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Daraxonrasib (RAS-IN-2; RMC-6236) is a potent pan-KRAS inhibitor targeting activation-state KRAS for cancer-related studies.
| Cell Experiment | |
|---|---|
| Cell lines | FOB 1.19, MG63, HOS, HOS-MNNG, HOS-143B, Saos2, and U2OS cells |
| Preparation method | Cells were seeded in 96-well plates at a density of 1.0 × 104 cells per well for 24-hour treatment. The cells were treated with DMSO or various doses of daraxonrasib (3, 5, 6, 10, 15, 30, 60, or 100 nM). After treatment, the cells were incubated with MTT solution (5 mg/ml) for 1 h. The media was then replaced with DMSO. Colorimetric changes were measured at 570 nm using a microplate reader. |
| Concentrations | 3, 5, 6, 10, 15, 30, 60, or 100 nM |
| Incubation time | 24 h |
| Animal Experiment | |
|---|---|
| Animal models | WT C57BL/6 mice, Batf3−/− mice, and OT-I mice |
| Formulation | 10% DMSO, 20% polyethylene glycol 400, 10% Kolliphor HS15, and 60% water |
| Dosages | 25 mg/kg/day |
| Administration | Oral gavage |
| Molecular Weight | 811.05 |
| Formula | C44H58N8O5S |
| CAS Number | 2765081-21-6 |
| Form | Solid |
| Solubility (25°C) | DMSO 90 mg/mL |
| Storage | Powder -20°C |
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