Affinity DataIC50: 1.81E+3nMAssay Description:Inhibition of factor 5a-mediated prothrombin activation in human plasma by prothrombinase assayMore data for this Ligand-Target Pair
Affinity DataIC50: 2.50E+3nMAssay Description:Inhibition of human factor 5a light chain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 3.51E+3nMAssay Description:Inhibition of human recombinant factor 5a C2 domain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 3.80E+3nMAssay Description:Inhibition of factor 5a-mediated prothrombin activation in human plasma by prothrombinase assayMore data for this Ligand-Target Pair
Affinity DataIC50: 4.80E+3nMAssay Description:Inhibition of human factor 5a light chain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 5.53E+3nMAssay Description:Inhibition of human recombinant factor 5a C2 domain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 6.71E+3nMAssay Description:Inhibition of human recombinant factor 5a C2 domain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 7.40E+3nMAssay Description:Inhibition of human recombinant factor 5a C2 domain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 7.80E+3nMAssay Description:Inhibition of human factor 8 binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 8.55E+3nMAssay Description:Inhibition of human factor 5a light chain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 8.56E+3nMAssay Description:Inhibition of human factor 5a light chain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 8.90E+3nMAssay Description:Inhibition of human factor 8 binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 8.95E+3nMAssay Description:Inhibition of factor 5a-mediated prothrombin activation in human plasma by prothrombinase assayMore data for this Ligand-Target Pair
Affinity DataIC50: 9.19E+3nMAssay Description:Inhibition of factor 5a-mediated prothrombin activation in human plasma by prothrombinase assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.40E+4nMAssay Description:Inhibition of human recombinant factor 5a C2 domain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.41E+4nMAssay Description:Inhibition of human factor 5a light chain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.41E+4nMAssay Description:Inhibition of human factor 5a light chain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.50E+4nMAssay Description:Binding affinity at mouse EphB2 receptor by ELISAMore data for this Ligand-Target Pair
Affinity DataIC50: 1.57E+4nMAssay Description:Inhibition of human factor 5a light chain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.64E+4nMAssay Description:Inhibition of human recombinant factor 5a C2 domain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.86E+4nMAssay Description:Inhibition of factor 5a-mediated prothrombin activation in human plasma by prothrombinase assayMore data for this Ligand-Target Pair
Affinity DataIC50: 2.19E+4nMAssay Description:Inhibition of human recombinant factor 5a C2 domain binding to immobilized phospholipid by surface plasmon resonance assayMore data for this Ligand-Target Pair
Affinity DataIC50: 3.24E+4nMAssay Description:Inhibition of factor 5a-mediated prothrombin activation in human plasma by prothrombinase assayMore data for this Ligand-Target Pair
Affinity DataIC50: 3.81E+4nMAssay Description:Inhibition of factor 5a-mediated prothrombin activation in human plasma by prothrombinase assayMore data for this Ligand-Target Pair
Affinity DataIC50: 4.06E+4nMAssay Description:Inhibition of factor 5a-mediated prothrombin activation in human plasma by prothrombinase assayMore data for this Ligand-Target Pair
Affinity DataIC50: 6.29E+4nMAssay Description:Inhibition of factor 5a-mediated prothrombin activation in human plasma by prothrombinase assayMore data for this Ligand-Target Pair
Affinity DataKd: 6.00E+3nMAssay Description:Binding affinity at human EphB2 receptor by isothermal titration calorimetryMore data for this Ligand-Target Pair
Affinity DataKd: >5.00E+4nMAssay Description:Binding affinity at human EphB2 receptor by isothermal titration calorimetryMore data for this Ligand-Target Pair
Affinity DataKd: >5.00E+4nMAssay Description:Binding affinity at human EphB2 receptor by isothermal titration calorimetryMore data for this Ligand-Target Pair
Affinity DataKd: >5.00E+4nMAssay Description:Binding affinity at human EphB2 receptor by isothermal titration calorimetryMore data for this Ligand-Target Pair
Affinity DataKd: >5.00E+4nMAssay Description:Binding affinity at human EphB2 receptor by isothermal titration calorimetryMore data for this Ligand-Target Pair
Affinity DataKd: >5.00E+4nMAssay Description:Binding affinity at human EphB2 receptor by isothermal titration calorimetryMore data for this Ligand-Target Pair
Affinity DataKd: >5.00E+4nMAssay Description:Binding affinity at human EphB2 receptor by isothermal titration calorimetryMore data for this Ligand-Target Pair
Affinity DataKd: 6.00E+3nMAssay Description:Binding affinity at human EphB2 receptor by isothermal titration calorimetryMore data for this Ligand-Target Pair
Affinity DataKd: 3.00E+3nMAssay Description:Binding affinity at human EphB2 receptor by isothermal titration calorimetryMore data for this Ligand-Target Pair
