LY2090314

LY2090314
  • CAS No.:603288-22-8
Other grades of this product :

LY2090314 Basic information
Product Name:LY2090314
Synonyms:LY2090314;7-(2,5-Dihydro-4-imidazo[1,2-a]pyridin-3-yl-2,5-dioxo-1H-pyrrol-3-yl)-9-fluoro-1,2,3,4-tetrahydro-2-(1-piperidinylcarbonyl)pyrrolo[3,2,1-jk][1,4]benzodiazepine;3-(9-fluoro-2-(piperidine-1-carbonyl)-1,2,3,4-tetrahydro-[1,4]diazepino[6,7,1-hi]indol-7-yl)-4-(imidazo[1,2-a]pyridin-3-yl)-1H-pyrrole-2,5-dione;7-(2,5-Dihydro-4-imidazo[1,2-a]pyridin-3-yl-2,5-dioxo-1H-pyrrol-3-yl)-9-fluoro-1,2,3,4-tetrahydro-2-(1-piperidinylcarbonyl)pyrrolo[3,2,1-jk][1,4]benzodiazepine                              LY2090314;LY2090314;LY 2090314;LY-2090314;LY2090314 100MG;CS-843;LY 2090314;LY-2090314
CAS:603288-22-8
MF:C28H25FN6O3
MW:512.53
EINECS:
Product Categories:Inhibitors;Akt;mTOR;PI3K
Mol File:603288-22-8.mol
LY2090314 Chemical Properties
density 1.55±0.1 g/cm3(Predicted)
storage temp. -20°C
solubility insoluble in H2O; ≥91 mg/mL in DMSO; ≥4.27 mg/mL in EtOH with gentle warming and ultrasonic
form powder
pka7.41±0.60(Predicted)
color yellow to orange
CAS DataBase Reference603288-22-8
Safety Information
MSDS Information
LY2090314 Usage And Synthesis
UsesLY 2090314 is a novel glycogen synthase kinase-3α inhibitor for the treatment of acute myeloid leukemia.
Biological Activityly2090314 (ly) is a potent inhibitor of glycogen synthase kinase-3 (gsk-3) which plays an important role in various pathways, such as protein synthesis initiation, cell proliferation/differentiation, and apoptosis.
Biochem/physiol ActionsLY2090314 is a potent and selective ATP-competitive inhibitor of Glycogen synthase kinase-3 (GSK-3) currently in clinical trials for cancer therapy. LY2090314 has IC50 values of 1.5 nM and 0.9 nM for GSK-3α and GSK-3β, respectively.
in vitroly2090314 selectively inhibits the activity of gsk-3 by inhibiting atp binding. ly2090314 was reported to be able to stabilize β-catenin. as monotherapy, ly2090314 aslso showed limited efficacy. in solid tumor cancer cell lines, ly3090314 was found to enhance the efficacy of cisplatin and carboplatin [1].
in vivoeven in mdr1a-, bcrp-, and mrp2-knockout rats, the metabolites of ly2090314 did not appear in systemic circulation, and the urinary excretion was not found to be enhanced, since the hypothesized impaired biliary excretion of metabolites in the absence of these canalicular transporters was not observed. dog metabolite disposition was similar, with the exception of ly2090314 glucuronide. moreover, ly2090314 enhances the efficacy of cisplatin and carboplatin in solid tumor cancer xenografts [1]
IC 501.5 nm (gsk-3α); 0.9 nm (gsk-3β)
references[1] brail lh, et al.  j clin oncol, 2011, 29, abstr 3030.
LY2090314 Preparation Products And Raw materials

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