HBX 41108 is an inhibitor of ubiquitin-specific protease 7 (USP7) with an IC50 of 424 nM. HBX 41108 inhibits USP7-mediated p53 deubiquitination to stabilize p53 and inhibits cancer cell growth. BX 41108 can be used in cancer and diabetes research[1][2][3
Molecular Weight:
266.64
Purity:
99.61
CAS Number:
[924296-39-9]
Formula:
C13H3ClN4O
Target:
Apoptosis,Deubiquitinase,MDM-2/p53
Application Notes:
Reference compound
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