Report error Found 9156 with Last Name = 'lu' and Initial = 'x'
Affinity DataKd: 2.43E+4nMpH: 7.4 T: 2°CAssay Description:CypA in vitro were determined by employing surface plasmon resonance (SPR) technology. More data for this Ligand-Target Pair
Affinity DataKd: 3.07E+3nMpH: 7.4 T: 2°CAssay Description:CypA in vitro were determined by employing surface plasmon resonance (SPR) technology. More data for this Ligand-Target Pair
Affinity DataKd: 212nMpH: 7.4 T: 2°CAssay Description:CypA in vitro were determined by employing surface plasmon resonance (SPR) technology. More data for this Ligand-Target Pair
Affinity DataKd: 1.72E+4nMpH: 7.4 T: 2°CAssay Description:CypA in vitro were determined by employing surface plasmon resonance (SPR) technology. More data for this Ligand-Target Pair
Affinity DataKd: 3.41E+3nMpH: 7.4 T: 2°CAssay Description:CypA in vitro were determined by employing surface plasmon resonance (SPR) technology. More data for this Ligand-Target Pair
Affinity DataKd: 76.2nMpH: 7.4 T: 2°CAssay Description:CypA in vitro were determined by employing surface plasmon resonance (SPR) technology. More data for this Ligand-Target Pair
Affinity DataKd: 2.88E+4nMpH: 7.4 T: 2°CAssay Description:CypA in vitro were determined by employing surface plasmon resonance (SPR) technology. More data for this Ligand-Target Pair
Affinity DataKd: 8.18E+3nMpH: 7.4 T: 2°CAssay Description:CypA in vitro were determined by employing surface plasmon resonance (SPR) technology. More data for this Ligand-Target Pair
Affinity DataKd: 1.08E+4nMpH: 7.4 T: 2°CAssay Description:CypA in vitro were determined by employing surface plasmon resonance (SPR) technology. More data for this Ligand-Target Pair
Affinity DataKd: 2.73E+4nMpH: 7.4 T: 2°CAssay Description:CypA in vitro were determined by employing surface plasmon resonance (SPR) technology. More data for this Ligand-Target Pair
Affinity DataKd: 3.08E+4nMpH: 7.4 T: 2°CAssay Description:CypA in vitro were determined by employing surface plasmon resonance (SPR) technology. More data for this Ligand-Target Pair
TargetProtein arginine N-methyltransferase 3(Human)
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Affinity DataEC50: 5.20E+3nMAssay Description:Binding affinity to beta galactosidase fused human PRMT3 (211 to 531 residues) expressed in human HEK293 cells after 6 hrs by InCELL hunter assayMore data for this Ligand-Target Pair
TargetProtein arginine N-methyltransferase 3(Human)
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Affinity DataEC50: 2.70E+3nMAssay Description:Binding affinity to beta galactosidase fused human PRMT3 (211 to 531 residues) expressed in human HEK293 cells after 6 hrs by InCELL hunter assayMore data for this Ligand-Target Pair
TargetProtein arginine N-methyltransferase 3(Human)
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Affinity DataEC50: 1.80E+3nMAssay Description:Binding affinity to beta galactosidase fused human PRMT3 (211 to 531 residues) expressed in human HEK293 cells after 6 hrs by InCELL hunter assayMore data for this Ligand-Target Pair
TargetProtein arginine N-methyltransferase 3(Human)
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Affinity DataEC50: 4.90E+3nMAssay Description:Binding affinity to beta galactosidase fused human PRMT3 (211 to 531 residues) expressed in human A549 cells after 6 hrs by InCELL hunter assayMore data for this Ligand-Target Pair
TargetProtein arginine N-methyltransferase 3(Human)
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Affinity DataEC50: 1.60E+3nMAssay Description:Binding affinity to beta galactosidase fused human PRMT3 (211 to 531 residues) expressed in human A549 cells after 6 hrs by InCELL hunter assayMore data for this Ligand-Target Pair
TargetProtein arginine N-methyltransferase 3(Human)
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Affinity DataEC50: 2.00E+3nMAssay Description:Binding affinity to beta galactosidase fused human PRMT3 (211 to 531 residues) expressed in human A549 cells after 6 hrs by InCELL hunter assayMore data for this Ligand-Target Pair
TargetProtein arginine N-methyltransferase 3(Human)
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Affinity DataEC50: 3.10E+3nMAssay Description:Binding affinity to beta galactosidase fused human PRMT3 (211 to 531 residues) expressed in human HEK293 cells after 6 hrs by InCELL hunter assayMore data for this Ligand-Target Pair
TargetProtein arginine N-methyltransferase 3(Human)
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Icahn School of Medicine At Mount Sinai
Curated by ChEMBL
Affinity DataEC50: 2.70E+3nMAssay Description:Binding affinity to beta galactosidase fused human PRMT3 (211 to 531 residues) expressed in human A549 cells after 6 hrs by InCELL hunter assayMore data for this Ligand-Target Pair
