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HBX 41108

HBX 41108 is a reversible, non-competitive USP7 inhibitor with an IC50 of 424 nM, which effectively blocks USP7-mediated p53 deubiquitination (IC50 = 0.8 μM) . This compound is a valuable research tool for studying the p53 pathway and USP7 biology in cancer and neurodegenerative disease models, both in vitro and in vivo.

Product Specifications

CAS Number

924296-39-9

Product Name Alternative

Apoptosis, Deubiquitinase, DUBs, Inhibitor, HBX 41108, HBX41108, HBX-41108, p53, inhibit, USP7

Field of Research

Cell Biology, Molecular Biology, Protein Biochemistry

Purity

95.63% (May vary between batches)

Solubility

DMSO:60 mg/mL (225.02 mM) ;10% DMSO+40% PEG300+5% Tween 80+45% Saline:1 mg/mL (3.75 mM)

Smiles

Clc1ccc-2c (c1) C (=O) c1nc (C#N) c (nc-21) C#N

Molecular Formula

C13H3ClN4O

Molecular Weight

266.64

Storage Conditions

-20°C

Notes

For research use only.

Available Sizes

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