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Target
RAC-alpha serine/threonine-protein kinase
Ligand
BDBM50327795
Substrate
n/a
Meas. Tech.
ChEMBL_664850 (CHEMBL1259574)
IC50
604±n/a nM
Citation
 Blake, JF; Kallan, NC; Xiao, D; Xu, R; Bencsik, JR; Skelton, NJ; Spencer, KL; Mitchell, IS; Woessner, RD; Gloor, SL; Risom, T; Gross, SD; Martinson, M; Morales, TH; Vigers, GP; Brandhuber, BJ Discovery of pyrrolopyrimidine inhibitors of Akt. Bioorg Med Chem Lett 20:5607-12 (2010) [PubMed]  Article 
Target
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:
MSDVAIVKEGWLHKRGEYIKTWRPRYFLLKNDGTFIGYKERPQDVDQREAPLNNFSVAQCQLMKTERPRPNTFIIRCLQWTTVIERTFHVETPEEREEWTTAIQTVADGLKKQEEEEMDFRSGSPSDNSGAEEMEVSLAKPKHRVTMNEFEYLKLLGKGTFGKVILVKEKATGRYYAMKILKKEVIVAKDEVAHTLTENRVLQNSRHPFLTALKYSFQTHDRLCFVMEYANGGELFFHLSRERVFSEDRARFYGAEIVSALDYLHSEKNVVYRDLKLENLMLDKDGHIKITDFGLCKEGIKDGATMKTFCGTPEYLAPEVLEDNDYGRAVDWWGLGVVMYEMMCGRLPFYNQDHEKLFELILMEEIRFPRTLGPEAKSLLSGLLKKDPKQRLGGGSEDAKEIMQHRFFAGIVWQHVYEKKLSPPFKPQVTSETDTRYFDEEFTAQMITITPPDQDDSMECVDSERRPHFPQFSYSASGTA
  
Inhibitor
Name:
BDBM50327795
Synonyms:
(S)-1-(4-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)piperazin-1-yl)-3-amino-2-(4-isopropylbenzyl)propan-1-one | CHEMBL1257513
Type:
Small organic molecule
Emp. Form.:
C23H30N6O
Mol. Mass.:
406.5239
SMILES:
CC(C)c1ccc(C[C@@H](CN)C(=O)N2CCN(CC2)c2ncnc3[nH]ccc23)cc1 |r|
Structure:
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