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

Cat. No. Product Name Information
PC-72535

HBX-90659

USP8 inhibitor

HBX-90659 (compound 22 e) is a potent, selective USP8 inhibitor with IC50 of 0.28 uM, with no effect on USP7 (IC50 of >100 uM).
PC-72534

USP8 inhibitor RA-9

USP8 inhibitor

USP8 inhibitor RA-9 is a small molecule USP8 inhibitor.
PC-72414

USP5 inhibitor 64

USP5 inhibitor

USP5 inhibitor 64 is a selective chemical probe (inhibitor) against USP5 deubiquitinase, binds to the USP5 ZnF-UBD (zinc-finger ubiquitin binding domain) with KD of 2.8 uM.
PC-72297

iBAP

BAP1 inhibitor

iBAP (BAP1 inhibitor I) is a first-in-class inhibitor of the catalytic activity of BAP1 histone H2A deubiquitinase complex with IC50 of 0.5-1 uM in vitro,
PC-72296

iBAP-II

BAP1 inhibitor

iBAP-II (BAP1 inhibitor II) is a next-generation, specific small molecule inhibitor of BAP1 histone H2A deubiquitinase activity with IC50 of <0.1 ug/mL.
PC-72255

USP30 inhibitor Q14 peptide

USP30 inhibitor

USP30 inhibitor Q14 peptide is a potent peptide inhibitor of USP30 with IC50 of 57.2 nM, inhibits the deubiquitinating activities of USP30, increases mitophagy.
PC-72254

USP30Inh-1

USP30 inhibitor

USP30Inh-1 is a potent, selective small molecule USP30 inhibitor with IC50 of 15-30 nM (inhibition of USP30-mediated cleavage of Ub-Rho110).
PC-72253

FT385

USP30 inhibitor

FT385 (FT3967385) is a potent, selective USP30 inhibitor with biochemical IC50 of 1.5 nM.
PC-72252

USP30 inhibitor Compound 39

USP30 inhibitor

USP30 inhibitor Compound 39 (CMPD-39) is a highly selective inhibitor of USP30 with IC50 of 20 nM in an in vitro assay of enzyme activity, >100-fold selectivity over other DUBs.
PC-72221

MT16-205

UCHL1 inhibitor

MT16-205 (MT 16-205) is a potent, selective, covalent UCHL1 inhibitor with IC50 of 600 nM, no inhibition agianst UCHL3 (IC50>10 uM).
PC-72220

UCHL1 inhibitor 27

UCHL1 inhibitor

UCHL1 inhibitor 27 is a potent, selective, covalent UCHL1 inhibitor with IC50 of 90 nM.
PC-72219

IMP-1710

UCHL1 inhibitor

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

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