GSK-3BETA INHIBITOR XII
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
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
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.
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