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
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2MG 120 Get Quote
5MG 186 Get Quote
10MG 320 Get Quote
25MG 491 Get Quote
50MG 679 Get Quote
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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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