| Cat. No. |
Product Name |
Information |
| PC-45341 |
ML323
USP1 inhibitor
|
ML323 (ML 323) is a potent, selective, reversible inhibitor of the USP1/UAF1 deubiquitinase complex with IC50 of 76 nM. |
| PC-42288 |
ML364
USP2 inhibitor
|
ML364 is a potent, selective and reversible ubiquitin-specific protease USP2 inhibitor with IC50 of 1.1 uM. |
| PC-43555 |
P50429
USP7/USP47 inhibitor
|
P50429 (P 50429) is a potent, selective, covalent deubiquitinase USP7 (EC50=0.42 uM)/USP47 (EC50=1.0 uM) inhibitor with no inhibition for caspase 3, calpain 1, 20S proteasome and a panel of representative USPs. |
| PC-45339 |
HBX 19818
USP7 inhibitor
|
HBX 19818 is a potent, selective USP7 inhibitor with IC50 of 28.1 uM. |
| PC-45856 |
USP8-IN-22d
USP8 inhibitor
|
USP8-IN-22d is a potent, selective ubiquitin-specific protease USP8 inhibitor with IC50 of 0.85 uM. |
| PC-45857 |
USP8-IN-22c
USP8 inhibitor
|
USP8-IN-22c is a potent, selective ubiquitin-specific protease USP8 inhibitor with IC50 of 0.56 uM. |
| PC-45056 |
USP7-IN-1
USP7 inhibitor
|
USP7-IN-1 is a novel selective and reversible inhibitor of USP7 with IC50 of 33 uM. |
| PC-46007 |
SJB3-019A
USP1 inhibitor
|
SJB3-019A is a potent ubiquitin-specific protease USP1 inhibitor with IC50 of 78.1 nM, 5 times more potent than SJB2-043 in promoting ID1 degradation and cytoxicity in K562 cells. |
| PC-26283 |
UC495
OTULIN inhibitor
|
UC495 is a specific small molecule inhibitor of deubiquitinase OTULIN, interacts with the OTULIN deubiquitinase binding pocket. |
| PC-26236 |
USP11 inhibitor 26
USP11 inhibitor
|
USP11 inhibitor 26 (USP11-IN-1) is a selective inhibitor of USP11 with IC50 of 10.9 uM, shows 1.7- and >100-fold selective over USP4 and USP15. |
| PC-26235 |
USP11 inhibitor 7
USP11 inhibitor
|
USP11 inhibitor 7 (USP11-IN-2) is a selective inhibitor of USP11 with IC50 of 2.6 uM, shows >30- and 100-fold selective over USP4 and USP15. |
| PC-26201 |
WWQ-03-012
DESI2 inhibitor
|
WWQ-03-012 is a potent, specific and covalent inhibitor of JAK2‐V617F complex component DESI2 with IC50 of 47.3 nM, selectively degrades mutant JAK2. |
