseudomallei IspF by surface plasmon resonance methodMore data for this Ligand-Target Pair
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Burkholderia pseudomallei (strain K96243))
Northern Illinois University

Curated by ChEMBL
LigandPNGBDBM50443770(CHEMBL3094104)
Affinity DataKd:  7.00E+4nMAssay Description:Binding affinity to Burkolderia pseudomallei IspF by surface plasmon resonance methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Burkholderia pseudomallei (strain K96243))
Northern Illinois University

Curated by ChEMBL
LigandPNGBDBM50443775(CHEMBL3094105)
Affinity DataKd:  2.00E+5nMAssay Description:Binding affinity to Burkolderia pseudomallei IspF by surface plasmon resonance methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target2-C-methyl-D-erythritol 2,4-cyclodiphosphate synthase(Burkholderia pseudomallei (strain K96243))
Northern Illinois University

Curated by ChEMBL
LigandPNGBDBM50443771(CHEMBL3094103)
Affinity DataKd:  1.48E+5nMAssay Description:Binding affinity to Burkolderia pseudomallei IspF by surface plasmon resonance methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed