Alflutinib

CAS No. 1869057-83-9

Alflutinib( AST2818 | AST-2818 | ASK120067 )

Catalog No. M12888 CAS No. 1869057-83-9

Alflutinib (AST-2818, ASK120067) is a third generation EGFR mutation selective tyrosine kinase inhibitor.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 155 In Stock
5MG 123 In Stock
10MG 187 In Stock
25MG 376 In Stock
50MG 554 In Stock
100MG 731 In Stock
200MG 1042 In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    Alflutinib
  • Note
    Research use only, not for human use.
  • Brief Description
    Alflutinib (AST-2818, ASK120067) is a third generation EGFR mutation selective tyrosine kinase inhibitor.
  • Description
    Alflutinib (AST-2818, ASK120067) is a third generation EGFR mutation selective tyrosine kinase inhibitor, inhibits EGFR active mutations as well as T790M acquired resistant mutation.Lung Cancer Phase 1 Clinical.
  • In Vitro
    Firmonertinib is designed to inhibit EGFR active mutations as well as the T790M acquired resistant mutation.
  • In Vivo
    ——
  • Synonyms
    AST2818 | AST-2818 | ASK120067
  • Pathway
    Angiogenesis
  • Target
    EGFR
  • Recptor
    EGFR
  • Research Area
    Cancer
  • Indication
    Lung Cancer

Chemical Information

  • CAS Number
    1869057-83-9
  • Formula Weight
    568.605
  • Molecular Formula
    C28H31F3N8O2
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    CN(C)CCN(C)c1nc(OCC(F)(F)F)c(Nc2nccc(n2)c3cn(C)c4ccccc34)cc1NC(=O)C=C
  • Chemical Name
    N-(2-((2-(dimethylamino)ethyl)(methyl)amino)-5-((4-(1-methyl-1H-indol-3-yl)pyrimidin-2-yl)amino)-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)acrylamide

Shipping & Storage Information

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

Reference

1. PCT Int. Appl. (2017), WO 2017152707 A1 20170914.
molnova catalog
related products
  • Desmethyl Erlotinib

    OSI-420 is the active metabolite of Erlotinib (EGFR inhibitor with IC50 of 2 nM).

  • CHMFL-EGFR-202

    CHMFL-EGFR-202 is a potent, irreversible inhibitor of EGFR mutant kinase (IC50s: 5.3 nM and 8.3 nM for drug-resistant mutant EGFR T790M and WT EGFR kinases).

  • EGFR-IN-8

    EGFR-IN-8 can be a promising candidate for further development to target EGFR TKI-resistant NSCLC. EGFR-IN-8 is a dual EGFR and c-Met inhibitor.