Report error Found 53 Enz. Inhib. hit(s) with all data for entry = 50022489
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 1nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 1nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataKi: 3nMAssay Description:Binding affinity to N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells assessed as ...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 5nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 8nMAssay Description:Inhibition of wild-type AKT3 (unknown origin) by HTRF KinEASE assayMore data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 10nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataKi: 30nMAssay Description:Binding affinity to N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells assessed as ...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 38nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 39nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 56nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataKi: 57nMAssay Description:Binding affinity to N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells assessed as ...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataKi: 59nMAssay Description:Binding affinity to N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells assessed as ...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataKi: 71nMAssay Description:Binding affinity to N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells assessed as ...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 119nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 157nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 319nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 381nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 490nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 618nMAssay Description:Inhibition of wild-type AKT3 (unknown origin) by HTRF KinEASE assayMore data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataKi: 755nMAssay Description:Binding affinity to N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells assessed as ...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 813nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 951nMAssay Description:Inhibition of wild-type AKT3 (unknown origin) by HTRF KinEASE assayMore data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 1.14E+3nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 1.24E+3nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataKi: 1.24E+3nMAssay Description:Binding affinity to N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells assessed as ...More data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 1.28E+3nMAssay Description:Inhibition of wild-type AKT3 (unknown origin) by HTRF KinEASE assayMore data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataKi: 1.43E+3nMAssay Description:Binding affinity to N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells assessed as ...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 1.57E+3nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.83E+3nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 3.21E+3nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 5.03E+3nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 5.19E+3nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 5.42E+3nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-alpha serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 5.59E+3nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT1 (2 to 446 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 1.15E+4nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 1.30E+4nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 1.63E+4nMAssay Description:Inhibition of wild-type AKT3 (unknown origin) by HTRF KinEASE assayMore data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 1.77E+4nMAssay Description:Inhibition of wild-type AKT3 (unknown origin) by HTRF KinEASE assayMore data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of wild-type AKT3 (unknown origin) by HTRF KinEASE assayMore data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of wild-type AKT3 (unknown origin) by HTRF KinEASE assayMore data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of wild-type AKT3 (unknown origin) by HTRF KinEASE assayMore data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of wild-type AKT3 (unknown origin) by HTRF KinEASE assayMore data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of wild-type AKT3 (unknown origin) by HTRF KinEASE assayMore data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of wild-type AKT3 (unknown origin) by HTRF KinEASE assayMore data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair
TargetRAC-beta serine/threonine-protein kinase(Human)
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
TU Dortmund University and Drug Discovery Hub Dortmund (DDHD)
Curated by ChEMBL
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of N-terminal His6-tagged TEV protease fused wild-type AKT2 (2 to 447 residues) (unknown origin) expressed in Sf9 cells by HTRF KinEASE as...More data for this Ligand-Target Pair














