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GSK-3BETA INHIBITOR XII

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GSK-3BETA INHIBITOR XII Basic information

Product Name:
GSK-3BETA INHIBITOR XII
Synonyms:
  • TWS119
  • GSK-3BETA INHIBITOR XII
  • 3-[6-(3-AMINO-PHENYL)-7H-PYRROLO[2,3-D]PYRIMIDIN-4-YLOXY]-PHENOL
  • CS-1924
  • TWS-119; TWS 119
  • CS-445
  • OTAVA-BB 7070707013
  • 3-[[6-(3-Aminophenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]oxyphenolditrifluoroacetate
CAS:
601514-19-6
MF:
C18H14N4O2
MW:
318.33
Product Categories:
  • Akt
  • mTOR
  • Inhibitors
  • PI3K
Mol File:
601514-19-6.mol
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GSK-3BETA INHIBITOR XII Chemical Properties

Melting point:
249 °C
Density 
1.42
storage temp. 
2-8°C
solubility 
insoluble in H2O; insoluble in EtOH; ≥15.9 mg/mL in DMSO
pka
8.99±0.10(Predicted)
form 
powder
color 
white to beige
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GSK-3BETA INHIBITOR XII Usage And Synthesis

Uses

TWS119 has been used as glycogen synthase kinase-3β (GSK-3β) GSK3β inhibitor.

Uses

Acts as an ARMS-selective inihibitor, through GSK3 (Glucose Synthase Kinase 3) inhibition.

Definition

ChEBI: 3-[[6-(3-aminophenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]oxy]phenol is a member of pyrroles.

General Description

A cell-permeable and potent inhibitor of GSK-3β (IC50 = 30 nM). Binds to GSK-3β with high-affinity (Kd = 126 nM), leading to an increase in the level of β-catenin, a downstream substrate of GSK-3β in the Wnt signaling pathway. Shown to selectively induce neuronal differentiation in both pluripotent murine embryonal carcinoma cells (P19; 30-40% at 1 μM) and embryonic stem cells (D3; 50-60% at 400 nM).

Biological Activity

Inhibitor of glycogen synthase kinase-3 β (IC 50 = 30 nM). Induces neuronal differentiation in pluripotent murine embryonal carcinoma cells and embryonic stem cells (ESCs).

Biochem/physiol Actions

TWS119 favors the γδT cells survival and proliferation by activating the mammalian target of rapamycin (mTOR) pathway. It also promotes the expression of T-cell factor 1 (TCF1) and modulates cytokine production.

target

GSK-3β

storage

Store at +4°C

References

[1] ding s, wu t y h, brinker a, et al. synthetic small molecules that control stem cell fate. proceedings of the national academy of sciences, 2003, 100(13): 7632-7637.
[2] wu t y h, ding s. applying chemical tools to the discovery of novel regenerative medicine. drug discovery today: technologies, 2006, 3(3): 255-260.

GSK-3BETA INHIBITOR XIISupplier

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