CC-885

CAS No. 1010100-07-8

CC-885( CC 885 | CC885 )

Catalog No. M10068 CAS No. 1010100-07-8

CC-885 (CC 885, CC885) is a novel E3 ligase cereblon (CRBN) modulator with potent anti-tumour activity mediated through the degradation of GSPT1.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 135 In Stock
5MG 116 In Stock
10MG 163 In Stock
25MG 306 In Stock
50MG 485 In Stock
100MG 706 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    CC-885
  • Note
    Research use only, not for human use.
  • Brief Description
    CC-885 (CC 885, CC885) is a novel E3 ligase cereblon (CRBN) modulator with potent anti-tumour activity mediated through the degradation of GSPT1.
  • Description
    CC-885 (CC 885, CC885) is a novel E3 ligase cereblon (CRBN) modulator with potent anti-tumour activity mediated through the degradation of GSPT1; The anti-tumour activity of CC-885 is mediated through the cereblon-dependent ubiquitination and degradation of the translation termination factor GSPT1; promotes both the in vivo and in vitro ubiquitination of GSPT1 by cereblon and decreases the protein half-life of GSPT1.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    CC 885 | CC885
  • Pathway
    PROTACs
  • Target
    E3 Ligase Ligand
  • Recptor
    E3 Ligase Ligand
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    1010100-07-8
  • Formula Weight
    440.9
  • Molecular Formula
    C22H21ClN4O4
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 67.5 mg/mL (153.10 mM)
  • SMILES
    O=C(NCC1=CC2=C(C(N(C(CC3)C(NC3=O)=O)C2)=O)C=C1)NC4=CC=C(C)C(Cl)=C4
  • Chemical Name
    N-(3-chloro-4-methylphenyl)-N'-[[2-(2,6-dioxo-3-piperidinyl)-2,3-dihydro-1-oxo-1H-isoindol-5-yl]methyl]-urea

Shipping & Storage Information

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

Reference

1. Collins I, et al. Biochem J. 2017 Mar 15;474(7):1127-1147. 2. Matyskiela ME, et al. Nature. 2016 Jul 14;535(7611):252-7. 3. Hansen JD, et al. J Med Chem. 2017 Apr 13. doi: 10.1021/acs.jmedchem.6b01911.
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