BDBM50637405 AZC5363::AZD-5363::AZD5363::Azd 5363::Azd-5363::Capivasertib::Truqap
SMILES NC1(C(=O)N[C@@H](CCO)c2ccc(Cl)cc2)CCN(c2nc[nH]c3nccc2-3)CC1
InChI Key InChIKey=JDUBGYFRJFOXQC-UHFFFAOYSA-N
Data 13 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 13 hits for monomerid = 50637405
Affinity DataIC50: 0.900nMAssay Description:Covalent-allosteric inhibition of full length N-terminal his6-tagged AKT (2 to 446 residues) (unknown origin) expressed in Spodoptera frugiperda Sf9 ...More data for this Ligand-Target Pair
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
Affinity DataIC50: 3nMAssay Description:Inhibition of AKT1 (unknown origin)More data for this Ligand-Target Pair
TargetPlatelet-derived growth factor receptor alpha/beta(Mouse)
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: 3nMAssay Description:Inhibition of AKT phosphorylation in human MDA-MB-231 incubated for 18 hrs by Western blot analysisMore data for this Ligand-Target Pair
Affinity DataIC50: 3nMAssay Description:Inhibition of AKT1 (unknown origin)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)
First People's Hospital of Shangqiu
Curated by ChEMBL
First People's Hospital of Shangqiu
Curated by ChEMBL
Affinity DataIC50: 7nMAssay Description:Inhibition of AKT3 (unknown origin)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: 7nMAssay Description:Inhibition of AKT2 (unknown origin)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: 8nMAssay Description:Inhibition of AKT2 (unknown origin)More data for this Ligand-Target Pair
Affinity DataIC50: 8nMAssay Description:Inhibition of AKT1 (unknown origin)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: 8nMAssay Description:Inhibition of AKT2 (unknown origin)More data for this Ligand-Target Pair
TargetRAC-gamma serine/threonine-protein kinase(Human)
First People's Hospital of Shangqiu
Curated by ChEMBL
First People's Hospital of Shangqiu
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-gamma serine/threonine-protein kinase(Human)
First People's Hospital of Shangqiu
Curated by ChEMBL
First People's Hospital of Shangqiu
Curated by ChEMBL
Affinity DataIC50: 8nMAssay Description:Inhibition of AKT3 (unknown origin)More data for this Ligand-Target Pair
