Ki Summary BindingDB logo
myBDB logout
Reaction Details
Report a problem with these data
TargetRAC-alpha serine/threonine-protein kinase
LigandBDBM50528434
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1904982 (CHEMBL4407340)
IC50 6.4±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:
BDBM50528434
n/a
NameBDBM50528434
Synonyms:CHEMBL4546392
TypeSmall organic molecule
Emp. Form.C26H29Cl4N5O2
Mol. Mass.585.353
SMILESCn1ncc(Cl)c1-c1cc(oc1Cl)C(=O)N[C@@H]1CN[C@H](CCN2CCCC2)C[C@H]1c1ccc(Cl)c(Cl)c1 |r,wU:16.17,19.21,wD:28.32,(7.84,-37.33,;7.52,-38.84,;6.11,-39.46,;6.26,-40.99,;7.77,-41.32,;8.39,-42.72,;8.54,-39.98,;10.08,-39.82,;11.11,-40.97,;12.52,-40.35,;12.36,-38.82,;10.85,-38.49,;10.23,-37.08,;13.85,-41.12,;13.85,-42.66,;15.19,-40.36,;16.52,-41.13,;16.52,-42.66,;17.85,-43.44,;19.18,-42.67,;20.51,-43.45,;21.85,-42.68,;23.18,-43.46,;23.34,-44.98,;24.85,-45.31,;25.62,-43.98,;24.59,-42.83,;19.19,-41.13,;17.86,-40.36,;17.86,-38.83,;16.52,-38.06,;16.52,-36.52,;17.85,-35.75,;17.85,-34.21,;19.19,-36.51,;20.52,-35.73,;19.19,-38.06,)|
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: