SNIPER(AR)-51

CAS No. 2113688-43-8

SNIPER(AR)-51( SNIPER AR-51 )

Catalog No. M13362 CAS No. 2113688-43-8

SNIPER(AR)-51 is a specific and nongenetic, protein degradation inducer of androgen receptor, consistiong of AR ligand and IAP ligand and linker; induces proteasomal degradation of AR and shows effective protein knockdown activity.

Purity : >98% (HPLC)

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Biological Information

  • Product Name
    SNIPER(AR)-51
  • Note
    Research use only, not for human use.
  • Brief Description
    SNIPER(AR)-51 is a specific and nongenetic, protein degradation inducer of androgen receptor, consistiong of AR ligand and IAP ligand and linker; induces proteasomal degradation of AR and shows effective protein knockdown activity.
  • Description
    SNIPER(AR)-51 is a specific and nongenetic, protein degradation inducer of androgen receptor, consistiong of AR ligand and IAP ligand and linker; induces proteasomal degradation of AR and shows effective protein knockdown activity; inhibits AR-mediated gene expression and proliferation of androgen-dependent prostate cancer cells, and efficiently induces caspase activation and apoptosis in prostate cancer cells.
  • In Vitro
    ——
  • In Vivo
    ——
  • Synonyms
    SNIPER AR-51
  • Pathway
    PROTACs
  • Target
    PROTAC
  • Recptor
    PROTAC
  • Research Area
    Cancer
  • Indication
    ——

Chemical Information

  • CAS Number
    2113688-43-8
  • Formula Weight
    984.226
  • Molecular Formula
    C55H65N7O8S
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    C[C@H](NC)C(N[C@@H](C1CCCCC1)C(N2[C@H](C3=NC(C(C4=CC=CC(OCCOCCOCCOCCOC5=CC=C(CN6C(C)=C(C#N)C(C7=CC=C(C#N)C=C7)=C6C)C=C5)=C4)=O)=CS3)CCC2)=O)=O
  • Chemical Name
    (S)-N-((S)-2-((S)-2-(4-(3-(2-(2-(2-(2-(4-((3-cyano-4-(4-cyanophenyl)-2,5-dimethyl-1H-pyrrol-1-yl)methyl)phenoxy)ethoxy)ethoxy)ethoxy)ethoxy)benzoyl)thiazol-2-yl)pyrrolidin-1-yl)-1-cyclohexyl-2-oxoethyl)-2-(methylamino)propanamide

Shipping & Storage Information

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

Reference

1. Shibata N, et al. J Med Chem. 2017 Jun 23. doi: 10.1021/acs.jmedchem.7b00168.
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