TargetMu-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 0.0420nMAssay Description:Compound was tested for Opioid receptor mu 1 agonism in isolated tissues from guinea pig ileumMore data for this Ligand-Target Pair
TargetMu-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 0.114nMAssay Description:Compound was tested for binding affinity towards Opioid receptor mu 1 by displacing [3H]DAGO radioligand in rat brain P2 synaptosomes membranes.More data for this Ligand-Target Pair
TargetMu-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 0.115nMAssay Description:Compound was tested for Opioid receptor mu 1 agonism in isolated tissues from guinea pig ileumMore data for this Ligand-Target Pair
TargetMu-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 1.20nMAssay Description:Compound was tested for binding affinity towards Opioid receptor mu 1 by displacing [3H]DAGO radioligand in rat brain P2 synaptosomes membranes.More data for this Ligand-Target Pair
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 7.30nMAssay Description:Compound was tested for binding affinity towards opioid receptor delta 1 by displacing [3H]DPDPE radioligand in rat brain P2 synaptosomes membranes.More data for this Ligand-Target Pair
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 13nMAssay Description:pA2 is the negative log of the molar concentration required to double the agonism of opioid receptor delta 1More data for this Ligand-Target Pair
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 16nMAssay Description:Compound was tested for binding affinity towards opioid receptor delta 1 by displacing [3H]DPDPE radioligand in rat brain P2 synaptosomes membranes.More data for this Ligand-Target Pair
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 23nMAssay Description:Compound was tested for Opioid receptor mu 1 agonism in isolated tissues from guinea pig ileumMore data for this Ligand-Target Pair
TargetMu-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 26nMAssay Description:Compound was tested for binding affinity towards Opioid receptor mu 1 by displacing [3H]DAGO radioligand in rat brain P2 synaptosomes membranes.More data for this Ligand-Target Pair
TargetMu-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 70nMAssay Description:Compound was tested for binding affinity towards Opioid receptor mu 1 by displacing [3H]DAGO radioligand in rat brain P2 synaptosomes membranes.More data for this Ligand-Target Pair
TargetMu-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 309nMAssay Description:Compound was tested for binding affinity towards Opioid receptor mu 1 by displacing [3H]DAGO radioligand in rat brain P2 synaptosomes membranes.More data for this Ligand-Target Pair
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 435nMAssay Description:Compound was tested for binding affinity towards opioid receptor delta 1 by displacing [3H]DPDPE radioligand in rat brain P2 synaptosomes membranes.More data for this Ligand-Target Pair
TargetMu-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 460nMAssay Description:Compound was tested for binding affinity towards Opioid receptor mu 1 by displacing [3H]DAGO radioligand in rat brain P2 synaptosomes membranes.More data for this Ligand-Target Pair
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 1.83E+3nMAssay Description:Compound was tested for binding affinity towards opioid receptor delta 1 by displacing [3H]DPDPE radioligand in rat brain P2 synaptosomes membranes.More data for this Ligand-Target Pair
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 2.19E+3nMAssay Description:Compound was tested for binding affinity towards opioid receptor delta 1 by displacing [3H]DPDPE radioligand in rat brain P2 synaptosomes membranes.More data for this Ligand-Target Pair
TargetDelta-type opioid receptor(Rattus norvegicus (rat))
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataKi: 2.90E+3nMAssay Description:Compound was tested for binding affinity towards opioid receptor delta 1 by displacing [3H]DPDPE radioligand in rat brain P2 synaptosomes membranes.More data for this Ligand-Target Pair
Affinity DataIC50: 0.210nMAssay Description:Ability to inhibit binding of biotin-labeled human fibrinogen to immobilized fibrinogen receptor purified from human erythroleukemia(HEL) cells.More data for this Ligand-Target Pair
Affinity DataIC50: 0.290nMAssay Description:Ability to inhibit binding of biotin-labeled human fibrinogen to immobilized fibrinogen receptor purified from human erythroleukemia(HEL) cells.More data for this Ligand-Target Pair
Affinity DataIC50: 0.420nMAssay Description:Ability to inhibit binding of biotin-labeled human fibrinogen to immobilized fibrinogen receptor purified from human erythroleukemia(HEL) cells.More data for this Ligand-Target Pair
Affinity DataIC50: 0.740nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 0.890nMAssay Description:Ability to inhibit binding of biotin-labeled human fibrinogen to immobilized fibrinogen receptor purified from human erythroleukemia(HEL) cells.More data for this Ligand-Target Pair
Affinity DataIC50: 0.910nMAssay Description:Ability to inhibit binding of biotin-labeled human fibrinogen to immobilized fibrinogen receptor purified from human erythroleukemia(HEL) cells.More data for this Ligand-Target Pair
Affinity DataIC50: 0.920nMAssay Description:Ability to inhibit binding of biotin-labeled human fibrinogen to immobilized fibrinogen receptor purified from human erythroleukemia(HEL) cells.More data for this Ligand-Target Pair
Affinity DataIC50: 0.950nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 0.950nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 0.970nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 1nMAssay Description:Ability to inhibit binding of biotin-labeled human fibrinogen to immobilized fibrinogen receptor purified from human erythroleukemia(HEL) cells.More data for this Ligand-Target Pair
Affinity DataIC50: 1nMAssay Description:Ability to inhibit binding of biotin-labeled human fibrinogen to immobilized fibrinogen receptor purified from human erythroleukemia(HEL) cells.More data for this Ligand-Target Pair
Affinity DataIC50: 1nMAssay Description:Ability to inhibit binding of biotin-labeled human fibrinogen to immobilized fibrinogen receptor purified from human erythroleukemia(HEL) cells.More data for this Ligand-Target Pair
TargetMu-type opioid receptor(GUINEA PIG)
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataIC50: 1.30nMAssay Description:Compound was tested for Opioid receptor mu 1 agonism in isolated tissues from guinea pig ileumMore data for this Ligand-Target Pair
Affinity DataIC50: 1.40nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 1.60nMAssay Description:Ability to inhibit binding of biotin-labeled human fibrinogen to immobilized fibrinogen receptor purified from human erythroleukemia(HEL) cells.More data for this Ligand-Target Pair
Affinity DataIC50: 1.90nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
TargetMu-type opioid receptor(GUINEA PIG)
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
National Institutes Of Environmental Health Sciences
Curated by ChEMBL
Affinity DataIC50: 1.90nMAssay Description:Compound was tested for Opioid receptor mu 1 agonism in isolated tissues from guinea pig ileumMore data for this Ligand-Target Pair
Affinity DataIC50: 2nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 2nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 2nMAssay Description:Compound was measured for inhibition of collagenolytic of human Cathepsin LMore data for this Ligand-Target Pair
Affinity DataIC50: 2nMAssay Description:Ability to inhibit binding of biotin-labeled human fibrinogen to immobilized fibrinogen receptor purified from human erythroleukemia(HEL) cells.More data for this Ligand-Target Pair
Affinity DataIC50: 2.10nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 2.20nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 2.20nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 2.20nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 2.20nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 2.5nMAssay Description:Ability to inhibit binding of biotin-labeled human fibrinogen to immobilized fibrinogen receptor purified from human erythroleukemia(HEL) cells.More data for this Ligand-Target Pair
Affinity DataIC50: 2.5nMAssay Description:Compound was measured for inhibition of collagenolytic of human Cathepsin LMore data for this Ligand-Target Pair
Affinity DataIC50: 3.10nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 3.30nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 3.30nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 3.90nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair
Affinity DataIC50: 4.30nMAssay Description:Inhibition of human cathepsin L.More data for this Ligand-Target Pair