Affinity DataKi: 0.00100nMAssay Description:Inhibition of HIV1 protease using RE(Edans)SGIFLETSK(Dabcyl)R as substrate by fluorescence methodMore data for this Ligand-Target Pair
Affinity DataKi: 0.00800nMAssay Description:Binding affinity to wild type HIV1 proteaseMore data for this Ligand-Target Pair
Affinity DataKi: 0.0100nMAssay Description:Inhibition of HIV1 protease using RE(Edans)SGIFLETSK(Dabcyl)R as substrate by fluorescence methodMore data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Southern Research Institute
Curated by ChEMBL
Southern Research Institute
Curated by ChEMBL
Affinity DataKi: 0.340nMAssay Description:Inhibition of human recombinant cyclophilin-associted cis-trans propyl isomerase activityMore data for this Ligand-Target Pair
Affinity DataKi: 1.70nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
Affinity DataKi: 1.70nMAssay Description:Inhibition of HIV1 protease using Pr SF-2-WTQ7K-Pr as substrate after 24 hrs by LC/MS-MS analysisMore data for this Ligand-Target Pair
Affinity DataKi: 1.70nMAssay Description:Inhibition of HIV1 protease after 48 hrs by micro-titer plate assayMore data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Southern Research Institute
Curated by ChEMBL
Southern Research Institute
Curated by ChEMBL
Affinity DataKi: 2.11nMAssay Description:Inhibition of human recombinant cyclophilin-associted cis-trans propyl isomerase activityMore data for this Ligand-Target Pair
Affinity DataKi: 3nMAssay Description:Binding affinity of the compound was tested against L929 cells AdoHcy hydrolase activityMore data for this Ligand-Target Pair
Affinity DataKi: 4nMAssay Description:Inhibition of HIV1 protease after 48 hrs by micro-titer plate assayMore data for this Ligand-Target Pair
Affinity DataKi: 4nMAssay Description:Inhibition of HIV1 proteaseMore data for this Ligand-Target Pair
Affinity DataKi: 8nMAssay Description:Inhibition of HIV1 protease after 48 hrs by micro-titer plate assayMore data for this Ligand-Target Pair
TargetSodium- and chloride-dependent GABA transporter 1(Rattus norvegicus)
Shandong University
Curated by ChEMBL
Shandong University
Curated by ChEMBL
Affinity DataKi: 8.10nMAssay Description:Inhibition of NO711 binding to mouse GAT1 receptor expressed in HEK293 cell membranes incubated for 1 hr by LC-ESI-MS/MS analysisMore data for this Ligand-Target Pair
Affinity DataKi: 9.70nMAssay Description:Inhibition of HIV1 protease G48V mutantMore data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Homo sapiens (Human))
Southern Research Institute
Curated by ChEMBL
Southern Research Institute
Curated by ChEMBL
Affinity DataKi: 9.79nMAssay Description:Inhibition of human recombinant cyclophilin-associted cis-trans propyl isomerase activityMore data for this Ligand-Target Pair
Affinity DataKi: 10nMAssay Description:Inhibition of HIV1 protease V82F mutantMore data for this Ligand-Target Pair
Affinity DataKi: 11.1nMAssay Description:Binding affinity of the compound was tested against L929 cells AdoHcy hydrolase activityMore data for this Ligand-Target Pair
Affinity DataKi: 13nMAssay Description:Inhibition of HIV1 protease V82F mutantMore data for this Ligand-Target Pair
Affinity DataKi: 16nMAssay Description:Binding affinity to wild type HIV1 proteaseMore data for this Ligand-Target Pair
Affinity DataKi: 22nMAssay Description:Inhibition of HIV1 protease G48V mutantMore data for this Ligand-Target Pair
Affinity DataKi: 27nMAssay Description:Inhibition of HIV1 protease V82A mutantMore data for this Ligand-Target Pair
Affinity DataKi: 30nMAssay Description:Inhibition of HIV1 protease V82A mutantMore 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: 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: 86nMAssay Description:Inhibitory effect of the compound against L929 Cell S-adenosyl-L-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
TargetSodium- and chloride-dependent GABA transporter 1(Rattus norvegicus)
Shandong University
Curated by ChEMBL
Shandong University
Curated by ChEMBL
Affinity DataKi: 117nMAssay Description:Inhibition of NO711 binding to mouse GAT1 receptor expressed in HEK293 cell membranes incubated for 1 hr by LC-ESI-MS/MS analysisMore 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: 150nMAssay Description:Inhibitory effect of the compound against L929 Cell 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: 310nMAssay Description:Inhibitory effect on Lactobacillus casei thymidylate synthaseMore data for this Ligand-Target Pair
Affinity DataKi: 550nMAssay Description:Inhibition of recombinant Placental AdenosylhomocysteinaseMore data for this Ligand-Target Pair
Affinity DataKi: 590nMAssay Description:Ability to inhibit the thymidylate synthase from L. casei was determined and expressed as inhibition constant(Ki)More data for this Ligand-Target Pair
Affinity DataKi: 610nMAssay Description:Inhibitory effect on Lactobacillus casei thymidylate synthaseMore data for this Ligand-Target Pair
Affinity DataKi: 610nMAssay Description:Ability to inhibit the thymidylate synthase from L. casei was determined and expressed as inhibition constant(Ki)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: 681nMAssay 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: 960nMAssay Description:Inhibitory effect on Lactobacillus casei thymidylate synthaseMore 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: 1.13E+3nMAssay Description:Inhibitory effect on Lactobacillus casei thymidylate synthaseMore data for this Ligand-Target Pair
Affinity DataKi: 1.21E+3nMAssay Description:Inhibitory effect on Lactobacillus casei thymidylate synthaseMore data for this Ligand-Target Pair
Affinity DataKi: 1.30E+3nMAssay Description:Ability to inhibit the thymidylate synthase from L. casei was determined and expressed as inhibition constant(Ki)More 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
Affinity DataKi: 1.40E+3nMAssay Description:Ability to inhibit the thymidylate synthase from L. casei was determined and expressed as inhibition constant(Ki)More data for this Ligand-Target Pair
Affinity DataKi: 1.41E+3nMAssay Description:Inhibitory effect on Lactobacillus casei thymidylate synthaseMore 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