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PHT-427

Cat. No. M1900

All AbMole products are for research use only, cannot be used for human consumption.

PHT-427 Structure
Size Price Availability Quantity
10mg USD 50 In stock
25mg USD 110 In stock
50mg USD 180 In stock
100mg USD 305 In stock
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Quality Control & Documentation
Biological Activity

PHT-427 is a novel small-molecule inhibitor of PDPK1/Akt signaling with significant antitumor activity and minimal toxicity in vivo. The phosphatidylinositol 3-kinase/AKT signaling pathway plays a critical role in activating survival and antiapoptotic pathways within cancer cells. PHT-427 binds selectively to the PH domain of AKT, causing apoptosis at low micromolar concentrations. And it also binds to the PH domain of PDPK1. PHT-427 inhibited Akt and PDPK1 signaling and their downstream targets in sensitive but not resistant cells and tumor xenografts. PHT-427 induces apoptosis (IC50 = 6.3 μM), mainly on Akt Ser473 residue and less strongly on the Akt Thr308 residue without affecting total Akt protein expression. PHT-427 also shows antiproliferation in Panc-1 cells (IC50 = 65 μM).

Protocol (for reference only)
Cell Experiment
Cell lines Human MiaPaCa-2, BxPC-3, and Panc-1 pancreatic cancer cells
Preparation method Cell cytotoxicity assay
Cell growth inhibition was determined using a micro-cytoxicity assay. Cells were plated in 96-well micro-cytoxicity at 5,000–10,000 cells per well (depending on cell doubling time) and grown for 7 days. Compounds dissolved in DMSO were added directly to the media, at various concentrations ranging from 1 to 50 μM. The endpoint was spectrophotometric determination of the protein content of each well using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide. A concentration-response relationship at two or more concentration levels was used to obtain an IC50 for the compound.
Concentrations 1~50 μM
Incubation time 48 h
Animal Experiment
Animal models BxPC-3, Panc-1, MiaPaCa-2, PC-3, SKOV-3, A-549 or MCF-7 cells tumour model in female scid mice
Formulation 40 to 50 mg/ml in sesame seed oil
Dosages 200 mg/kg twice daily for 10 days
Administration oral
Chemical Information
Molecular Weight 409.61
Formula C20H31N3O2S2
CAS Number 1191951-57-1
Solubility (25°C) DMSO 80 mg/mL
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Meuillet EJ, et al. Mol Cancer Ther. Molecular pharmacology and antitumor activity of PHT-427, a novel Akt/phosphatidylinositide-dependent protein kinase 1 pleckstrin homology domain inhibitor.

[2] Moses SA, et al. Cancer Res. In vitro and in vivo activity of novel small-molecule inhibitors targeting the pleckstrin homology domain of protein kinase B/AKT.

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Keywords: PHT-427 supplier, Akt, inhibitors, activators

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