HBX-19818

CAS No. 1426944-49-1

HBX-19818( HBX19818 | HBX-19818 | HBX 19818 )

Catalog No. M11802 CAS No. 1426944-49-1

HBX-19818 is a potent, selective USP7 inhibitor with IC50 of 28.1 uM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 82 In Stock
5MG 73 In Stock
10MG 113 In Stock
25MG 187 In Stock
50MG 261 In Stock
100MG 365 In Stock
200MG 518 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    HBX-19818
  • Note
    Research use only, not for human use.
  • Brief Description
    HBX-19818 is a potent, selective USP7 inhibitor with IC50 of 28.1 uM.
  • Description
    HBX-19818 is a potent, selective USP7 inhibitor with IC50 of 28.1 uM; exhibits high selectivity over other USP members, such as USP8, USP5, USP2, and USP20 (IC50 >200 uM), and no activity against UCH-L1, UCH-L3 and SENP1; reduces HCT116 cell proliferation, induces caspase activity and PARP cleavage, and arrests HCT116 cancer cells in G1.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    HBX19818 | HBX-19818 | HBX 19818
  • Pathway
    Proteasome/Ubiquitin
  • Target
    DUB
  • Recptor
    DUB
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1426944-49-1
  • Formula Weight
    421.96
  • Molecular Formula
    C25H28ClN3O
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 3.5 mg/mL; DMSO: 5.3 mg/mL (Need ultrasonic)
  • SMILES
    O=C(C1=CC2=C(Cl)C3=C(CCCC3)N=C2C=C1)NCCCN(C)CC4=CC=CC=C4
  • Chemical Name
    2-Acridinecarboxamide, 9-chloro-5,6,7,8-tetrahydro-N-[3-[methyl(phenylmethyl)amino]propyl]-

Shipping & Storage Information

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

Reference

1. Reverdy C, et al. Chem Biol. 2012 Apr 20;19(4):467-77.
molnova catalog
related products
  • BRD 0476

    BRD 0476 (ML187) is a selective, moderate inhibitor of ubiquitin-specific peptidase 9X (USP9X).

  • Vialinin A

    Vialinin A (Terrestrin A), a p-terphenyl compound, exhibits antioxidant properties and acts as a potent inhibitor of TNF-α, USP4, USP5, and sentrin/SUMO-specific protease 1 (SENP1).

  • SJB2-043

    SJB2-043 is an inhibitor of ?USP1-UAF1?( IC50 : 544 nM).