Fig. 1 · Structure
Documents & Downloads
FT709
USP9X Inhibitor
FT709 is a potent and selective inhibitor of USP9X, demonstrating an IC50 value of 82 nM. This compound is implicated in various biological processes, including centrosome function, chromosome alignment during mitosis, and degradation of the EGF receptor. Additionally, FT709 has potential applications in enhancing chemosensitization and studying circadian rhythms, making it a valuable tool for cancer research and cellular biology studies.
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Specifications
| Manufacturer | Adooq Bioscience |
|---|---|
| Actions | Inhibitor |
| CAS Number | 2413991-74-7 |
| Applications | USP9X Inhibitor |
| Formula | C23H22N4O7S |
| Molecular Weight | 498.51 |
| SMILES | O=S(C1=CN=C2C(OCCO2)=C1)(N3CC(CN(C([C@@H](O)C4=CC=CC5=C4N=C(C)O5)=O)C6)=C6C3)=O |
Storage & Solubility
In Vitro Solubility
Reported Solubility
No reported solubility data are available for this product.
Preparing Stock Solutions
| Concentration | |
|---|---|
Values use four significant digits. Prepare to the final solution volume; this is not the volume of solvent to add.
Stock preparation is unavailable for this product molecular weight.
Calculated stock concentrations do not establish solvent solubility. Refer to the reported solubility data for experimental guidance.
Storage
Store powder at -20°C, keep desiccated.
In powder form, the chemical is stable for 36 months.
In solution, store at -20°C and use within 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.