BDBM50405635 CHEMBL5267341
SMILES Cc1nc(-c2ccc(CN3CCC(CC3)n3c4cc(NC(=O)C=C)ccc4[nH]c3=O)cc2)c([nH]c1=O)-c1ccccc1
InChI Key InChIKey=VDTRPZUYLDIREH-UHFFFAOYSA-N
Data 1 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 5 hits for monomerid = 50405635
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: 38nMAssay Description:Inhibition of AKT1 (unknown origin)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: 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-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
