CCF642

CAS No. 346640-08-2

CCF642 ( CCF-642; CCF 642; CCF642 )

Catalog No. M17489 CAS No. 346640-08-2

CCF642 is a novel PDI-inhibiting compound with antimyeloma activity.

Purity : 98%

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 39 In Stock
5MG 69 In Stock
10MG 95 In Stock
25MG 186 In Stock
50MG 332 In Stock
100MG 478 In Stock
500MG 1062 In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    CCF642
  • Note
    Research use only, not for human use.
  • Brief Description
    CCF642 is a novel PDI-inhibiting compound with antimyeloma activity.
  • Description
    CCF-642 is a protein disulfide isomerase (PDI) inhibitor. CCF642 exhibited a submicromolar IC50 in 10 of 10 multiple myeloma cell lines. In vitro, CCF642 inhibited PDI reductase activity about 100-fold more potently than the structurally distinct established inhibitors PACMA 31 and LOC14. CCF642 displayed potent efficacy in an aggressive syngeneic mouse model of multiple myeloma and prolonged the lifespan of C57BL/KaLwRij mice engrafted with 5TGM1-luc myeloma, an effect comparable to the first-line multiple myeloma therapeutic bortezomib.
  • Synonyms
    CCF-642; CCF 642; CCF642
  • Pathway
    Angiogenesis
  • Target
    EGFR
  • Recptor
    protein disulfide isomerases
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    346640-08-2
  • Formula Weight
    378.45
  • Molecular Formula
    C15H10N2O4S3
  • Purity
    98%
  • Solubility
    DMSO : ≥ 30 mg/mL; 79.27 mM
  • SMILES
    S1C(=S)N(C(=O)/C/1=C\c1ccc(s1)[N+](=O)[O-])c1ccc(cc1)OC
  • Chemical Name
    3-(4-Methoxyphenyl)-5-[(5-nitro-2-thienyl)methylene]-2-thioxo-4-thiazolidinone

Shipping & Storage Information

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

Reference

1.Vatolin S et al. Novel Protein Disulfide Isomerase Inhibitor with Anticancer Activity in Multiple Myeloma. Cancer Res. 2016 Jun 1;76(11):3340-50.
molnova catalog
related products
  • FRAX1036

    FRAX-1036 is a effective and selective PAK1 inhibitor.

  • Erlotinib hydrochlor...

    Erlotinib (CP-358774;OSI-774;NSC 718781) is a potent, selective inhibitor of EGFR with IC50 of 2 nM.

  • 7,8-Dihydroxyflavone

    7, 8-Dihydroxyflavone (7, 8-DHF) is a naturally-occurring flavone and exist in Tridax procumbens, Godmania aesculifolia, and primula tree leaves.