Molecular Formula | C15H8Br2INO2 |
Molar Mass | 520.94 |
Density | 2.248±0.06 g/cm3(Predicted) |
Boling Point | 561.4±50.0 °C(Predicted) |
Solubility | DMSO: soluble |
Appearance | solid |
Color | yellow to orange-brown |
pKa | 5.86±0.25(Predicted) |
Storage Condition | room temp |
Stability | Stable for 2 years from date of purchase as supplied. Solutions in DMSO may be stored at -20°C for up to 1 month. |
MDL | MFCD03453076 |
Use | GW5074 |
In vitro study | GW5074 is a potent, specific c-Raf inhibitor with an IC50 of 9 nM and has no inhibitory activity against MEK6, MKK7, p38 MAP kinase and cdks in vitro. However, treatment of the neuronal medium with GW5074 accumulated c-Raf and B- Raf of the activation modification. GW5074 inhibits LK-induced apoptosis in cerebellar granule neurons in a MEK-ERK independent manner. GW5074 delays down-regulation of Akt activity, but inhibits apoptosis through an Akt-independent mechanism. GW5074 affects Ras, NF-kappa B and c-jun. GW5074 acts on granulosa cells and other neuronal types to inhibit cell death caused by neurotoxins. GW5074 is a potent, specific c-Raf inhibitor with an IC50 of 9 nM and no inhibitory activity against MEK6, MKK7, p38 MAP kinase and cdks in vitro. However, treatment of the neuronal medium with GW5074 accumulated c-Raf and B- Raf of the activation modification. GW5074 inhibits LK-induced apoptosis in cerebellar granule neurons in a MEK-ERK independent manner. GW5074 delays down-regulation of Akt activity, but inhibits apoptosis through an Akt-independent mechanism. GW5074 affects Ras, NF-kappa B and c-jun. GW5074 acts on granulosa cells and other neuronal types to inhibit cell death caused by neurotoxins. |
In vivo study | GW5074 protects an in vivo experimental model of Huntington's disease. Treatment of mice with GW5074(5 mg/kg) completely inhibited 3-NP-induced bilateral striatal lesions. GW5074 acts on CHO cells stably expressing human opioid receptors, completely abrogating chronic morphine-mediated AC hyperactivation I. GW5074 treated mice inhibited lateral flow smoke induced airway hyperresponsiveness. GW5074 protects an in vivo experimental model of Huntington's disease. Treatment of mice with GW5074(5 mg/kg) completely inhibited 3-NP-induced bilateral striatal lesions. GW5074 acts on CHO cells stably expressing human opioid receptors, completely abrogating chronic morphine-mediated AC hyperactivation I. GW5074 treated mice inhibited lateral flow smoke induced airway hyperresponsiveness. |
WGK Germany | 3 |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 1.92 ml | 9.598 ml | 19.196 ml |
5 mM | 0.384 ml | 1.92 ml | 3.839 ml |
10 mM | 0.192 ml | 0.96 ml | 1.92 ml |
5 mM | 0.038 ml | 0.192 ml | 0.384 ml |