Affinity DataKi: 0.106nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.140nMAssay Description:Compound was evaluated for their ability to inhibit the alpha-thrombin-mediated hydrolysis of the fluorescent substrate Tos-Gly-Pro-Arg-AmcMore data for this Ligand-Target Pair
Affinity DataKi: 0.350nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.370nMAssay Description:Compound was evaluated for their ability to inhibit the alpha-thrombin-mediated hydrolysis of the fluorescent substrate Tos-Gly-Pro-Arg-AmcMore data for this Ligand-Target Pair
Affinity DataKi: 0.5nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.5nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.5nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.5nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.560nMAssay Description:Compound was evaluated for their ability to inhibit the alpha-thrombin-mediated hydrolysis of the fluorescent substrate Tos-Gly-Pro-Arg-AmcMore data for this Ligand-Target Pair
Affinity DataKi: 0.600nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 0.920nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 1.20nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 2nMAssay Description:In vitro inhibitory activity against human thrombin.( Fast moving component on HPLC)More data for this Ligand-Target Pair
Affinity DataKi: 2.20nMAssay Description:Inhibition of binding of [3H]naloxone to Opioid receptor mu 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 2.30nMAssay Description:Inhibition of binding of [3H]naloxone to Opioid receptor mu 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 2.5nMAssay Description:Inhibition of binding of [3H]naloxone to Opioid receptor mu 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 2.5nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 2.80nMAssay Description:Compound was evaluated for their ability to inhibit the alpha-thrombin-mediated hydrolysis of the fluorescent substrate Tos-Gly-Pro-Arg-AmcMore data for this Ligand-Target Pair
Affinity DataKi: 3nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 3nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 3.10nMAssay Description:Inhibition of binding of [3H]naloxone to Opioid receptor mu 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 3.10nMAssay Description:Inhibition of [3H][D-Ala2,D-Leu5]enkephalin binding to Opioid receptor delta 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 3.20nMAssay Description:Compound was evaluated for their ability to inhibit the alpha-thrombin-mediated hydrolysis of the fluorescent substrate Tos-Gly-Pro-Arg-AmcMore data for this Ligand-Target Pair
Affinity DataKi: 3.30nMAssay Description:Inhibition of binding of [3H]naloxone to Opioid receptor mu 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 3.5nMAssay Description:Compound was evaluated for their ability to inhibit the alpha-thrombin-mediated hydrolysis of the fluorescent substrate Tos-Gly-Pro-Arg-AmcMore data for this Ligand-Target Pair
Affinity DataKi: 3.80nMAssay Description:Compound was evaluated for their ability to inhibit the alpha-thrombin-mediated hydrolysis of the fluorescent substrate Tos-Gly-Pro-Arg-AmcMore data for this Ligand-Target Pair
Affinity DataKi: 4.10nMAssay Description:Inhibition of binding of [3H]naloxone to Opioid receptor mu 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 4.40nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 4.40nMAssay Description:Inhibition of [3H][D-Ala2,D-Leu5]enkephalin binding to Opioid receptor delta 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 4.70nMAssay Description:Inhibition of binding of [3H]naloxone to Opioid receptor mu 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 5nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 5.60nMAssay Description:Inhibition of binding of [3H]naloxone to Opioid receptor mu 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 6nMAssay Description:In vitro inhibitory activity against human thrombin.(Slow moving component on HPLC)More data for this Ligand-Target Pair
Affinity DataKi: 8nMAssay Description:In vitro inhibitory activity against human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 10nMAssay Description:In vitro inhibitory activity against human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 12nMAssay Description:Inhibition of binding of [3H]naloxone to Opioid receptor mu 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 14nMAssay Description:Inhibition of binding of [3H]naloxone to Opioid receptor mu 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 15nMAssay Description:Inhibition of [3H][D-Ala2,D-Leu5]enkephalin binding to Opioid receptor delta 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 16nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 16nMAssay Description:In vitro inhibitory activity against human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 17nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 18nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 18nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 18nMAssay Description:In vitro inhibitory activity against human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 18nMAssay Description:In vitro inhibitory activity against human thrombin.More data for this Ligand-Target Pair
Affinity DataKi: 22nMAssay Description:Inhibition of [3H][D-Ala2,D-Leu5]enkephalin binding to Opioid receptor delta 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 24nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 25nMAssay Description:Binding affinity of the compound against thrombinMore data for this Ligand-Target Pair
Affinity DataKi: 27.7nMAssay Description:Inhibition of [3H][D-Ala2,D-Leu5]enkephalin binding to Opioid receptor delta 1 in the rat brain homogenateMore data for this Ligand-Target Pair
Affinity DataKi: 28nMAssay Description:Inhibition of binding of [3H]naloxone to Opioid receptor mu 1 in the rat brain homogenateMore data for this Ligand-Target Pair