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Render Timestamp: 2024-10-25T10:55:38.388Z
Commit: 56767fe525c928647c8401233a175d0d607d385d
XML generation date: 2024-09-19 21:57:39.552
Product last modified at: 2024-09-30T19:15:07.544Z
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PDP - Template Name: Chemical Modulators
PDP - Template ID: *******c501c72

Trametinib #62206

    Product Information

    Product Usage Information

    Trametinib is supplied as a lyophilized powder. For a 15 mM stock, reconstitute 10 mg of powder in 1.08 ml of DMSO. Working concentrations and length of treatment can vary depending on the desired effect.

    Storage

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

    Product Description

    Molecular Weight 615.4 g/mol
    Purity >98%
    Molecular Formula C26H23FIN5O4
    CAS 871700-17-3
    Solubility Soluble in DMSO at 20 mg/ml with slight warming.

    Background

    Trametinib, also known as GSK1120212, is a potent and selective inhibitor of MEK with an IC50 of 0.7 nM for u-MEK1 and 14.9 nM for pp-MEK1 (1). When compared to several tyrosine kinase inhibitors (TKIs) and MEK inhibitors (MEKIs) in endothelial cells, Trametinib displays the highest level of antiangiogenic activity and is the most effective ERK1/2 inhibitor (IC50 = 1.3 nM) (2). Trametinib has also been shown to be the most effective at reducing proliferation in low-grade serous ovarian cancers (LGSCs) when compared to other MEKIs (3).
    For Research Use Only. Not For Use In Diagnostic Procedures.
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