Molecular Formula | C19H19N3O2 |
Molar Mass | 321.37 |
Solubility | DMSO: soluble10mg/mL, clear |
Appearance | powder |
Color | white to beige |
Storage Condition | Inert atmosphere,Store in freezer, under -20°C |
Stability | Stable for 1 year from date of purchase as supplied. Solutions in DMSO or ethanol may be stored at -20° for up to 3 months. |
In vitro study | ME0328 is soluble, cell permeable, and metabolically stable in human liver microsomes and rat hepatocytes. In A549 and MRC5 cells, ME0328 (10 μm) significantly delayed the γH2AX site by affecting ARTD3 without significant toxicity. |
Hazard Symbols | Xn - Harmful |
Risk Codes | R22 - Harmful if swallowed R43 - May cause sensitization by skin contact |
Safety Description | 36/37 - Wear suitable protective clothing and gloves. |
WGK Germany | 3 |
1mg | 5mg | 10mg | |
---|---|---|---|
1 mM | 3.112 ml | 15.558 ml | 31.117 ml |
5 mM | 0.622 ml | 3.112 ml | 6.223 ml |
10 mM | 0.311 ml | 1.556 ml | 3.112 ml |
5 mM | 0.062 ml | 0.311 ml | 0.622 ml |
biological activity | ME0328 is a potent selective PARP inhibitor with an IC50 of 0.89 μM, and its selectivity to PARP3 is about seven times higher than that to PARP1. |
In vitro studies | ME0328 is soluble, permeable cells, and metabolically stable in human liver microsomes and rat liver cells. In A549 and MRC5 cells, ME0328 (10 μM) significantly delayed the γH2AX site by affecting ARTD3 without significant toxicity. |
target | ARTD3/PARP3 0.89 μ m (IC 50 ) ARTD1/PARP1 6.3 μ m (IC 50 ) ARTD2/PARP2 10.8 μ m (IC 50 ) ARTD6/TNKS2 34.3 μ m (IC 50 ) ARTD5/TNKS1 47.3 μ m (IC 50 ) ARTD10/PARP10 71.3 μ m (IC 50 ) |