Render Target: STATIC
Render Timestamp: 2024-12-26T10:59:03.557Z
Commit: f2d32940205a64f990b886d724ccee2c9935daff
XML generation date: 2024-09-20 06:19:14.384
Product last modified at: 2024-12-17T19:03:57.836Z
Cell Signaling Technology Logo
1% for the planet logo
PDP - Template Name: Chemical Modulators
PDP - Template ID: *******c501c72

Imatinib #9084

    Product Information

    Product Usage Information

    Imatinib is supplied as a lyophilized powder. For a 10 mM stock, reconstitute the 5 mg in 847.9 μl DMSO. Working concentrations and length of treatment can vary depending on the desired effect, but it is typically used at 1-10 μM for 1-2 hours. Soluble in DMSO at 100 mg/ml; poorly soluble in ethanol. Soluble in water at 200 mg/ml.

    Storage

    Store lyophilized or in solution at -20ºC, desiccated. Protect from light. In lyophilized form, the chemical is stable for 24 months. Once in solution, use within 3 months to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

    Product Description

    Molecular Weight 589.71 g/mol
    Purity >99%
    Molecular Formula C29H31N7O + CH4SO3
    CAS 220127-57-1
    Solubility Soluble in DMSO at 100mg/ml and H2O at 200mg/ml.

    Background

    Imatinib is a tyrosine kinase (TK) inhibitor that is a relatively specific ATP-binding site antagonist of Bcr-Abl, PDGF receptor, and c-Kit TKs (1-3). Results are encouraging in chronic myeloid leukemia (CML) clinical trials and imatinib has become a paradigm for targeted cancer therapeutics (4-6). Signal transduction through phospho-tyrosine pathways has been studied extensively, and tyrosine phosphorylation has been linked to multiple cell growth and differentiation pathways (7-9). Because the observed leukemic state of CML is dependent on the intact Bcr-Abl tyrosine kinase activity, extensive work has been done to identify substrates of Bcr-Abl and thus possible mechanisms leading to a myeloid expansion. Many groups have characterized prominent tyrosine-phosphorylated protein substrates in both CML blasts and Bcr-Abl-expressing cell lines, including SHIP, c-Cbl, Dok, Shc, and CrkL (10-15). In addition, key signal transduction pathways involving PI3 kinase, Ras, Myc, and Stat5 are also activated in a Bcr-Abl kinase-dependent manner (16).
    1. Buchdunger, E. et al. (1996) Cancer Res 56, 100-4.
    2. Heinrich, M.C. et al. (2000) Blood 96, 925-32.
    3. Druker, B.J. et al. (1996) Nat Med 2, 561-6.
    4. Mauro, M.J. and Druker, B.J. (2001) Curr Oncol Rep 3, 223-7.
    5. Druker, B.J. et al. (2001) N Engl J Med 344, 1031-7.
    6. Druker, B.J. et al. (2001) N Engl J Med 344, 1038-42.
    7. Blume-Jensen, P. and Hunter, T. (2001) Nature 411, 355-65.
    8. Ullrich, A. and Schlessinger, J. (1990) Cell 61, 203-12.
    9. Cantley, L.C. et al. (1991) Cell 64, 281-302.
    10. ten Hoeve, J. et al. (1994) Blood 84, 1731-6.
    11. Matsuguchi, T. et al. (1994) J Biol Chem 269, 5016-21.
    12. Carpino, N. et al. (1997) Cell 88, 197-204.
    13. Sattler, M. et al. (1997) Oncogene 15, 2379-84.
    14. Di Cristofano, A. et al. (1998) J Biol Chem 273, 4827-30.
    15. Wisniewski, D. et al. (1999) Blood 93, 2707-20.
    16. Kabarowski, J.H. and Witte, O.N. (2000) Stem Cells 18, 399-408.
    For Research Use Only. Not For Use In Diagnostic Procedures.
    Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
    PathScan is a registered trademark of Cell Signaling Technology, Inc.
    All other trademarks are the property of their respective owners. Visit our Trademark Information page.