Chemical Structure : USP8 inhibitor W-17
Catalog No.: PC-27996Not For Human Use, Lab Use Only.
USP8 inhibitor W-17 is a potent, selective USP8 inhibitor with IC50 of 108 nM, exhibits no activity against USP7, USP10, and USP14 (IC50>10 uM).
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USP8 inhibitor W-17 is a potent, selective USP8 inhibitor with IC50 of 108 nM, exhibits no activity against USP7, USP10, and USP14 (IC50>10 uM).
W-17 can stabilize USP8 in HCT116 and SW480 cells.
W-17 exhibits minimal inhibitory effects on USP family deubiquitinases, including USP7, USP10, and USP14.
W-17 directly engages USP8 in cells and accelerates PD-L1 proteasomal degradation via enhanced K48-linked polyubiquitination.
W-17 can promote the destabilization of PD-L1 and enhance T-cell mediated tumor cell killing activity.
W-17 (10-20 mg/kg/day) suppresses tumor growth and promotes immune activation in immunocompetent CT26 colorectal cancer model.
| M.Wt | 308.36 | |
| Formula | C13H16N4O3S | |
| Appearance | Solid | |
| Storage |
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| Solubility |
10 mM in DMSO |
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1. Zhiyu Song, et al. Transl Oncol. 2026 Aug 5:72:102956.

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