Affinity DataKd: 1.10E+4nMAssay Description:Binding affinity at human EphB2 receptor by isothermal titration calorimetryMore data for this Ligand-Target Pair
Affinity DataKd: >5.00E+4nMAssay Description:Binding affinity at human EphB2 receptor by isothermal titration calorimetryMore data for this Ligand-Target Pair
Target5'-AMP-activated protein kinase catalytic subunit alpha-1/subunit beta-1/subunit gamma-1(Homo sapiens (Human))
Maastricht University
Curated by ChEMBL
Maastricht University
Curated by ChEMBL
Affinity DataKd: 510nMAssay Description:Binding affinity to human recombinant N-terminal AVI-tagged phosphorylated AMPK alpha1beta1gamma1 expressed in Escherichia coli BL21 cells after 1 to...More data for this Ligand-Target Pair
Target5'-AMP-activated protein kinase catalytic subunit alpha-1/subunit beta-2/subunit gamma-1(Homo sapiens (Human))
Maastricht University
Curated by ChEMBL
Maastricht University
Curated by ChEMBL
Affinity DataKd: 1.45E+4nMAssay Description:Binding affinity to human recombinant N-terminal AVI-tagged phosphorylated AMPK alpha1beta2gamma1 expressed in Escherichia coli BL21 cells after 1 to...More data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 14(Mus musculus (mouse))
King'S College London
Curated by ChEMBL
King'S College London
Curated by ChEMBL
Affinity DataKd: 2.51E+4nMAssay Description:Binding affinity to 6x-His tagged mouse recombinant p38alpha expressed in Escherichia coli Rosetta 2 (Novagen) cells by ITC analysisMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 14(Mus musculus (mouse))
King'S College London
Curated by ChEMBL
King'S College London
Curated by ChEMBL
Affinity DataKd: 5.78E+4nMAssay Description:Binding affinity to 6x-His tagged mouse recombinant p38alpha expressed in Escherichia coli Rosetta 2 (Novagen) cells by ITC analysisMore data for this Ligand-Target Pair
TargetMitogen-activated protein kinase 14(Mus musculus (mouse))
King'S College London
Curated by ChEMBL
King'S College London
Curated by ChEMBL
Affinity DataKd: 1.12E+5nMAssay Description:Binding affinity to 6x-His tagged mouse recombinant p38alpha expressed in Escherichia coli Rosetta 2 (Novagen) cells by ITC analysisMore data for this Ligand-Target Pair
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
Queen Mary University Of London
Curated by ChEMBL
Queen Mary University Of London
Curated by ChEMBL
Affinity DataEC50: 250nMAssay Description:Agonist activity at FPRL1 (unknown origin) expressed in CHO-K1 cells assessed as increase in calcium mobilization incubated for 2.5 hrs by cellular b...More data for this Ligand-Target Pair
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
Queen Mary University Of London
Curated by ChEMBL
Queen Mary University Of London
Curated by ChEMBL
Affinity DataEC50: 350nMAssay Description:Agonist activity at FPRL1 (unknown origin) expressed in CHO-K1 cells assessed as increase in calcium mobilization incubated for 2.5 hrs by cellular b...More data for this Ligand-Target Pair
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
Queen Mary University Of London
Curated by ChEMBL
Queen Mary University Of London
Curated by ChEMBL
Affinity DataEC50: 2.70E+3nMAssay Description:Agonist activity at FPRL1 (unknown origin) expressed in CHO-K1 cells assessed as increase in calcium mobilization incubated for 2.5 hrs by cellular b...More data for this Ligand-Target Pair
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
Queen Mary University Of London
Curated by ChEMBL
Queen Mary University Of London
Curated by ChEMBL
Affinity DataEC50: 2.70E+3nMAssay Description:Agonist activity at FPRL1 (unknown origin) expressed in CHO-K1 cells assessed as increase in calcium mobilization incubated for 2.5 hrs by cellular b...More data for this Ligand-Target Pair
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
Queen Mary University Of London
Curated by ChEMBL
Queen Mary University Of London
Curated by ChEMBL
Affinity DataEC50: 130nMAssay Description:Agonist activity at FPRL1 (unknown origin) expressed in CHO-K1 cells assessed as increase in calcium mobilization incubated for 2.5 hrs by cellular b...More data for this Ligand-Target Pair
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
Queen Mary University Of London
Curated by ChEMBL
Queen Mary University Of London
Curated by ChEMBL
Affinity DataEC50: 130nMAssay Description:Agonist activity at FPRL1 (unknown origin) expressed in CHO-K1 cells assessed as increase in calcium mobilization incubated for 2.5 hrs by cellular b...More data for this Ligand-Target Pair
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
Queen Mary University Of London
Curated by ChEMBL
Queen Mary University Of London
Curated by ChEMBL
Affinity DataEC50: 280nMAssay Description:Agonist activity at FPRL1 (unknown origin) expressed in CHO-K1 cells assessed as increase in calcium mobilization incubated for 2.5 hrs by cellular b...More data for this Ligand-Target Pair
TargetN-formyl peptide receptor 2(Homo sapiens (Human))
Queen Mary University Of London
Curated by ChEMBL
Queen Mary University Of London
Curated by ChEMBL
Affinity DataEC50: 8nMAssay Description:Agonist activity at FPRL1 (unknown origin) expressed in CHO-K1 cells assessed as increase in calcium mobilization incubated for 2.5 hrs by cellular b...More data for this Ligand-Target Pair