EGFR-IN-11

CAS No. 2463200-44-2

EGFR-IN-11( —— )

Catalog No. M32907 CAS No. 2463200-44-2

EGFR-IN-11 is a selective inhibitor of EGFR-tyrosine kinase and induces cell apoptosis. EGFR-IN-11 inhibits triple mutant EGFRL858R/T790M/C797S with an IC50 of 18 nM and arrests cell cycle at G0/G1.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
1 mL x 10 mM in DMSO 100 In Stock
5MG 79 In Stock
10MG 134 In Stock
25MG 212 In Stock
50MG 288 In Stock
100MG 383 In Stock
200MG Get Quote In Stock
500MG Get Quote In Stock
1G Get Quote In Stock

Biological Information

  • Product Name
    EGFR-IN-11
  • Note
    Research use only, not for human use.
  • Brief Description
    EGFR-IN-11 is a selective inhibitor of EGFR-tyrosine kinase and induces cell apoptosis. EGFR-IN-11 inhibits triple mutant EGFRL858R/T790M/C797S with an IC50 of 18 nM and arrests cell cycle at G0/G1.
  • Description
    EGFR-IN-11 is a fourth-generation EGFR-tyrosine kinase inhibitor (EGFR-TKI) with an IC50 of 18 nM for triple mutant EGFRL858R/T790M/C797S. EGFR-IN-11 significantly suppresses the EGFR phosphorylation, induce the apoptosis, and arrest cell cycle at G0/G1.
  • In Vitro
    EGFR-IN-11 (Compound D9; 0.0001-10 μM; 72 hours) shows significantly potent anti-proliferation against HCC827 and H1975 cell lines with IC50s of 0.88 nM and 0.20 μM, respectively. EGFR-IN-11 (0.01-1.00 μM for HCC827 cells; 0.1-10.00 μM for H1975 and A549 cells; 8 hours) suppresses EGFR phosphorylation in a concentration-dependent manner in the HCC827, H1975 and A549 cell line.EGFR-IN-11 (1 μM; 24 h) potently induces the apoptosis of HCC827 cells.EGFR-IN-11 (1 μM; 24 h) induces cell cycle arrests in HCC827 cell.Cell Proliferation Assay Cell Line:Human lung cancer cell lines HCC827 (EGFRDel E746-A750), H1975 (EGFRL858R/T790M) and A549 (EGFRWT); epidermoid carcinoma cell line A431 (EGFRWT) Concentration:0.0001, 0.0003, 0.001, 0.003, 0.01, 0.1, 1, 10 μM Incubation Time:72 hours Result:Inhibited HCC827 H1975 A549 cells proliferation with IC50s of 0.88±0.09 nM, 0.20±0.01 μM, 2.91±0.61 μM, and >10 μM, respectively.Western Blot Analysis Cell Line:HCC827, H1975 and A549 cells Concentration:1.00, 0.10 and 0.01 μM for HCC827 cells; 10.00, 1.00 and 0.10 μM for H1975 and A549 cells Incubation Time:8 hours Result:Suppressed EGFR phosphorylation in a concentration-dependent manner. EGFR phosphorylation in the HCC827 cell line was more remarkably suppressed than in the H1975 and A549 cell lines. Apoptosis Analysis Cell Line:HCC827 cells Concentration:1 μM Incubation Time:24 hours Result:The percentages of apoptotic cells is 56.91%.Cell Cycle Analysis Cell Line:HCC827 cells Concentration:1 μM Incubation Time:24 hours Result:The number of HCC827 cells in G0/G1 phase was increased significantly.
  • In Vivo
    ——
  • Synonyms
    ——
  • Pathway
    Angiogenesis
  • Target
    EGFR
  • Recptor
    EGFR
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    2463200-44-2
  • Formula Weight
    573.71
  • Molecular Formula
    C29H35N9O2S
  • Purity
    >98% (HPLC)
  • Solubility
    In Vitro:?DMSO : 125 mg/mL (217.88 mM; Ultrasonic )
  • SMILES
    CN1CCN(CC1)c1ccc(Nc2ncc3nc(Nc4ccccc4)n([C@@H]4CCN(C4)S(=O)(=O)C4CC4)c3n2)cc1
  • Chemical Name
    ——

Shipping & Storage Information

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

Reference

1. Lei H, et al. Discovery of novel 9-heterocyclyl substituted 9H-purines as L858R/T790M/C797S mutant EGFR tyrosine kinase inhibitors. Eur J Med Chem. 2019 Nov 16:111888.?
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