Molecular Formula | C18H12N6OS |
Molar Mass | 360.39 |
Density | 1.53±0.1 g/cm3(Predicted) |
Boling Point | 627.0±65.0 °C(Predicted) |
Solubility | DMSO : 83.3 mg/mL (231.14 mM; Need ultrasonic) |
Appearance | Tan solid |
Color | white to beige |
pKa | 0.85±0.30(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 3 months. |
In vitro study | VAS2870 is effective to suppress PDGF-BB-dependent activation of NADPH oxidase and subsequent production of intracellular ROS. Furthermore, VAS2870 suppresses PDGF-BB-dependent chemotaxis, but not DNA synthesis. Preincubation with VAS2870 (10 and 20 μM) completely abolishes PDGF-mediated NADPH oxidase activation and ROS production. Preincubation with VAS2870 (0.1-20 μM) does not affect PDGF-induced cell cycle progression. However, it abolishes PDGF-dependent chemotaxis of VSMC in a concentration-dependent manner (100% inhibition at 10 μM). VAS2870 inhibits dose-dependently autocrine increase of cell number in FaO rat hepatoma cells, and almost completely blocked ROS production and thymidine incorporation when used at 25 mM. VAS2870 blocks serum-dependent cell growth of FaO rat hepatoma cells. VAS2870 inhibits proliferation of different human hepatocellular carcinoma (HCC) cell lines. VAS2870 pretreatment enhances TGF-b-mediated apoptosis of FaO rat hepatoma cells. |
Hazard Symbols | Xn - Harmful |
Risk Codes | 22 - Harmful if swallowed |
WGK Germany | 3 |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 2.775 ml | 13.874 ml | 27.748 ml |
5 mM | 0.555 ml | 2.775 ml | 5.55 ml |
10 mM | 0.277 ml | 1.387 ml | 2.775 ml |
5 mM | 0.055 ml | 0.277 ml | 0.555 ml |
introduction | VAS-2870 (722456-31-7) is a NAD(P)H oxidase (Nox) inhibitor. It can inhibit PMA-induced oxidative reaction in HL-60 cells (IC50=2 μM) and enhance TGF-β-induced apoptosis of liver tumor cells. |
biological activity | VAS2870 is a pan-NADPH oxidase(NOX) inhibitor. |
target | TargetValue NADPH oxidase () |
Target | Value |
in vitro study | VAS2870 is effective to suppress PDGF-BB-dependent activation of NADPH oxidase and subsequent production of intracellular ROS. Furthermore, VAS2870 suppresses PDGF-BB-dependent chemotaxis, but not DNA synthesis. Preincubation with VAS2870 (10 and 20 μM) completely abolishes PDGF-mediated NADPH oxidase activation and ROS production. Preincubation with VAS2870 (0.1-20 μM) does not affect PDGF-induced cell progression. However, it abolishes PDGF-dependent chemotaxis of VSMC in a concentration-dependent manner (100% inhibition at 10 μM). VAS2870 inhibits dose-dependently autocrine increase of cell number in FaO rat hepatoma cells, and almost completely blocked ROS production and thymidine incorporation when used at 25 mM. VAS2870 blocks series-dependent cell growth of FaO rat hepatoma cells. VAS2870 inhibits proliferation of different human hepatocellular carcinoma (HCC) cell lines. VAS2870 pretreatment enhances TGF-b-mediated apoptosis of FaO rat hepatoma cells. |