Report error Found 97 with Last Name = 'may' and Initial = 'wj'
Affinity DataKi: 8.00E+4nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 1.70E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 2.50E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 2.50E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 3.10E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 3.50E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 3.80E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 3.80E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 3.80E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 4.00E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 4.20E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 4.25E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 4.30E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 4.50E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 4.50E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 4.70E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 4.80E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 5.00E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 5.90E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 6.40E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataKi: 8.00E+5nMAssay Description:In vitro apparent inhibition constant of porcine renal Dehydropeptidase-1.More data for this Ligand-Target Pair
Affinity DataIC50: 300nMpH: 7.0 T: 37°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using metallo-beta-lactamase.More data for this Ligand-Target Pair
Affinity DataIC50: 400nMpH: 7.0 T: 37°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using metallo-beta-lactamase.More data for this Ligand-Target Pair
Affinity DataIC50: 1.80E+3nMpH: 7.0 T: 37°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using metallo-beta-lactamase.More data for this Ligand-Target Pair
Affinity DataIC50: 1.90E+3nMpH: 7.0 T: 37°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using metallo-beta-lactamase.More data for this Ligand-Target Pair
Affinity DataIC50: 3.50E+3nMpH: 7.0 T: 37°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using metallo-beta-lactamase.More data for this Ligand-Target Pair
Affinity DataIC50: 4.00E+3nMpH: 7.0 T: 37°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using metallo-beta-lactamase.More data for this Ligand-Target Pair
Affinity DataIC50: 6.00E+3nMpH: 7.0 T: 37°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using metallo-beta-lactamase.More data for this Ligand-Target Pair
Affinity DataIC50: 7.00E+3nMpH: 7.0 T: 37°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using metallo-beta-lactamase.More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Bacteroides fragilis)
Merck Research Laboratories
Curated by ChEMBL
Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.80E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Bacteroides fragilis.More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Bacteroides fragilis)
Merck Research Laboratories
Curated by ChEMBL
Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 2.20E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Bacteroides fragilis.More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Bacteroides fragilis)
Merck Research Laboratories
Curated by ChEMBL
Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 3.00E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Bacteroides fragilis.More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Bacteroides fragilis)
Merck Research Laboratories
Curated by ChEMBL
Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 3.30E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Bacteroides fragilis.More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Bacteroides fragilis)
Merck Research Laboratories
Curated by ChEMBL
Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 3.70E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Bacteroides fragilis.More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Bacteroides fragilis)
Merck Research Laboratories
Curated by ChEMBL
Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 4.00E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Bacteroides fragilis.More data for this Ligand-Target Pair
Affinity DataIC50: 4.20E+4nMpH: 7.0 T: 37°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using metallo-beta-lactamase.More data for this Ligand-Target Pair
Affinity DataIC50: 4.20E+4nMpH: 7.0 T: 37°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using metallo-beta-lactamase.More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Bacteroides fragilis)
Merck Research Laboratories
Curated by ChEMBL
Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Bacteroides fragilis.More data for this Ligand-Target Pair
Affinity DataIC50: 6.00E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Pseudomonas aeruginosa mediated by the plasmid-borne IMP-1 enzyme.More data for this Ligand-Target Pair
Affinity DataIC50: 6.50E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Pseudomonas aeruginosa mediated by the plasmid-borne IMP-1 enzyme.More data for this Ligand-Target Pair
Affinity DataIC50: 6.60E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Pseudomonas aeruginosa mediated by the plasmid-borne IMP-1 enzyme.More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Bacteroides fragilis)
Merck Research Laboratories
Curated by ChEMBL
Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 7.00E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Bacteroides fragilis.More data for this Ligand-Target Pair
Affinity DataIC50: 7.00E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Pseudomonas aeruginosa mediated by the plasmid-borne IMP-1 enzyme.More data for this Ligand-Target Pair
Affinity DataIC50: 7.60E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Pseudomonas aeruginosa mediated by the plasmid-borne IMP-1 enzyme.More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Bacteroides fragilis)
Merck Research Laboratories
Curated by ChEMBL
Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 8.00E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Bacteroides fragilis.More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Bacteroides fragilis)
Merck Research Laboratories
Curated by ChEMBL
Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 8.00E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Bacteroides fragilis.More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Bacteroides fragilis)
Merck Research Laboratories
Curated by ChEMBL
Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 8.00E+4nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Bacteroides fragilis.More data for this Ligand-Target Pair
TargetMetallo-beta-lactamase type 2(Bacteroides fragilis)
Merck Research Laboratories
Curated by ChEMBL
Merck Research Laboratories
Curated by ChEMBL
Affinity DataIC50: 1.00E+5nMAssay Description:Inhibition of metallo-beta-lactamase (MBL) from Bacteroides fragilis.More data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMpH: 7.0 T: 37°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+5nMpH: 7.0 T: 37°CAssay Description:Enzyme inhibition assay by biphenyl tetrazoles (BPTS)using dehydropeptidase 1 (DPH-1).More data for this Ligand-Target Pair