Allitinib

CAS No. 897383-62-9

Allitinib ( AST-1306; ALS 1306 )

Catalog No. M26612 CAS No. 897383-62-9

Allitinib (AST-1306) has anti-cancer activity,and it is an irreversible EGFR and ErbB2 inhibitor with IC50s of 0.5 and 3 nM, respectively.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
5MG 174 Get Quote
10MG 259 Get Quote
25MG 438 Get Quote
50MG 624 Get Quote
100MG 867 Get Quote
500MG 1737 Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Allitinib
  • Note
    Research use only, not for human use.
  • Brief Description
    Allitinib (AST-1306) has anti-cancer activity,and it is an irreversible EGFR and ErbB2 inhibitor with IC50s of 0.5 and 3 nM, respectively.
  • Description
    Allitinib (AST-1306) has anti-cancer activity,and it is an irreversible EGFR and ErbB2 inhibitor with IC50s of 0.5 and 3 nM, respectively. (In Vitro):AST1306 (AST-1306; 0.19-6.25 μM; 72 hours) inhibit the growth of HIH3T3-EGFR T790M/L858R cells. AST1306 (0.001-1.0 μM; 4 hours) is more than 3000-fold selective for ErbB family kinases over other kinase families. AST1306 inhibits the activation of tyrosine kinases and downstream signaling pathways in A549 cells, Calu-3 cells and SK-OV-3 cells,and dose-dependently and markedly inhibits EGF-induced EGFR phosphorylation in A549 cells.(In Vivo):AST1306 (AST-1306; oral; 25-100 mg/kg) significantly inhibited tumor growth in SK-OV-3 and Calu-3 xenograft models.
  • Synonyms
    AST-1306; ALS 1306
  • Pathway
    Angiogenesis
  • Target
    EGFR
  • Recptor
    A1
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    897383-62-9
  • Formula Weight
    448.9
  • Molecular Formula
    C24H18ClFN4O2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    Fc1cccc(COc2ccc(Nc3ncnc4ccc(NC(=O)C=C)cc34)cc2Cl)c1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1.Aurelio L, et al. Allosteric modulators of the adenosine A1 receptor: synthesis and pharmacological evaluation of 4-substituted 2-amino-3-benzoylthiophenes. J Med Chem. 2009 Jul 23;52(14):4543-7.
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