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Chemical Structure
Chemical Structure
Chemical Structure

PD 98,059 [167869-21-8]

Research Use Only
AG-CR1-0118
AdipoGen Life Sciences
CAS Number167869-21-8
Product group Chemicals
Estimated Purity>98%
Molecular Weight267.3
Price on request
Packing Size
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    PD 98,059 [167869-21-8]
  • Delivery Days Customer
    10
  • CAS Number
    167869-21-8
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Hazard Information
    Warning
  • Molecular Formula
    C16H13NO3
  • Molecular Weight
    267.3
  • Scientific Description
    Chemical. CAS: 167869-21-8. Formula: C16H13NO3. MW: 267.3. Highly selective, reversible and cell permeable MEK (MAP kinase kinase) inhibitor. Blocks the phosphorylation and activation of the MAP kinase pathway. T cell activation inhibitor. Inhibits cell growth and cell proliferation of several cancer cells. - Highly selective, reversible and cell permeable MEK (MAP kinase kinase) inhibitor [1-3, 7]. Blocks the phosphorylation and activation of the MAP kinase pathway [1-3, 7]. T cell activation inhibitor [4]. Inhibits cell growth and cell proliferation of several cancer cells [5, 6, 8].
  • SMILES
    COC1=C(N)C(=CC=C1)C1=CC(=O)C2=CC=CC=C2O1
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352200

References

  • A synthetic inhibitor of the mitogen-activated protein kinase cascade: D.T. Dudley, et al.; PNAS 92, 7686 (1995)
  • Inhibition of MAP kinase kinase blocks the differentiation of PC-12 cells induced by nerve growth factor: L. Pang, et al.; J. Biol. Chem. 270, 13585 (1995)
  • PD 098059 is a specific inhibitor of the activation of mitogen-activated protein kinase kinase in vitro and in vivo: D. Alessi, et al.; J. Biol. Chem. 270, 27489 (1995)
  • Inhibition of T cell activation by pharmacologic disruption of the MEK1/ERK MAP kinase or calcineurin signaling pathways results in differential modulation of cytokine production: F.J. Dumont, et al.; J. Immunol. 160, 2579 (1998)
  • A phosphatidylinositol 3-kinase inhibitor induces a senescent-like growth arrest in human diploid fibroblasts: M. Tresini, et al.; Cancer Res. 58, 1 (1998)
  • PD 098059, an inhibitor of ERK1 activation, attenuates the in vivo invasiveness of head and neck squamous cell carcinoma: C. Simon, et al.; Br. J. Cancer 80, 1412 (1999)
  • Specificity and mechanism of action of some commonly used protein kinase inhibitors. S.P. Davies, et al.; Biochem. J. 351, 95 (2000)
  • Mitogen-activated protein kinase kinase inhibition enhances nuclear proapoptotic function of p53 in acute myelogenous leukemia cells: K. Kojima, et al.; Cancer Res. 67, 3210 (2007)