Product Data Sheet

PF-2341066 (Crizotinib)

Catalog No. A10712

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PF-2341066 (Crizotinib) is an inhibitor of the c-Met kinase and the NPM-ALK. PF-2341066 inhibited cell proliferation in ALK-positive ALCL cells (IC50s=30 nM).
Adooq's PF-2341066 (Crizotinib) has been cited by 7 publications
  • Sang-Yun Lee, .et al. , J Exp Clin Cancer Res, 2023, Nov 22;42(1):309 PMID: 37993887
  • Reiko Watanabe, .et al. , J Med Chem, 2021, Mar 11;64(5):2725-2738 PMID: 33619967
  • Yu B, .et al. , J Sep Sci, 2020, Jan 22 PMID: 31970927
  • Li Li, .et al. , Leukemia Res, 2019, 78:12-20 PMID: 30660961
  • Li T, .et al. , Oncogene, 2018, Nov;37(47):6180-6194 PMID: 30013190
  • Saki Omote, .et al. , Sci Rep, 2018, 8: 9237 PMID: 29915248
  • Arakawa H, .et al. , J Pharm Sci, 2017, Sep;106(9):2899-2903 PMID: 28336299
  • Chemical Information
    Catalog NumA10712
    M. Wt450.3
    FormulaC21H22Cl2FN5O
    Purity>98%
    Storageat -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
    CAS No.877399-52-5
    Synonyms
    SMILESC[C@H](C1=C(C=CC(=C1Cl)F)Cl)OC2=C(N=CC(=C2)C3=CN(N=C3)C4CCNCC4)N
    Biological Activity
    DescriptionPF-2341066 (Crizotinib) is an inhibitor of the c-Met kinase and the NPM-ALK. PF-2341066 inhibited cell proliferation in ALK-positive ALCL cells (IC50s=30 nM).
    Targets
    TargetValue
    Solubility
    In vitro (25°C) DMSO8 mg/mL (17.76 mM)
    WaterInsoluble
    EthanolInsoluble
    In vivo5% DMSO+30% PEG 300+dd H2O4 mg/mL
    * <1 mg/ml means slightly soluble or insoluble.
    * Please note that Adooq tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.
    Preparing Stock Solutions
    Concentration / Solvent Volume / Mass1 mg5 mg10 mg
    0.1 mM22.21 mL111.04 mL222.07 mL
    0.5 mM4.44 mL22.21 mL44.41 mL
    1 mM2.22 mL11.1 mL22.21 mL
    5 mM0.44 mL2.22 mL4.44 mL
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    SHIPPING AND STORAGE
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