578.8
C30H58O10
Soluble in DMSO (200 mg/ml). Use anhydrous DMSO for reconstitution.
-20°C
Synonym: 1l-6-hydroxymethyl-chiro-inositol-2-r-2-o-methyl-3-o-octadecylcarbonate
Description:
Potent and selective inhibitor of AKT or Protein Kinase B. AKT inhibitors evolved from adenosine triphosphate (ATP). AKT inhibitors have a potential clinical application in anti-cancer drug development . Weak inhibitor of phosphatidylinositol 3-kinase (PI3-K) (IC= 83 M). Has been shown to inhibit the growth of the following cancer cell lines: HeLa (IC= 2.5 M), HT-29 (IC= 10 M), MCF-7 (IC= 1.2 M), and PC-3 (IC= 2.0 M).
0.1 lbs
Research or further manufacturing use only, not for food or drug use.
