Molecular Formula | C20H31N3O2S2
|
Molar Mass | 409.61 |
Density | 1.162 |
Melting Point | 126-127 °C(Solv: hexane (110-54-3); ethyl acetate (141-78-6)) |
Boling Point | 535.0±43.0 °C(Predicted) |
Solubility | Soluble in DMSO (82 mg/ml), water (< 1 mg/ml), and ethanol (60 mg/ml). |
Appearance | White solid |
Color | White to Off-White |
pKa | 6.03±0.40(Predicted) |
Storage Condition | +2C to +8C |
MDL | MFCD18384970 |
Use | A pleckstrin homology domain inhibitor to Akt and PKB Kinase (PDPK1). |
In vitro study | PH-427 is a platelet leukocyte C kinase substrate homology (PH) domain inhibitor of Akt/pdpk1. 10 M PH-427 acts on PC-3 prostate cancer cells, significantly reduced by p-Ser241-PDPK1 and p-Thr308-Akt, indicating that PHT-427 can inhibit Akt and pdkp1. PHT-427 acts on the plasma membrane and also inhibits Akt and PDKP1 PH domain translocation. PHT-427 induces apoptosis and inhibits AKT phosphorylation (mainly at Ser473 residue and less at Thr308 residue, IC50 is 6.3 μm, which does not affect all AKT protein expression. PHT-427 acts on Panc-1 cells and has an antiproliferative effect with an IC50 of 65 μm. |
In vivo study | PHT-427 acts on BxPC-3 pancreatic cancer, MCF-7 breast cancer and A- 549 NSCL cancer xenografts, with significant anti-tumor activity. PHT-427 at a dose of 125 to 250 mg/kg on BxPC-3, tumor growth was inhibited by 80%. |