product name GSK2292767
Description: GSK2292767 is a potent and selective PI3Kδ inhibitor. GSK2292767 was found to be greater than 100-fold selective against a panel of in-house kinases and in the Millipore panel. Moreover, GSK2292767 could inhibit both IFNγ and IL-2 production in a concentration-dependent manner in a human lung parenchyma assay, with pIC50s of 8.7 and 8.5, respectively. In a rat PK study, the in vivo clearance for GSK2292767 was significantly higher than that for its analog GSK2269557. The oral bioavailability was also low (F < 2%), which was consistent with the data observed for GSK2269557.
References: J Med Chem. 2015 Sep 24;58(18):7381-99.
512.58
Formula
C24H28N6O5S
CAS No.
1254036-66-2
Storage
-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)
DMSO: 100 mg/mL (195.1 mM)
Water: <1 mg/mL
Ethanol: <1 mg/mL
Solubility (In vivo)
Synonyms
other peoduct :
| In Vitro |
In vitro activity: GSK2292767 was found to be greater than 100-fold selective against a panel of in-house kinases and in the Millipore panel. Moreover, GSK2292767 could inhibit both IFNγ and IL-2 production in a concentration-dependent manner in a human lung parenchyma assay, with pIC50s of 8.7 and 8.5, respectively. Kinase Assay: Cell Assay: |
|---|---|
| In Vivo | In a rat PK study, the in vivo clearance for GSK2292767 was significantly higher than that for its analog GSK2269557. The oral bioavailability was also low (F < 2%), which was consistent with the data observed for GSK2269557. In a rabbit cardiac ventricular wedge assay, no effect on QT interval, Tp e, or QRS and no significant risk of TdP arrhythmias was observed for GSK2292767 over the concentration range tested, thus indicating GSK2292767 could successfully mitigate the risk associated with GSK2269557. Moreover, GSK2292767 was found to protect against eosinophil recruitment with an ED50 of 35 μg/kg in the brown Norway rat acute OVA model, which was similar to GSK2269557. |
| Animal model | |
| Formulation & Dosage | |
| References | J Med Chem. 2015 Sep 24;58(18):7381-99. |