Affinity DataKd: 283nMAssay Description:Binding affinity to human recombinant UbcH5c by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKd: 6.40E+3nMAssay Description:Binding affinity to human recombinant UbcH5c by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKd: 2.58E+3nMAssay Description:Binding affinity to human recombinant UbcH5c by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKd: 3.64E+3nMAssay Description:Binding affinity to human recombinant UbcH5c by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKd: 353nMAssay Description:Binding affinity to human recombinant UbcH5c by SPR analysisMore data for this Ligand-Target Pair
Affinity DataKd: 2.20nMAssay Description:Binding affinity to human DNA-tagged DDR1 expressed in bacterial expression system measured after 1 hr by quantitative PCR analysisMore data for this Ligand-Target Pair
TargetDual specificity mitogen-activated protein kinase kinase 5(Human)
University of Macau
Curated by ChEMBL
University of Macau
Curated by ChEMBL
Affinity DataKd: 88nMAssay Description:Binding affinity to partial length human MEK5 expressed in HEK293 cells by active-site-dependent competition assayMore data for this Ligand-Target Pair
Affinity DataKd: 45nMAssay Description:Binding affinity to partial length human SIK expressed in Escherichia coli BL21 by active-site-dependent competition assayMore data for this Ligand-Target Pair
Affinity DataKd: 64nMAssay Description:Binding affinity to partial length human SRMS expressed in HEK293 cells by active-site-dependent competition assayMore data for this Ligand-Target Pair
Affinity DataKd: 460nMAssay Description:Binding affinity to partial length human KIT expressed in Escherichia coli BL21 by active-site-dependent competition assayMore data for this Ligand-Target Pair
Affinity DataKd: 22nMAssay Description:Binding affinity to partial length human FRK expressed in Escherichia coli BL21 by active-site-dependent competition assayMore data for this Ligand-Target Pair
Affinity DataKd: 2.70nMAssay Description:Binding affinity to partial length human ZAK expressed in Escherichia coli BL21 by active-site-dependent competition assayMore data for this Ligand-Target Pair
Affinity DataKd: 64nMAssay Description:Binding affinity to partial length human AURKB expressed in HEK293 cells by active-site-dependent competition assayMore data for this Ligand-Target Pair
Affinity DataKd: 370nMAssay Description:Binding affinity to human TIE2More data for this Ligand-Target Pair
Affinity DataKd: 260nMAssay Description:Binding affinity to human EPHA2More data for this Ligand-Target Pair
Affinity DataKd: 180nMAssay Description:Binding affinity to human LCKMore data for this Ligand-Target Pair
Affinity DataKd: 9.30nMAssay Description:Binding affinity to human TrkCMore data for this Ligand-Target Pair
Affinity DataKd: 7.90nMAssay Description:Binding affinity to human DDR1More data for this Ligand-Target Pair
Affinity DataKd: 8nMAssay Description:Binding affinity to human DDR2More data for this Ligand-Target Pair
Affinity DataKd: 200nMAssay Description:Binding affinity to human EPHA7More data for this Ligand-Target Pair
Affinity DataKd: 79nMAssay Description:Binding affinity to human EPHA8More data for this Ligand-Target Pair
Affinity DataKd: 260nMAssay Description:Binding affinity to human EPHB2More data for this Ligand-Target Pair
Affinity DataKd: 10nMAssay Description:Binding affinity to human LOKMore data for this Ligand-Target Pair
Affinity DataKd: 100nMAssay Description:Binding affinity to human TrkAMore data for this Ligand-Target Pair
Affinity DataKd: 11nMAssay Description:Binding affinity to human TrkBMore data for this Ligand-Target Pair
Affinity DataKd: 9.40E+3nMAssay Description:Binding affinity to VBC complex (unknown origin) by ITC assayMore data for this Ligand-Target Pair
Affinity DataKd: 1.00E+3nMAssay Description:Binding affinity to VBC complex (unknown origin) assessed as reduction of FAM-labelled HIF1alpha peptide binding by fluorescence polarization assayMore data for this Ligand-Target Pair
Affinity DataKd: >1.30E+4nMAssay Description:Binding affinity to VBC complex (unknown origin) assessed as reduction of FAM-labelled HIF1alpha peptide binding by fluorescence polarization assayMore data for this Ligand-Target Pair
Affinity DataKd: 440nMAssay Description:Binding affinity to VBC complex (unknown origin) by ITC assayMore data for this Ligand-Target Pair
Affinity DataKd: 2.16E+4nMAssay Description:Binding affinity to VBC complex (unknown origin) by ITC assayMore data for this Ligand-Target Pair
Affinity DataKd: 690nMAssay Description:Binding affinity to VBC complex (unknown origin) assessed as reduction of FAM-labelled HIF1alpha peptide binding by fluorescence polarization assayMore data for this Ligand-Target Pair
