Gefitinib

  • Catalog number
    1589-25
  • Price
    Please ask
  • Size
    25 mg
  • Alternative_name
    ZD-1839
  • Description
    Gefitinib was found to be a potent inhibitor of EGFR kinase (Ki = 0.40 nM), but much weaker against ErbB-2 kinase (Ki = 870 nM) and ErbB-4 kinase (Ki = 1.1 µM). The IC₅₀ values for Gefitinib to inhibit HT-29 and LoVo cell growth were 23.6 - >100 µM and 7.3 - 48.5 µM, respectively, when the exposure times are from 18 hours to 3 days. The IC₅₀ values of Gefitinib to the breast cancer cell lines BT20, HCC1937, MDA-MB-231, BT474, and SKBR3 are 15.5±1.4, 8.4±1.5, 20.7±1.1, 0.25±0.05, 0.88±0.31 µM, respectively
  • CAS Number
    184475-35-2
  • Structure Available
    Yes
  • Salt Form
    No
  • Molecular Formula
    C₂₂H₂₄ClFN₄O₃
  • Molecular Weight
    446.9
  • Cell Permeable
    Yes
  • Purity
    ≥99% by HPLC
  • Solubilities
    DMSO (100 mg/ml)
  • Handling
    Protect from light and moisture
  • Tag Line
    An EGFR kinase inhibitor
  • Storage Condition
    -20°C
  • Shipping Condition
    RT
  • Shelf Life
    24months
  • MDL Number
    MFCD04307832
  • PubChem CID
    123631
  • SMILES
    COC1=C(C=C2C(=C1)N=CN=C2NC3=CC(=C(C=C3)F)Cl)OCCCN4CCOCC4
  • InChi
    InChI=1S/C22H24ClFN4O3/c1-29-20-13-19-16(12-21(20)31-8-2-5-28-6-9-30-10- 7-28)22(26-14-25-19)27-15-3-4-18(24)17(23)11-15/h3-4,11-14H,2,5-10H2,1H3,(H,25,26,27)
  • InChi Key
    XGALLCVXEZPNRQ-UHFFFAOYSA-N
  • MSDS Available
    Yes
  • Gene target
  • Short name
    Gefitinib
  • Alternative name
    Gefitinib
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