AZD5363 agillin Smiles: CC1C2=C(SC=1C)N1C(=NN=C1C)[C@H](CC(=O)NCCCCCCCCNC(=O)COC1=CC=CC3=C1C(=O)N(C1CCC(=O)NC1=O)C3=O)N=C2C1C=CC(Cl)=CC=1

Smiles: CC1C2=C(SC=1C)N1C(=NN=C1C)[C@H](CC(=O)NCCCCCCCCNC(=O)COC1=CC=CC3=C1C(=O)N(C1CCC(=O)NC1=O)C3=O)N=C2C1C=CC(Cl)=CC=1

Chemical Name: N-[(1-hexyl-2-hydroxy-1H-indol-3-yl)imino]benzamide

InChi: InChI=1S/C17H27NO2/c1-18(2)13-16(17(19)11-5-4-6-12-17)14-7-9-15(20-3)10-8-14/h7-10

with a gradual return of expression by 48 hours

AZD5363 agillin Smiles: CC1C2=C(SC=1C)N1C(=NN=C1C)[C@H](CC(=O)NCCCCCCCCNC(=O)COC1=CC=CC3=C1C(=O)N(C1CCC(=O)NC1=O)C3=O)N=C2C1C=CC(Cl)=CC=1AZD5363, also known as Capivasertib, is an orally available inhibitor of the serine threonine protein kinase AKT (protein kinase B) with potential antineoplastic activity. AKT inhibitor AZD5363 binds to and inhibits all AKT isoforms. Inhibition of AKT prevents the phosphorylation of AKT substrates that mediate cellular processes, such as cell division, apoptosis, and glucose and fatty acid metabolism. A wide range of solid and hematological