| Name | FT709 |
|---|
| Description | FT709 is a potent and selective USP9X inhibitor, an IC50 of 82 nM. USP9X has been linked with centrosome function, chromosome alignment during mitosis, EGF receptor degradation, chemo-sensitization, and circadian rhythms[1]. |
|---|---|
| Related Catalog | |
| References |
| Molecular Formula | C23H22N4O7S |
|---|---|
| Molecular Weight | 498.51 |