Affinity DataKi: 39nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
Affinity DataKi: 39nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
Affinity DataKi: 39nMAssay Description:Inhibitory activity against recombinant rat liver S-adenosyl-homocysteine hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 39nMAssay Description:Inhibitory activity against recombinant rat liver S-adenosyl-homocysteine hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 40nMAssay Description:Inhibitory activity against recombinant rat liver S-adenosyl-homocysteine hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 43nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
Affinity DataKi: 43nMAssay Description:Inhibitory activity against recombinant rat liver S-adenosyl-homocysteine hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 95nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
Affinity DataKi: 96nMAssay Description:Tested for kinetic constant for the inhibition of recombinant human placental S-Adenosyl-L-homocysteine HydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 101nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
Affinity DataKi: 110nMAssay Description:Tested for kinetic constant for the inhibition of recombinant human placental S-Adenosyl-L-homocysteine HydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 111nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
Affinity DataKi: 134nMAssay Description:Tested for kinetic constant for the inhibition of recombinant human placental S-Adenosyl-L-homocysteine HydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 224nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
Affinity DataKi: 320nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
Affinity DataKi: 360nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
Affinity DataKi: 410nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University
Curated by ChEMBL
Florida International University
Curated by ChEMBL
Affinity DataKi: 430nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair
Affinity DataKi: 550nMAssay Description:Inhibition of recombinant Placental AdenosylhomocysteinaseMore data for this Ligand-Target Pair
Affinity DataKi: 570nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
Affinity DataKi: 570nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
Affinity DataKi: 670nMAssay Description:concentration dependent inhibition of S-Adenosyl-homocysteine hydrolase was determined by Kitz and Wilson methodMore data for this Ligand-Target Pair
Affinity DataKi: 670nMAssay Description:Inhibitory potency against recombinant human placental S-Adenosyl-L-homocysteine HydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 681nMAssay Description:Tested for kinetic constant for the inhibition of recombinant human placental S-Adenosyl-L-homocysteine HydrolaseMore data for this Ligand-Target Pair
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University
Curated by ChEMBL
Florida International University
Curated by ChEMBL
Affinity DataKi: 700nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair
Affinity DataKi: 710nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
Affinity DataKi: 770nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
Affinity DataKi: 1.10E+3nMAssay Description:Kinetic constant calculated from the pseudo-first-order rate constant(k app) for S-adenosyl-homocysteine hydrolase inactivationMore data for this Ligand-Target Pair
Affinity DataKi: 1.30E+3nMAssay Description:Tested for kinetic constant for the inhibition of recombinant human placental S-Adenosyl-L-homocysteine HydrolaseMore data for this Ligand-Target Pair
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University
Curated by ChEMBL
Florida International University
Curated by ChEMBL
Affinity DataKi: 1.40E+3nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair
Affinity DataKi: 1.70E+3nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
Affinity DataKi: 1.70E+3nMAssay Description:Kinetic constant calculated from the pseudo-first-order rate constant(k app) for S-adenosyl-homocysteine hydrolase inactivationMore data for this Ligand-Target Pair
Affinity DataKi: 1.93E+3nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
Affinity DataKi: 2.60E+3nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University
Curated by ChEMBL
Florida International University
Curated by ChEMBL
Affinity DataKi: 2.80E+3nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair
Affinity DataKi: 3.10E+3nMAssay Description:The kinetic constant for inhibition of S-adenosyl-homocysteine hydrolase by the compoundMore data for this Ligand-Target Pair
Affinity DataKi: 3.60E+3nMAssay Description:The kinetic constant for inhibition of S-adenosyl-homocysteine hydrolase by the compoundMore data for this Ligand-Target Pair
Affinity DataKi: 3.80E+3nMAssay Description:Kinetic constant calculated from the pseudo-first-order rate constant(k app) for S-adenosyl-homocysteine hydrolase inactivationMore data for this Ligand-Target Pair
Affinity DataKi: 3.90E+3nMAssay Description:The kinetic constant for inhibition of S-adenosyl-homocysteine hydrolase by the compoundMore data for this Ligand-Target Pair
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University
Curated by ChEMBL
Florida International University
Curated by ChEMBL
Affinity DataKi: 4.20E+3nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University
Curated by ChEMBL
Florida International University
Curated by ChEMBL
Affinity DataKi: 7.70E+3nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University
Curated by ChEMBL
Florida International University
Curated by ChEMBL
Affinity DataKi: 7.90E+3nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University
Curated by ChEMBL
Florida International University
Curated by ChEMBL
Affinity DataKi: 8.80E+3nMAssay Description:Inhibition of Bacillus subtilis LuxS assessed as enzyme-inhibitor dissociation constantMore data for this Ligand-Target Pair
Affinity DataKi: 1.00E+4nMAssay Description:Inhibitory constant for S-adenosyl-homocysteine hydrolase, was determined using Kitz and Wilson equation {Kobs = Kinact . [I]/(Ki + [I])}.More data for this Ligand-Target Pair
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University
Curated by ChEMBL
Florida International University
Curated by ChEMBL
Affinity DataKi: 1.06E+4nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair
Affinity DataKi: 1.37E+4nMAssay Description:Inhibitory constant for S-adenosyl-homocysteine hydrolase, was determined using Kitz and Wilson equation {Kobs = Kinact . [I]/(Ki + [I])}.More data for this Ligand-Target Pair
Affinity DataKi: 1.98E+4nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University
Curated by ChEMBL
Florida International University
Curated by ChEMBL
Affinity DataKi: 4.20E+4nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair
TargetS-ribosylhomocysteine lyase(Bacillus subtilis)
Florida International University
Curated by ChEMBL
Florida International University
Curated by ChEMBL
Affinity DataKi: 4.20E+4nMAssay Description:Inhibition of Bacillus subtilis LuxSMore data for this Ligand-Target Pair
Affinity DataKi: 4.34E+4nMAssay Description:Inhibition of S-adenosyl-L-homocysteine hydrolase, inactivation rate constant.More data for this Ligand-Target Pair