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FT709 is a selective USP9X deubiquitinating enzyme inhibitor (IC50=82 nM) that reduces Makorin and ZNF598 levels, impairing ribosomal quality control pathways.

| Pack Size | Price | Availability | Quantity |
|---|---|---|---|
| 1 mg | $287 | In Stock | |
| 5 mg | $928 | In Stock | |
| 10 mg | $1,480 | In Stock | |
| 25 mg | $2,970 | In Stock | |
| 1 mL x 10 mM (in DMSO) | $987 | In Stock |
| Description | FT709 is a selective USP9X deubiquitinating enzyme inhibitor (IC50=82 nM) that reduces Makorin and ZNF598 levels, impairing ribosomal quality control pathways. |
| Targets&IC50 | USP9X:82 nM |
| In vitro | In HCT116 cells, treatment with 10 µM FT709 for 24 hours downregulated the expression levels of ZNF598 (a ubiquitin E3 ligase) and centrosomal protein CEP55 [1]. |
| Synonyms | FT 709 |
| Molecular Weight | 498.51 |
| Formula | C23H22N4O7S |
| Cas No. | 2413991-74-7 |
| Smiles | S(=O)(=O)(N1CC2=C(C1)CN(C([C@@H](O)C3=C4C(OC(C)=N4)=CC=C3)=O)C2)C=5C=C6C(=NC5)OCCO6 |
| Color | White |
| Appearance | Solid |
| Storage | store at low temperature,keep away from moisture | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| Solubility Information | DMSO: 80 mg/mL (160.48 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
Solution Preparation Table | ||||||||||||||||||||||||||||||||||||
DMSO
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