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

Cat. No. Product Name Information
PC-20472

IU1-206

USP14 inhibitor

IU1-206 is a IU1 derivative with more potent activity against USP14, 10-fold more potent than IU1 and is comparable to the IU1-47.
PC-20403

PR-619

DUBs inhibitor

PR-619 (PR619) is a broad-spectrum, reversible deubiquitinating enzymes (DUBs) inhibitor with IC50 of 3.93 uM-8.87 uM.
PC-20202

HBX41108

USP7 inhibitor

HBX41108 is a specific small-molecule inhibitor of USP7/HAUSP ubiquitin protease with IC50 of 424 nM for inhibition of Ub-AMC hydrolysis by USP7.
PC-20190

USP14 inhibitor 3

USP14 inhibitor

USP14-IN-3 is a specific small molecule USP14 inhibitor with IC50 of <0.5 uM.
PC-20189

USP14 inhibitor 2

USP14 inhibitor

USP14-IN-2 is a specific small molecule USP14 inhibitor with IC50 of <0.5 uM.
PC-20186

USP14 inhibitor 1

USP14 inhibitor

USP14-IN-1 is a specific small molecule USP14 inhibitor with IC50 of 0.5 uM.
PC-20185

IU2-6

USP14 inhibitor

IU2-6 is a small molecule USP14 inhibitor, shows 74% inhibition at 8 uM.
PC-20184

GSK2643943A

USP20 inhibitor

GSK2643943A is a specific, cell penetrant small molecule inhibitor of deubiquitinating enzyme USP20 with IC50 of 160 nM (USP20/Ub-Rho).
PC-20004

TG2-179-1

BAP1 inhibitor

TG2-179-1 is a potent, selective and covalently inhibitor of deubiquitinase (DUB) BRCA1-associated protein-1 (BAP1), covalently binds to the active site of BAP1 (Cys91), exhibits potent cytotoxic activity against colon cancer cells.
PC-20001

CAS-12290-201

VCPIP1 inhibitor

CAS-12290-201 is a potent and selective inhibitor of deubiquitinating enzyme (DUB) VCPIP1 with IC50 of 70 nM, covalently and specificly targets the catalytic cysteine of VCPIP1 with little to no activity toward other cellular DUBs.
PC-49863

BAY-728

BAY-805 negative control

BAY-728 (BAY728, (S)-BAY-805) is a less potent enantiomer and negative control compound of BAY-805, which is a potent and selective Inhibitor of USP21.
PC-49862

BAY-805

USP21 inhibitor

BAY-805 (BAY805) is the first highly potent, selective and non-covalent USP21 inhibitor with IC50 of 6 nM and 2 nM in HTRF and Ub-rhodamine biochemical assays (hUSP21), respectively.

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