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].
Molecular Weight:
498.51
Purity:
99.81
CAS Number:
[2413991-74-7]
Formula:
C23H22N4O7S
Target:
Deubiquitinase
Application Notes:
Reference compound
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