ChemicalBook--->CAS DataBase List--->1394076-92-6

1394076-92-6

1394076-92-6 Structure

1394076-92-6 Structure
IdentificationBack Directory
[Name]

5-(6-(3-Methoxyoxetan-3-yl)-4-Morpholinothieno[3,2-d]pyriMidin-2-yl)pyriMidin-2-aMine
[CAS]

1394076-92-6
[Synonyms]

GNE-317
CS-1716
GNE-317;GNE 317;GNE317
5-(6-(3-Methoxyoxetan-3-yl)-4-Morpholinothieno[3,2-d]pyriMidin-2-yl)pyriMidin-2-aMine
5-(6-(3-methoxyoxetan-3-yl)-7-methyl-4-morpholinothieno[3,2-d]pyrimidin-2-yl)pyrimidin-2-amine
5-(6-(3-Methoxyoxetan-3-yl)-4-Morpholinothieno[3,2-d]pyriMidin-2-yl)pyriMidin-2-aMine USP/EP/BP
5-[6-(3-METHOXYOXETAN-3-YL)-7-METHYL-4-MORPHOLIN-4-YLTHIENO[3,2-D]PYRIMIDIN-2-YL]PYRIMIDIN-2-AMINE
2-Pyrimidinamine, 5-[6-(3-methoxy-3-oxetanyl)-7-methyl-4-(4-morpholinyl)thieno[3,2-d]pyrimidin-2-yl]-
[Molecular Formula]

C18H20N6O3S
[MDL Number]

MFCD28900677
[MOL File]

1394076-92-6.mol
[Molecular Weight]

400.455
Chemical PropertiesBack Directory
[storage temp. ]

Keep in dark place,Inert atmosphere,Store in freezer, under -20°C
[solubility ]

Soluble in DMSO
[form ]

A solid
[color ]

Light yellow to khaki
Hazard InformationBack Directory
[Biological Activity]

gne-317 is a potent inhibitor of pi3k [1].phosphatidylinositol-4,5-bisphosphate 3-kinase (pi3k) are a series of enzymes and play an important role in cell growth, proliferation, differentiation, survival, motility and intracellular trafficking.in the gl261 cell line, gne-317 showed cytotoxic activity [2].in mouse brain, gne-317(50 mg/kg) significantly inhibited pakt, p4ebp1 and ps6 by 80%, 84%, and 92% respectively, which were downstream markers of the pi3k/mtor pathway. in u87, gs2 and gbm10 tumor-bearing mice, gne-317 inhibited tumor growth by 90%, 50% and a survival benefit, respectively [1]. in c57b6/j mice inoculated with gl261-gfp-luc cells, the concentrations of gne-317 in the normal brain, tumor core and rim were not significantly different. in tumor-bearing mice, gne-317 significantly reduced the levels of p-aktser473, p-s6ser235/236 and p-4ebp1thr37/46 within the tumor [2]. in u87 and gs2 glioblastoma multiforme (gbm) models, gne-317 was uniformly distributed in the brain. the brain-to-plasma ratios for gne-317 were greater than 1, in agreement with the brain penetration properties of gne-317 [3].
[in vitro]

GNE-317 is not a substrate of P-gp or BCRP transporter in transfected Madin-Darby canine kidney (MDCK) cells. Binding of it to plasma proteins exhibits a free fraction of 14.9 % in mouse plasma, and binding to brain tissues is higher, with a free fraction of 5.4%.It shows cytostasis but no cell death to U87 cells.
[in vivo]

GNE-317 (40 mg/kg, po) markedly inhibits the PI3K pathway in mouse brain, causing 40% to 90% suppression of the pAkt and pS6 signals up to 6-hour postdose. GNE-317 (40 mg/kg, po) ) is ef?cacious in the U87 and GS2 orthotopic models, achieving tumor growth inhibition of 90% and 50%, respectively. In the GBM10 tumor model, GNE-317 (30 mg/kg, po; 40 mg/kg the ?rst 2 weeks) extends the survival of mice from a median of 55.5 to 75 days.
[target]

PI3K

mTOR

[References]

[1]. salphati l, heffron tp, alicke b, et al. targeting the pi3k pathway in the brain--efficacy of a pi3k inhibitor optimized to cross the blood-brain barrier. clin cancer res, 2012, 18(22): 6239-6248.
[2]. becker cm, oberoi rk, mcfarren sj, et al. decreased affinity for efflux transporters increases brain penetrance and molecular targeting of a pi3k/mtor inhibitor in a mouse model of glioblastoma. neuro oncol, 2015, pii: nov081.
[3]. salphati l, shahidi-latham s, quiason c, et al. distribution of the phosphatidylinositol 3-kinase inhibitors pictilisib (gdc-0941) and gne-317 in u87 and gs2 intracranial glioblastoma models-assessment by matrix-assisted laser desorption ionization imaging. drug metab dispos, 2014, 42(7): 1110-1116.
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