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

Cat. No. Product Name Information
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-27978

Hemi-ubistatin

Ubiquitin-proteasome system inhibitor

Hemi-ubistatin B (h-ubiB) is a small molecule inhibitor of proteasome-dependent degradation by binding the ubiquitin chain, binds ubiquitin and diubiquitin, shows strong preference for K48-linkages over K11 and K63, penetrates cancer cells and alters the cellular ubiquitin landscape.
PC-27904

USP15 inhibitor Z86

USP15 inhibitor, Wnt inhibitor

USP15 inhibitor Z86 is a small molecule USP15 inhibitor, promotes the ubiquitination and degradation of Smad2/3 and disrupts TGF-β/Smad2/3 signaling pathway, does not inhibit USP8 and USP4.
PC-26833

SGC-UBD1031

USP16/HDAC6-UBD inhibitor

SGC-UBD1031 (UBD1031) is a potent, specific dual USP16 and HDAC6 zinc-finger ubiquitin-binding domain (UBD) with SPR Kd of 48 nM and 16 nM respectively, disrupts the interaction between the C-terminus of ISG15 and USP16-UBD, as well as the interaction between ISG15 and HDAC6-UBD with IC50 of 1.7 uM and 1.5 uM in cellular assays.
PC-26806

NK192

USP7 inhibitor

NK192 is a potent, selective USP7 inhibitor with IC50 of 20 nM, shows proteome-wide specificity.
PC-26791

ZHAWOC8655

USP18 inhibitor

ZHAWOC8655 is a small molecule USP18 inhibitor with IC50 of 14.1 uM (hUSP18), disrupts the intracellular binding of USP18/ISG15.
PC-26670

Berberine chloride

USP22 inhibitor

Berberine chloride is an alkaloid with antibiotic properties, induces reactive oxygen species (ROS) generation and inhibits DNA topoisomerase, also directly binds to transcription factor Early B Cell Factor 2 (EBF2), modulate EBF2 phase separation and thermogenic function, also is a potent USP22 inhibitor, effectively suppresses Wnt pathway activation and CRC cell proliferation.

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