| Name | DT-061 |
|---|
| Description | DT-061 is an orally bioavailable activator of protein phosphatase 2A (PP2A) and could be applied in the therapy of KRAS-mutant and MYC-driven tumorigenesis[1]. |
|---|---|
| Related Catalog | |
| Target |
PP2A[1]. |
| In Vivo | DT-061 (5 mg/kg, oral gavage, 4 weeks) shows single-agent activity in inhibiting H358 or H441 xenograft growth. Additionally, the combination of DT-061 and AZD6244 is more significantly efficient[1]. Animal Model: 6- to 8-week-old male BALB/c nu/nu mice injected with H441 cells (5 × 106)[1]. Dosage: 5 mg/kg. Administration: Oral gavage for 4 weeks. Result: Showed activity in inhibiting tumor growth. |
| References |
| Molecular Formula | C25H23F3N2O5S |
|---|---|
| Molecular Weight | 520.52 |
| Storage condition | 2-8℃ |