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Request The Product List ofDeubiquitinase (DUB) Deubiquitinase (DUB)

Cat. No. Product Name Information
PC-72219

IMP-1710

UCHL1 inhibitor

IMP-1710 (IMP1710) is a potent, selective, covalent UCHL1 inhibitor with IC50 of 38 nM.
PC-38192

USP7-866

USP7 inhibitor

USP7-866 is a novel potent selective inhibitor of USP7 with IC50 of 0.18 nM.
PC-38191

USP7-797

USP7 inhibitor

USP7-797 (RAPT41) is a novel potent selective inhibitor of USP7 with IC50 of 0.44 nM.
PC-38173

FT206

USP28 inhibitor

FT206 (FT-206, FT3951206, CRT0511973) is a potent, selectivel inhibitor of USP28 with a remarkable USP28/25 selectivity.
PC-38156

XL-9872-106C

JOSD1/USP30/UCHL1 inhibitor

XL-9872-106C (XL-106C) is a potent, selective inhibitor of the deubiquitinase (DUB) JOSD1/USP30/UCHL1 with IC50 of 134/390/166 nM, respectively.
PC-38155

SB1-F-70

JOSD1/USP30/UCHL1 inhibitor

SB1-F-70 is a potent, selective inhibitor of the deubiquitinase (DUB) JOSD1/USP30/UCHL1 with IC50 of 324/400/400 nM, respectively.
PC-38072

XL177A

USP7 inhibitor

XL177A (XL-177A) is a potent, selective, irreversible USP7 inhibitor with IC50 of 0.34 nM.
PC-36022

KL001

Cryptochrome modulator

KL001 (KL-001) is a small molecule that specifically interacts with cryptochrome (CRY) and small molecule modulator of the circadian clock.
PC-35780

STD1T

USP2a inhibitor

STD1T (USP2a inhibitor STD1T) is a hit-to-lead, small-molecule inhibitor of USP2a with IC50 of 3.3 uM in Ub-AMC assays, displays no activity against USP7 at 10 uM..
PC-35682

IU1-248

USP14 inhibitor

IU1-248 (USP14 inhibitor IU1-248) is a potent, selective USP14 inhibitor with IC50 of 0.83 uM, IU1-248 is an IU1 derivative that is 10-fold more potent than IU1.
PC-35263

MF-094

USP30 inhibitor

MF-094 (MF094) is a potent, highly selective inhibitor of ubiquitin specific protease 30 (USP30) with IC50 of 0.12 uM, demonstrates <30% inhibitory activity for a panel of 22 USPs assays at 10 uM.
PC-63454

NSC112200

ZRANB1 inhibitor

NSC112200 is a chemical inhibitor of the EZH2 deubiquitinase ZRANB1 (at 10 uM), destabilizes EZH2, promotes proteasomal degradation of EZH2 and inhibits the viability of TNBC cells.

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