HBX 41108

CAS No. 924296-39-9

HBX 41108 ( HBX-41108 )

Catalog No. M27424 CAS No. 924296-39-9

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.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 61 Get Quote
5MG 102 Get Quote
10MG 170 Get Quote
25MG 402 Get Quote
50MG 593 Get Quote
100MG 845 Get Quote
200MG Get Quote Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    HBX 41108
  • Note
    Research use only, not for human use.
  • Brief 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.
  • 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.
  • Synonyms
    HBX-41108
  • Pathway
    Proteasome/Ubiquitin
  • Target
    DUB
  • Recptor
    Bax;Bcl-2;Caspase-3
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    924296-39-9
  • Formula Weight
    266.6
  • Molecular Formula
    C13H3ClN4O
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Clc1ccc-2c(c1)C(=O)c1nc(C#N)c(nc-21)C#N
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1.Zhou D, et al. Antiproliferative steroidal glycosides from rhizomes of Polygonatum sibiricum. Phytochemistry. 2019;164:172-183.
molnova catalog
related products
  • XL 188

    XL188 (XL-188) is a potent, selective, non-covalent active-site inhibitor of USP7 with IC50 of 90 nM and 193 nM for USP7 full length enzyme and catalytic domain, respectively.

  • FT-671

    FT-671 is a novel potent, specific, non-covalent USP7 inhibitor with Kd of 65 nM (USP7 catalytic domain).

  • KL001

    KL001 (KL-001) is a small molecule that specifically interacts with cryptochrome (CRY) and small molecule modulator of the circadian clock.