Affinity DataKi: 3.80nMAssay Description:Time course of inactivation of bovine liver S-adenosyl-homocysteine hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 3.80nMAssay Description:Inhibitory activity of the compound against bovine liver S-adenosyl-L-homocysteine hydrolase (AdoHcy) rate of inactivation by NpcAMore data for this Ligand-Target Pair
Affinity DataKi: 3.80nMAssay Description:Inhibition against bovine-liver S-Adenosyl-homocysteine (AdoHcy) hydrolaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories
Curated by ChEMBL
Upjohn Laboratories
Curated by ChEMBL
Affinity DataKi: 4nMAssay Description:In vitro inhibitory activity against biotinylated human HIV-1 proteaseMore data for this Ligand-Target Pair
Affinity DataKi: 4nMAssay Description:Binding affinity against S-adenosyl-homocysteine hydrolaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories
Curated by ChEMBL
Upjohn Laboratories
Curated by ChEMBL
Affinity DataKi: 10nMAssay Description:In vitro inhibitory activity against biotinylated human HIV-1 proteaseMore data for this Ligand-Target Pair
Affinity DataKi: 12nMAssay Description:Inhibitory activity of the compound against bovine liver S-adenosyl-L-homocysteine hydrolase (AdoHcy).More data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories
Curated by ChEMBL
Upjohn Laboratories
Curated by ChEMBL
Affinity DataKi: 20nMAssay Description:In vitro inhibitory activity against biotinylated human HIV-1 proteaseMore data for this Ligand-Target Pair
Affinity DataKi: 22nMAssay Description:Inhibitory activity of the compound against bovine liver S-adenosyl-L-homocysteine hydrolase (AdoHcy).More data for this Ligand-Target Pair
Affinity DataKi: 27nMAssay Description:Inhibitory activity of the compound against bovine liver S-adenosyl-L-homocysteine hydrolase (AdoHcy).More data for this Ligand-Target Pair
Affinity DataKi: 35nMAssay Description:Time course of inactivation of bovine liver S-adenosyl-homocysteine hydrolaseMore 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:Compound was tested for its inhibitory activity against recombinant rat liver S-adenosylhomocysteine 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: 39nMAssay Description:Inhibitory activity against recombinant rat liver S-adenosyl-homocysteine hydrolaseMore data for this Ligand-Target Pair
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:Binding affinity of the compound towards purified recombinant human placental S-adenosyl-L-homocysteine hydrolaseMore data for this Ligand-Target Pair
TargetATP-dependent translocase ABCB1(Homo sapiens (Human))
The University Of Kansas
Curated by ChEMBL
The University Of Kansas
Curated by ChEMBL
Affinity DataKi: 40nMAssay Description:TP_TRANSPORTER: transepithelial transport of digoxin (basal to apical) in Caco-2 cellsMore data for this Ligand-Target Pair
Affinity DataKi: 40nMAssay Description:Compound was tested for its inhibitory activity against recombinant rat liver S-adenosylhomocysteine 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: 41nMAssay Description:Time course of inactivation of bovine 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: 43nMAssay Description:Binding affinity of the compound towards purified recombinant human placental S-adenosyl-L-homocysteine hydrolaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories
Curated by ChEMBL
Upjohn Laboratories
Curated by ChEMBL
Affinity DataKi: 45nMAssay Description:In vitro inhibitory activity against biotinylated human HIV-1 proteaseMore data for this Ligand-Target Pair
Affinity DataKi: 49nMAssay Description:Inhibitory activity of the compound against bovine liver S-adenosyl-L-homocysteine hydrolase (AdoHcy).More data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories
Curated by ChEMBL
Upjohn Laboratories
Curated by ChEMBL
Affinity DataKi: 53nMAssay Description:In vitro inhibitory activity against biotinylated human HIV-1 proteaseMore data for this Ligand-Target Pair
Affinity DataKi: 87nMAssay Description:Compound was tested for its inhibitory activity against recombinant rat liver S-adenosylhomocysteine hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 90nMAssay Description:Inhibition against bovine-liver S-Adenosyl-homocysteine (AdoHcy) 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
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories
Curated by ChEMBL
Upjohn Laboratories
Curated by ChEMBL
Affinity DataKi: >100nMAssay Description:In vitro inhibitory activity against biotinylated human HIV-1 proteaseMore 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:Binding affinity against S-adenosyl-homocysteine hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 110nMAssay Description:Inhibition against bovine-liver S-Adenosyl-homocysteine (AdoHcy) hydrolaseMore 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: 112nMAssay Description:Compound was tested for its inhibitory activity against recombinant rat liver S-adenosylhomocysteine hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 125nMAssay Description:Inhibition against bovine-liver S-Adenosyl-homocysteine (AdoHcy) hydrolaseMore data for this Ligand-Target Pair
TargetGag-Pol polyprotein [489-587](Human immunodeficiency virus type 1)
Upjohn Laboratories
Curated by ChEMBL
Upjohn Laboratories
Curated by ChEMBL
Affinity DataKi: 130nMAssay Description:In vitro inhibitory activity against biotinylated human HIV-1 proteaseMore 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: 160nMAssay Description:Inhibition against bovine-liver S-Adenosyl-homocysteine (AdoHcy) hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 166nMAssay Description:Inhibition against bovine-liver S-Adenosyl-homocysteine (AdoHcy) hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 170nMAssay Description:Inhibition against bovine-liver S-Adenosyl-homocysteine (AdoHcy) hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 180nMAssay Description:Affinity fo the compound against human Intestinal peptide transporter PepT1 in Caco-2 cells was measured as inhibition of [14C]-Gly-Sar uptakeMore data for this Ligand-Target Pair
Affinity DataKi: 200nMAssay Description:Inhibition against bovine-liver S-Adenosyl-homocysteine (AdoHcy) hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 200nMAssay Description:Inhibition against bovine-liver S-Adenosyl-homocysteine (AdoHcy) hydrolaseMore data for this Ligand-Target Pair
Affinity DataKi: 200nMAssay Description:Affinity fo the compound against human Intestinal peptide transporter PepT1 in Caco-2 cells was measured as inhibition of [14C]-Gly-Sar uptakeMore data for this Ligand-Target Pair
TargetPhenylethanolamine N-methyltransferase(Bos taurus (bovine))
University Of Kansas
Curated by ChEMBL
University Of Kansas
Curated by ChEMBL
Affinity DataKi: 210nMAssay Description:Affinity for bovine Phenylethanolamine N-MethyltransferaseMore data for this Ligand-Target Pair
TargetPhenylethanolamine N-methyltransferase(Bos taurus (bovine))
University Of Kansas
Curated by ChEMBL
University Of Kansas
Curated by ChEMBL
Affinity DataKi: 220nMAssay Description:Affinity for bovine Phenylethanolamine N-Methyltransferase (PNMT)More data for this Ligand-Target Pair