Powder: -20°C for 3 years
In solvent: -80°C for 2 years
HBx 41108 is a non-competitive, reversible inhibitor of USP7 with an IC50 of 424nM. HBx 41108 inhibited deubiquitination of p53 mediated by USP7 in a dose-dependent manner with an IC50 of 0.8μM.
Description | HBx 41108 is a non-competitive, reversible inhibitor of USP7 with an IC50 of 424nM. HBx 41108 inhibited deubiquitination of p53 mediated by USP7 in a dose-dependent manner with an IC50 of 0.8μM. |
Targets&IC50 | USP7:424nM, p53:0.8μM |
Synonyms | HBX-41108 |
Molecular Weight | 266.64 |
Formula | C13H3ClN4O |
CAS No. | 924296-39-9 |
Powder: -20°C for 3 years
In solvent: -80°C for 2 years
DMSO: 13 mg/mL
( < 1 mg/ml refers to the product slightly soluble or insoluble )
You can also refer to dose conversion for different animals. More
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HBX 41108 924296-39-9 Apoptosis Cell Cycle/Checkpoint DNA Damage/DNA Repair Ubiquitination p53 DUB DUBs inhibit Deubiquitinase Inhibitor HBX-41108 HBX41108 inhibitor