Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetRAC-alpha serine/threonine-protein kinase
LigandBDBM50528479
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1904982 (CHEMBL4407340)
IC50 8.8±n/a nM
Citation Dong, XZhan, WZhao, MChe, JDai, XWu, YXu, LZhou, YZhao, YTian, TCheng, GJin, ZLi, JShao, YHe, QYang, BWeng, QHu, Y Discovery of 3,4,6-Trisubstituted Piperidine Derivatives as Orally Active, Low hERG Blocking Akt Inhibitors via Conformational Restriction and Structure-Based Design. J Med Chem62:7264-7288 (2019) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
RAC-alpha serine/threonine-protein kinase
Name:RAC-alpha serine/threonine-protein kinase
Synonyms:AKT phosphorylation (p-AKT) | AKT1 | AKT1/PPP1CA | AKT1_HUMAN | C-AKT | PKB | PKB alpha | Protein kinase Akt-1 | Protein kinase B | Protein kinase B (AKT1) | Protein kinase B (Akt 1) | Protein kinase B (Akt) | Protein kinase B alpha | Protein kinase B alpha (AKT1) | Proto-oncogene Akt (Akt1) | Proto-oncogene c-Akt (AKT) | Proto-oncogene c-Akt (AKT1) | RAC | RAC-PK-alpha | RAC-alpha serine/threonine-protein kinase (AKT) | RAC-alpha serine/threonine-protein kinase (AKT1) | RAC-alpha serine/threonine-protein kinase (pAKT)
Type:Enzyme
Mol. Mass.:55681.25
Organism:Homo sapiens (Human)
Description:P31749
Residue:480
Sequence:
MSDVAIVKEGWLHKRGEYIKTWRPRYFLLKNDGTFIGYKERPQDVDQREAPLNNFSVAQC
QLMKTERPRPNTFIIRCLQWTTVIERTFHVETPEEREEWTTAIQTVADGLKKQEEEEMDF
RSGSPSDNSGAEEMEVSLAKPKHRVTMNEFEYLKLLGKGTFGKVILVKEKATGRYYAMKI
LKKEVIVAKDEVAHTLTENRVLQNSRHPFLTALKYSFQTHDRLCFVMEYANGGELFFHLS
RERVFSEDRARFYGAEIVSALDYLHSEKNVVYRDLKLENLMLDKDGHIKITDFGLCKEGI
KDGATMKTFCGTPEYLAPEVLEDNDYGRAVDWWGLGVVMYEMMCGRLPFYNQDHEKLFEL
ILMEEIRFPRTLGPEAKSLLSGLLKKDPKQRLGGGSEDAKEIMQHRFFAGIVWQHVYEKK
LSPPFKPQVTSETDTRYFDEEFTAQMITITPPDQDDSMECVDSERRPHFPQFSYSASGTA
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50528479
n/a
NameBDBM50528479
Synonyms:CHEMBL4450403
TypeSmall organic molecule
Emp. Form.C26H29Cl4N5O3
Mol. Mass.601.352
SMILESCn1ncc(Cl)c1-c1cc(oc1Cl)C(=O)N[C@@H]1CN[C@H](CCN2CCOCC2)C[C@H]1c1ccc(Cl)c(Cl)c1 |r,wU:16.17,19.21,wD:29.33,(61.2,-37.04,;60.88,-38.54,;59.47,-39.16,;59.63,-40.7,;61.13,-41.02,;61.76,-42.43,;61.91,-39.69,;63.44,-39.53,;64.47,-40.68,;65.88,-40.05,;65.72,-38.52,;64.22,-38.2,;63.59,-36.79,;67.22,-40.83,;67.21,-42.37,;68.55,-40.06,;69.88,-40.83,;69.88,-42.37,;71.21,-43.14,;72.55,-42.38,;73.88,-43.15,;75.21,-42.39,;76.54,-43.16,;76.53,-44.7,;77.85,-45.47,;79.19,-44.72,;79.2,-43.17,;77.87,-42.39,;72.55,-40.83,;71.22,-40.07,;71.22,-38.54,;69.89,-37.77,;69.89,-36.22,;71.22,-35.45,;71.21,-33.91,;72.55,-36.21,;73.88,-35.44,;72.56,-37.76,)|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: