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GSK2292767 is a potent and selective inhibitor of PI3Kδ.

| Pack Size | Price | USA Warehouse | Global Warehouse | Quantity |
|---|---|---|---|---|
| 1 mg | $159 | 35 days | 35 days | |
| 5 mg | $716 | 35 days | 35 days | |
| 10 mg | $1,280 | 35 days | 35 days | |
| 25 mg | $2,880 | 35 days | 35 days |
| Description | GSK2292767 is a potent and selective inhibitor of PI3Kδ. |
| Targets&IC50 | PI3Kδ:10.1 (pIC50) |
| In vitro | BI-847325 shows growth-inhibitory effects on BRAF-mutant and vemurafenib-resistant melanoma cells with IC50 ranging from 0.3 nM to 2 μM, and prevents colony formation in six BRAF-mutant melanoma cell lines. BI-847325 also induces apoptosis by reducing Mcl-1 expression. [1] |
| In vivo | GSK2292767 is highly selective for PI3Kδ over the closely related isoforms and is active in a disease relevant brown Norway rat acute OVA model of Th2-driven lung inflammation[1]. |
| Molecular Weight | 512.58 |
| Formula | C24H28N6O5S |
| Cas No. | 1254036-66-2 |
| Smiles | C(C=1OC(C2=C3C(=CC(=C2)C=4C=C(NS(C)(=O)=O)C(OC)=NC4)NN=C3)=NC1)N5C[C@H](C)O[C@H](C)C5 |
| Relative Density. | 1.360 g/cm3 (Predicted) |
| Storage | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 93 mg/mL (181.44 mM), Sonication is recommended. Ethanol: <1 mg/mL H2O: <1 mg/mL | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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Dissolve 2 mg of the compound in 100 μL DMSO
to obtain a stock solution at a concentration of 20 mg/mL . If the required concentration exceeds the compound's known solubility, please contact us for technical support before proceeding.
1) Add 100 μL of the DMSO
stock solution to 400 μL PEG300
and mix thoroughly until the solution becomes clear.
2) Add 50 μL Tween 80 and mix well until fully clarified.
3) Add 450 μL Saline,PBS or ddH2O
and mix thoroughly until a homogeneous solution is obtained.
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