SJB2-043

CAS No. 63388-44-3

SJB2-043( —— )

Catalog No. M20973 CAS No. 63388-44-3

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

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 178 Get Quote
10MG 273 Get Quote
25MG 464 Get Quote
50MG 650 Get Quote
100MG 888 Get Quote
200MG 1242 Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    SJB2-043
  • Note
    Research use only, not for human use.
  • Brief Description
    SJB2-043 is an inhibitor of USP1-UAF1 ( IC50 : 544 nM).
  • Description
    SJB2-043 is an inhibitor of USP1-UAF1 ( IC50 : 544 nM).
  • In Vitro
    SJB2-043 causes a dose-dependent decrease in ubiquitin-specific protease 1 (USP1) levels and a concomitant degradation of inhibitor of DNA-binding-1 (ID1) protein in the K562 cells at a micromolar drug concentration. SJB2-043 also causes a decrease in the levels of other ID proteins, namely ID2 and ID3 in K562 cells. SJB2-043 causes a dose-dependent decrease in the number of viable K562 cells, with an EC50 of approximately 1.07 μM. Moreover, SJB2-043 induces apoptosis of K562 cells in a dose-dependent manner.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Proteasome/Ubiquitin
  • Target
    DUB
  • Recptor
    USP1-UAF1
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    63388-44-3
  • Formula Weight
    275.26
  • Molecular Formula
    C17H9NO3
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO:3.33 mg/mL (12.10 mM)
  • SMILES
    O=C1c2ccccc2C(=O)c2oc(-c3ccccc3)nc21
  • Chemical Name
    2-Phenyl-naphth[23-d]oxazole-49-dione

Shipping & Storage Information

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

Reference

1.Jussara Maria Goncalves et al. The Role of the Complex USP1/WDR48 in Differentiation and Proliferation Processes in Cancer Stem Cells.[J]. Current stem cell research & therapy 2017.
molnova catalog
related products
  • TCID

    TCID is a selective ubiquitin C-terminal hydrolase-L3 (UCH-L3) inhibitor with IC50 of 0.6 uM.

  • HBX 41108

    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.

  • Wu-5

    Wu-5 is a potent USP10 inhibitor that inhibits FLT3 and AMPK pathways, promoting the breakdown of FLT3-ITD and inducing apoptosis.