Gefitinib
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Catalog number1589-25
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PricePlease ask
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Size25 mg
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Alternative_nameZD-1839
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DescriptionGefitinib 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
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CAS Number184475-35-2
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Structure AvailableYes
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Salt FormNo
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Molecular FormulaC₂₂H₂₄ClFN₄O₃
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Molecular Weight446.9
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Cell PermeableYes
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Purity≥99% by HPLC
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SolubilitiesDMSO (100 mg/ml)
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HandlingProtect from light and moisture
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Tag LineAn EGFR kinase inhibitor
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Storage Condition-20°C
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Shipping ConditionRT
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Shelf Life24months
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MDL NumberMFCD04307832
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PubChem CID123631
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SMILESCOC1=C(C=C2C(=C1)N=CN=C2NC3=CC(=C(C=C3)F)Cl)OCCCN4CCOCC4
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InChiInChI=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)
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InChi KeyXGALLCVXEZPNRQ-UHFFFAOYSA-N
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MSDS AvailableYes
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Gene target
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Short nameGefitinib
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Alternative nameGefitinib
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