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Category: Enzyme-Linked ReceptorsarrowReceptor Tyrosine Kinases (RTKs)arrowOther RTKs
Cat.No. Product Name
2086 GTP 14564
Price and Availability

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GTP 14564
Chemical Name: 3-Phenyl-1H-benzofuro[3,2-c]pyrazole

Biological Activity:

Potent, selective inhibitor of class III receptor tyrosine kinases (IC50 values are 0.3 μM for c-Fms, c-Kit, FLT3 and ITD-FLT3 and 1 μM for PDGFRβ). Displays no selectivity for ERK1, ERK2, EGFR, MEK1, HER2, Src, Abl, PKC, PKA and Akt (IC50 > 10 μM). Inhibits FL-dependent proliferation in BaF/ITD-FLT3 cells more potently than BaF/wt-FLT3 cells; anti-leukaemic.

Technical Data:

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M.Wt: 234.26
Formula: C15H10N2O
Storage: Store at +4°C
Solubility: Soluble to 100 mM in DMSO and to 25 mM in Ethanol
Purity: >99%
CAS No: [34823-86-4]

Resources:

  • Certificate of Analysis / MSDS:

    Certificate of Analysis is currently unavailable on-line. Please contact Customer Service
    Product/Material Safety Data Sheet: View current batch

    References:

    Murata et al (2003) Selective cytotoxic mechanism of GTP-14564, a novel tyrosine kinase inhibitor in leukemia cells expressing a constitutively active Fms-like tyrosine kinase 3 (FLT3). J.Biol.Chem. 278 32892. Yao et al (2005) Human leukemias with mutated FLT3 kinase are synergistically sensitive to FLT3 and Hsp90 inhibitors: the key role of the STAT5 signal transduction pathway. Leukemia 19 1605.
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    Keywords: GTP 14564, Receptor Tyrosine Kinases (RTKs), Class III Receptor Tyrosine Kinase (RTK) Inhibitor, GTP14564, Tocris Bioscience

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