Pelitinib

CAS No. 257933-82-7

Pelitinib ( EKB-569;WAY-EKB 569;EKB569;EKB 569 )

Catalog No. M13779 CAS No. 257933-82-7

A potent, selective, orally active, irreversible inhibitor of EGFR with IC50 of 80 nM.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 39 In Stock
10MG 55 In Stock
25MG 96 In Stock
50MG 120 In Stock
100MG 178 In Stock
500MG 441 In Stock
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Biological Information

  • Product Name
    Pelitinib
  • Note
    Research use only, not for human use.
  • Brief Description
    A potent, selective, orally active, irreversible inhibitor of EGFR with IC50 of 80 nM.
  • Description
    A potent, selective, orally active, irreversible inhibitor of EGFR with IC50 of 80 nM; inhibits autophosphorylation of the cytoplasmic domain of HER-2 with IC50 of 1.23 uM; shows 1-3 orders of magnitude higher IC50 value for Src, Cdk4, c-Met, Raf, and MEK/ERK; inhibits proliferation in NHEK, A431, and MDA-468 cells (IC50= 61, 125, and 260 nM, respectively); potently inhibits the EGFR phosphorylation in A431 xenografts, suppresses tumorigenesis in APCMin/+ mice.Lung Cancer Phase 2 Clinical
  • Synonyms
    EKB-569;WAY-EKB 569;EKB569;EKB 569
  • Pathway
    Angiogenesis
  • Target
    EGFR
  • Recptor
    EGFR;HER2/ErbB2;MEK;Raf;Src
  • Research Area
    Cancer
  • Indication
    Lung Cancer

Chemical Information

  • CAS Number
    257933-82-7
  • Formula Weight
    467.92
  • Molecular Formula
    C24H23ClFN5O2
  • Purity
    >98% (HPLC)
  • Solubility
    DMSO: 16 mg/mL
  • SMILES
    O=C(NC1=C(OCC)C=C2N=CC(C#N)=C(NC3=CC=C(F)C(Cl)=C3)C2=C1)/C=C/CN(C)C
  • Chemical Name
    2-Butenamide, N-[4-[(3-chloro-4-fluorophenyl)amino]-3-cyano-7-ethoxy-6-quinolinyl]-4-(dimethylamino)-, (2E)-

Shipping & Storage Information

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

Reference

1. Wissner A, et al. J Med Chem. 2003 Jan 2;46(1):49-63.
2. Nunes M, et al. Mol Cancer Ther. 2004 Jan;3(1):21-7.
3. Torrance CJ, et al. Nat Med. 2000 Sep;6(9):1024-8.
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