TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 480nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 590nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 620nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 690nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 870nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 880nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 930nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 940nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 1.02E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 1.12E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 1.18E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 1.41E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 1.92E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 2.12E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 2.90E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 2.95E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 3.35E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 3.95E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 4.00E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 4.20E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 4.55E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 4.85E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 5.09E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 5.90E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 6.20E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 8.50E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
TargetPeptidyl-prolyl cis-trans isomerase A(Rattus norvegicus)
Guilford Pharmaceuticals
Curated by ChEMBL
Guilford Pharmaceuticals
Curated by ChEMBL
Affinity DataIC50: 9.50E+3nMAssay Description:In vitro inhibition of the rotamase activity of cyclophilin A (CyPA)More data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+5nMAssay Description:In vitro inhibitory activity against binding of Selectin E to human recombinant AGP (alpha-1 acid glycoprotein) containing sLex derivativeMore data for this Ligand-Target Pair
Affinity DataIC50: 1.60E+6nMAssay Description:In vitro inhibitory activity against Selectin E binding to human recombinant AGP (alpha-1 acid glycoprotein)More data for this Ligand-Target Pair
Affinity DataIC50: 2.50E+6nMAssay Description:Ability to inhibit the binding of P-selectin glycoprotein ligand 1 (PSGL-1) fusion protein to immobilized soluble P-selectin in a P-selectin assay.More data for this Ligand-Target Pair
Affinity DataIC50: 3.00E+6nMAssay Description:In vitro inhibitory activity against Selectin E binding to human recombinant AGP (alpha-1 acid glycoprotein)More data for this Ligand-Target Pair
Affinity DataIC50: 5.00E+6nMAssay Description:Ability to inhibit the binding of E-selectin to human recombinant AGP (alpha-1 acid glycoprotein) in a E-selectin assayMore data for this Ligand-Target Pair
Affinity DataIC50: 6.00E+6nMAssay Description:In vitro inhibitory activity against Selectin E binding to human recombinant AGP (alpha-1 acid glycoprotein)More data for this Ligand-Target Pair
Affinity DataIC50: 6.00E+6nMAssay Description:In vitro inhibitory activity against Selectin E binding to human recombinant AGP (alpha-1 acid glycoprotein)More data for this Ligand-Target Pair
Affinity DataIC50: 6.70E+6nMAssay Description:In vitro inhibitory activity against Selectin E binding to human recombinant AGP (alpha-1 acid glycoprotein)More data for this Ligand-Target Pair
Affinity DataIC50: 7.00E+6nMAssay Description:In vitro inhibitory activity against Selectin E binding to human recombinant AGP (alpha-1 acid glycoprotein)More data for this Ligand-Target Pair
Affinity DataIC50: 7.00E+6nMAssay Description:In vitro inhibitory activity against Selectin E binding to human recombinant AGP (alpha-1 acid glycoprotein)More data for this Ligand-Target Pair
Affinity DataIC50: 8.00E+6nMAssay Description:In vitro inhibitory activity against Selectin E binding to human recombinant AGP (alpha-1 acid glycoprotein)More data for this Ligand-Target Pair
Affinity DataIC50: 8.00E+6nMAssay Description:Ability to inhibit the binding of E-selectin to human recombinant AGP (alpha-1 acid glycoprotein) in a E-selectin assayMore data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:In vitro inhibitory activity against Selectin E binding to human recombinant AGP (alpha-1 acid glycoprotein)More data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+7nMAssay Description:Inhibitory concentration against selectin P in Biacore assayMore data for this Ligand-Target Pair
Affinity DataIC50: 1.00E+7nMAssay Description:In vitro inhibitory activity against Selectin E binding to human recombinant AGP (alpha-1 acid glycoprotein)More data for this Ligand-Target Pair
Affinity DataIC50: >1.00E+7nMAssay Description:In vitro inhibitory activity against Selectin E binding to human recombinant AGP (alpha-1 acid glycoprotein)More data for this Ligand-Target Pair
Affinity DataIC50: 2.50E+8nMAssay Description:Ability to inhibit the binding of P-selectin glycoprotein ligand 1 (PSGL-1) fusion protein to immobilized soluble P-selectin in a P-selectin assay.More data for this Ligand-Target Pair