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Postion:Product Catalog >Biochemical Engineering>Inhibitors>PI3K / Akt / mTOR>Akt inhibitors>Perifosine (KRX-0401)
Perifosine (KRX-0401)
  • Perifosine (KRX-0401)
  • Perifosine (KRX-0401)

Perifosine (KRX-0401)

Price $2
Package 1kg
Min. Order: 1kg
Supply Ability: 100kg
Update Time: 2019-07-06

Product Details

Product Name: Perifosine (KRX-0401) CAS No.: 157716-52-4
Min. Order: 1kg Purity: 99%
Supply Ability: 100kg Release date: 2019/07/06
Product NUmber: : WM.562
 
 
p
erifosine (KRX-0401) Basic information
Description In vitro In vivo
Product Name: Perifosine (KRX-0401)
Synonyms: Perifosine;(1,1-Dimethylpiperidin-1-ium-4-yl) octadecyl phosphate;4-((Hydroxy(octadecyloxy)phosphinyl)oxy)-1,1-dimethylpiperidinium inner salt;Perifosine,D 21266;4-[[Hydroxy(octadecycloxy)phosphinyl]oxy]-1,1-diMethylpiperidiniuM inner salt;D-21266 octadecyl-(N,N-diMethyl-piperidino-4-yl)-phosphate;NSC 639966;Perifosine(KRX-0401)
CAS: 157716-52-4
MF: C25H52NO4P
MW: 461.663
EINECS: 1592732-453-0
Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals;Antineoplastic;PI3K/Akt/mTOR;Inhibitors;Akt;mTOR;PI3K
Mol File: 157716-52-4.mol
Article illustration
 
Perifosine (KRX-0401) Chemical Properties
Melting point  271-272° (dec)
storage temp.  ?20°C
solubility  H2O: soluble10mg/mL, clear
color  white to beige
InChIKey SZFPYBIJACMNJV-UHFFFAOYSA-N
 
Safety Information
MSDS Information
 
 
Perifosine (KRX-0401) Usage And Synthesis
Description Perifosine (KRX-0401) is a novel Akt inhibitor with IC50 of 4.7 μM in MM.1S cells, targets pleckstrin homology domain of Akt. Phase 3.
In vitro Perifosine develops anti-proliferative properties with IC50 of 0.6-8.9 μM in immortalized keratinocytes (HaCaT), and head and neck squamous carcinoma cells. Perifosine strongly reduces phosphorylation levels of Akt and extracellular signal-regulated kinase (Erk) 1/2, induces cell cycle arrest in G1 and G2, and causes dose-dependent growth inhibition of mouse glial progenitors.  Perifosine (10 μM) completely inhibits the phosphorylation of Akt in MM.1S cells. A recent study demonstrates Perifosine induces cell cycle arrest and apoptosis in human hepatocellular carcinoma cell lines by blockade of Akt phosphorylation.
In vivo Perifosine combining with temozolomide reduces tumor proliferation (a PDGF-driven gliomagenesis) in vivo. The results indicate that Perifosine is an effective drug in gliomas in which Akt and Ras-Erk 1/2 pathways are frequently activated, and may be new candidate for glima treatment in the clinic.  Both oral daily and weekly administration of Perifosine significantly reduce human MM tumor growth and increase survival, compared with control animals treated with PBS vehicle only. Perifosine induces thrombocytosis and leukocytosis and increases myelopoiesis in murine marrow and spleen, whereas it causes apoptosis in myeloma xenografts.
Uses Antineoplastic.
Uses It acts as an Akt inhibitor and a PI3K inhibitor, and is a drug candidate being developed for a variety of cancer indications.
Uses An alkylphospholipid which inhibits Akt activation and the anti-apoptotic MAPK pathway.
Definition ChEBI: A phospholipid consisting of 1,1-dimethylpiperidinium-4-yl hydrogen phosphate in which the hydrogen is replaced by a stearyl (octadecyl) group.
 
   
   
   
   
   
   
   
   
 

Company Profile Introduction

Established in 2014,Career Henan Chemical Co. is a manufacturerspecializing in the sale of fine chemicals. Mainly deals in the sales of: Pharmaceutical intermediates OLED intermediates: Pharmaceutical intermediates; OLED intermediates;

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