TargetTyrosine-protein kinase receptor(Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
TargetTyrosine-protein kinase receptor(Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
TargetTyrosine-protein kinase receptor(Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
TargetTyrosine-protein kinase receptor(Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
TargetALK tyrosine kinase receptor [L1196M](Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
TargetALK tyrosine kinase receptor [L1196M](Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
TargetALK tyrosine kinase receptor [L1196M](Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
TargetALK tyrosine kinase receptor [G1269S](Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
TargetALK tyrosine kinase receptor [G1269S](Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
TargetALK tyrosine kinase receptor [G1269S](Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
TargetBcl2-associated agonist of cell death(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 970nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-XlMore data for this Ligand-Target Pair
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 1.30E+3nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-wMore data for this Ligand-Target Pair
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 1.70E+3nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl2More data for this Ligand-Target Pair
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 2.20E+3nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-wMore data for this Ligand-Target Pair
TargetBcl2-associated agonist of cell death(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 2.30E+3nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-XlMore data for this Ligand-Target Pair
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 2.30E+3nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-wMore data for this Ligand-Target Pair
TargetBcl2-associated agonist of cell death(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 2.40E+3nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-XlMore data for this Ligand-Target Pair
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 4.30E+3nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl2More data for this Ligand-Target Pair
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 4.30E+3nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl2More data for this Ligand-Target Pair
TargetBcl2-associated agonist of cell death(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 5.25E+3nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-XlMore data for this Ligand-Target Pair
TargetBcl2-associated agonist of cell death(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 8.70E+3nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-XlMore data for this Ligand-Target Pair
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 1.37E+4nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-wMore data for this Ligand-Target Pair
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 1.42E+4nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl2More data for this Ligand-Target Pair
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 2.12E+4nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl2More data for this Ligand-Target Pair
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 2.15E+4nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-wMore data for this Ligand-Target Pair
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 3.92E+4nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-wMore data for this Ligand-Target Pair
TargetBcl2-associated agonist of cell death(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 5.84E+4nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-XlMore data for this Ligand-Target Pair
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 8.83E+4nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-wMore data for this Ligand-Target Pair
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 9.90E+4nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-wMore data for this Ligand-Target Pair
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 1.01E+5nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-wMore data for this Ligand-Target Pair
TargetBcl2-associated agonist of cell death(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 1.04E+5nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-XlMore data for this Ligand-Target Pair
TargetBcl2-associated agonist of cell death(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 1.12E+5nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-XlMore data for this Ligand-Target Pair
TargetBcl-2-like protein 2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 1.16E+5nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-wMore data for this Ligand-Target Pair
TargetBcl2-associated agonist of cell death(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 1.34E+5nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-XlMore data for this Ligand-Target Pair
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 1.61E+5nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl2More data for this Ligand-Target Pair
TargetBcl2-associated agonist of cell death(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 1.76E+5nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl-XlMore data for this Ligand-Target Pair
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 2.26E+5nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl2More data for this Ligand-Target Pair
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 2.43E+5nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl2More data for this Ligand-Target Pair
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: 2.60E+5nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl2More data for this Ligand-Target Pair
TargetApoptosis regulator Bcl-2(Homo sapiens (Human))
University Of Minnesota Minneapolis
Curated by ChEMBL
University Of Minnesota Minneapolis
Curated by ChEMBL
Affinity DataKi: >1.00E+6nMAssay Description:Inhibition of Bak peptide binding to human recombinant Bcl2More data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
Affinity DataIC50: 0.100nMAssay Description:EGFR, EGFR (T790M, L858R), HER2 kinase were expressed and purified through an insect cell expression system by the Department of Biology, Centaurus B...More data for this Ligand-Target Pair
TargetHigh affinity nerve growth factor receptor [G667C](Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
Affinity DataIC50: 0.120nMAssay Description:TrkAG667C (Kinase domain) kinase was expressed in Sf9 cells by using pIEX-Bac-4, and purified by using affinity chromatography on AKTA Purifier (GE c...More data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
Affinity DataIC50: 0.200nMAssay Description:EGFR, EGFR (T790M, L858R), HER2 kinase were expressed and purified through an insect cell expression system by the Department of Biology, Centaurus B...More data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
Affinity DataIC50: 0.200nMAssay Description:EGFR, EGFR (T790M, L858R), HER2 kinase were expressed and purified through an insect cell expression system by the Department of Biology, Centaurus B...More data for this Ligand-Target Pair
TargetEpidermal growth factor receptor(Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
Affinity DataIC50: 0.200nMAssay Description:EGFR, EGFR (T790M, L858R), HER2 kinase were expressed and purified through an insect cell expression system by the Department of Biology, Centaurus B...More data for this Ligand-Target Pair
TargetHigh affinity nerve growth factor receptor [G667C](Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
Affinity DataIC50: 0.210nMAssay Description:TrkAG667C (Kinase domain) kinase was expressed in Sf9 cells by using pIEX-Bac-4, and purified by using affinity chromatography on AKTA Purifier (GE c...More data for this Ligand-Target Pair
TargetHigh affinity nerve growth factor receptor(Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
Affinity DataIC50: 0.210nMAssay Description:A testing platform for TrkAWT kinase activity was established based on Homogeneous Time-Resolved Fluorescence (HTRF) assay, and the activities of the...More data for this Ligand-Target Pair
TargetHigh affinity nerve growth factor receptor [G667C](Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
Affinity DataIC50: 0.220nMAssay Description:TrkAG667C (Kinase domain) kinase was expressed in Sf9 cells by using pIEX-Bac-4, and purified by using affinity chromatography on AKTA Purifier (GE c...More data for this Ligand-Target Pair
TargetHigh affinity nerve growth factor receptor(Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
Affinity DataIC50: 0.230nMAssay Description:A testing platform for TrkAWT kinase activity was established based on Homogeneous Time-Resolved Fluorescence (HTRF) assay, and the activities of the...More data for this Ligand-Target Pair
TargetHigh affinity nerve growth factor receptor(Homo sapiens (Human))
Chia Tai Tianqing Pharmaceutical Group
US Patent
Chia Tai Tianqing Pharmaceutical Group
US Patent
Affinity DataIC50: 0.230nMAssay Description:A testing platform for TrkAWT kinase activity was established based on Homogeneous Time-Resolved Fluorescence (HTRF) assay, and the activities of the...More data for this Ligand-Target Pair