TWS119 structure
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Common Name | TWS119 | ||
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CAS Number | 601514-19-6 | Molecular Weight | 318.329 | |
Density | 1.4±0.1 g/cm3 | Boiling Point | 646.0±55.0 °C at 760 mmHg | |
Molecular Formula | C18H14N4O2 | Melting Point | N/A | |
MSDS | Chinese USA | Flash Point | 344.5±31.5 °C | |
Symbol |
GHS07 |
Signal Word | Warning |
Use of TWS119TWS119 is a specific inhibitor of GSK-3β, with an IC50 of 30 nM, and activates the wnt/β-catenin pathway. |
Name | 3-[[6-(3-aminophenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]oxy]phenol |
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Synonym | More Synonyms |
Description | TWS119 is a specific inhibitor of GSK-3β, with an IC50 of 30 nM, and activates the wnt/β-catenin pathway. |
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Related Catalog | |
Target |
GSK-3β:30 nM (IC50) |
In Vitro | TWS119 induces neuronal differentiation in P19 EC cells and primary mouse ESCs. TWS119 binds to GSK-3β with KD of 126 nM, and modulates the activity of the complex, triggering downstream transcriptional events that lead the neuronal induction[1]. TWS119 (< 4 μM) significantly enhances the proliferation and survival of γδT cells via activation of the mammalian target of rapamycin (mTOR) pathway, upregulation of the expression of anti-apoptotic protein Bcl-2 and inhibition of cleaved caspase-3. TWS119 (0-8 μM) induces the generation of CD62L+γδT or CCR5+γδT cell phenotypes. TWS119 (0.5, 1.0 and 2 μM) increases the expression level of granzyme B in a dose-dependent manner. TWS119 also enhances the cytolytic activity of γδT cells against tumour cells in vitro[3]. |
In Vivo | TWS119 (30 mg/kg, i.p.) improves the neurologic function and decreases neurologic deficit dcore in rtPA-treated MCAO rats. TWS119 effectively relieves cerebral edema, and reduces cerebral infarction in rats treated with rtPA. TWS119 also effectively decreases blood-brain barrier permeability in rtPA-Treated MCAO Rats and attenuates rtPA-induced hemorrhage in ischemic brain tissue. Futhermore, TWS119 activates the Wnt/β-Catenin signaling pathway and increases the expression of Claudin-3 and ZO-1[2]. |
Cell Assay | PBMCs are cultured with pamidronate disodium for 8 days and then cells are labelled with or without 1.5 μM carboxyfluorescein succinimidyl ester (CFSE) and CFSE-labelled cells are then seeded in 6-well plates (2.5 × 106 cells/well) followed by treatment with various concentrations of TWS119 for 72 h. The total number of cultured cells is evaluated using an automated cell counter and the γδT cell proliferation is examined by flow cytometry[3]. |
Animal Admin | All rats are randomly divided into four groups as follows: Sham group-rats undego the same surgical procedure, but the filament is not inserted and they receive 1 mL of dimethyl sulfoxide (1 % DMSO in saline); Vehicle group-rats undergo MCAO and receive 1 mL of DMSO; rtPA group-rats underwent MCAO and receive rtPA (10 mg/kg, Actilyse®) at 4 h after MCAO; and rtPA+TWS119 group-rats undergo MCAO and receive intraperitoneal TWS119 (30 mg/kg, dissolved in 1 mL 1 % DMSO) immediately after rtPA injection at 4 h after MCAO[2]. |
References |
Density | 1.4±0.1 g/cm3 |
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Boiling Point | 646.0±55.0 °C at 760 mmHg |
Molecular Formula | C18H14N4O2 |
Molecular Weight | 318.329 |
Flash Point | 344.5±31.5 °C |
Exact Mass | 318.111664 |
PSA | 97.05000 |
LogP | 3.54 |
Appearance of Characters | light yellow solid |
Vapour Pressure | 0.0±2.0 mmHg at 25°C |
Index of Refraction | 1.753 |
Storage condition | Desiccate at +4°C |
Symbol |
GHS07 |
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Signal Word | Warning |
Hazard Statements | H302-H319 |
Precautionary Statements | P280-P301 + P312 + P330-P305 + P351 + P338-P337 + P313 |
RIDADR | NONH for all modes of transport |
~80% TWS119 CAS#:601514-19-6 |
Literature: Mayasundari, Anand; Fujii, Naoaki Tetrahedron Letters, 2010 , vol. 51, # 27 p. 3597 - 3598 |
~54% TWS119 CAS#:601514-19-6 |
Literature: Mayasundari, Anand; Fujii, Naoaki Tetrahedron Letters, 2010 , vol. 51, # 27 p. 3597 - 3598 |
3-{[6-(3-Aminophenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]oxy}phenol |
GSK-3beta Inhibitor XII |
TWS 119 |
Neurogenesis Inducer |
Phenol, 3-[[6-(3-aminophenyl)-7H-pyrrolo[2,3-d]pyrimidin-4-yl]oxy]- |
TWS119 |