ChemicalBook > CAS DataBase List > DT-061
DT-061
- Product Name
- DT-061
- CAS No.
- 1809427-19-7
- Chemical Name
- DT-061
- Synonyms
- DT-061(SMAP);DT061,DT 061;N-((1R,2R,3S)-2-Hydroxy-3-(10H-phenoxazin-10-yl)cyclohexyl)-4-(trifluoromethoxy)benzenesulfonamide;Benzenesulfonamide, N-[(1R,2R,3S)-2-hydroxy-3-(10H-phenoxazin-10-yl)cyclohexyl]-4-(trifluoromethoxy)-
- CBNumber
- CB25419728
- Molecular Formula
- C25H23F3N2O5S
- Formula Weight
- 520.52
- MOL File
- 1809427-19-7.mol
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DT-061 Property
- Boiling point:
- 625.5±65.0 °C(Predicted)
- Density
- 1.51±0.1 g/cm3(Predicted)
- storage temp.
- Store at -20°C
- solubility
- DMSO : 125 mg/mL (240.14 mM);Water : < 0.1 mg/mL (insoluble)
- form
- Solid
- pka
- 10.48±0.60(Predicted)
- color
- Off-white to light yellow
- SMILES
- O[C@H]1[C@@H](CCC[C@@H]1N2C3=C(OC4=C2C=CC=C4)C=CC=C3)NS(C5=CC=C(C=C5)OC(F)(F)F)(=O)=O
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N-Bromosuccinimide Price
Sigma-Aldrich
- Product number
- SML4143
- Product name
- DT-061
- Purity
- ≥98% (HPLC)
- Packaging
- 1 unit
- Price
- $94.05
- Updated
- 2025/07/31
ChemScene
- Product number
- CS-0069645
- Product name
- DT-061
- Purity
- 99.97%
- Packaging
- 5mg
- Price
- $350
- Updated
- 2021/12/16
ChemScene
- Product number
- CS-0069645
- Product name
- DT-061
- Purity
- 99.97%
- Packaging
- 10mg
- Price
- $550
- Updated
- 2021/12/16
ChemScene
- Product number
- CS-0069645
- Product name
- DT-061
- Purity
- 99.97%
- Packaging
- 50mg
- Price
- $1950
- Updated
- 2021/12/16
ChemScene
- Product number
- CS-0069645
- Product name
- DT-061
- Purity
- 99.97%
- Packaging
- 100mg
- Price
- $2950
- Updated
- 2021/12/16
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DT-061 Chemical Properties,Usage,Production
Uses
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].
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
[1] Kauko O, et al. PP2A inhibition is a druggable MEK inhibitor resistance mechanism in KRAS-mutant lung cancer cells. Sci Transl Med. 2018 Jul 18;10(450). pii: eaaq1093. DOI:10.1126/scitranslmed.aaq1093
DT-061 Preparation Products And Raw materials
Raw materials
Preparation Products
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