Molecular Formula | C16H12N2O3 |
Molar Mass | 280.28 |
Melting Point | 249 °C(dec.) |
Solubility | DMSO: soluble |
Appearance | Yellow solid. |
Color | Light yellow to Amber to Dark green |
Storage Condition | Keep in dark place,Sealed in dry,2-8°C |
In vitro study | In DHER-14 cells, AG 494 inhibits Cdk2 activation and EGF-dependent DNA synthesis. AG-494 significantly prevents NF-kB activation in silica-stimulated cells, and also reduces NF-kB activation in H 2 O 2 -treated cells. AG-494 (3-9 μM; 5-7 days) inhibits BMP9-induced ALP activity in a dose-dependent manner. |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
UN IDs | 3439 |
WGK Germany | 3 |
Hazard Class | 6.1 |
Packing Group | III |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 3.542 ml | 17.712 ml | 35.425 ml |
5 mM | 0.708 ml | 3.542 ml | 7.085 ml |
10 mM | 0.354 ml | 1.771 ml | 3.542 ml |
5 mM | 0.071 ml | 0.354 ml | 0.708 ml |
biological activity | AG-494 is an inhibitor of EGFR receptor autophosphorylation with an IC50 of 1.2 μm. It inhibits EGF-dependent cell growth with an IC50 of 6 μm. |
Target | Value |
EGFR (Cell-free assay) | 1.2 μM |