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Medchemexpress LLC GSK-J4 | 1373423-53-0 | 99.45% | 417.50 | 50 MG
SDP

Catalog No. 5000364267
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GSK-J4 is a potent dual inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A, with IC50s of 8.6 μM and 6.6 μM respectively. This cell-permeable proagent of GSK-J1 induces endoplasmic reticulum stress-related apoptosis and inhibits LPS-induced TNF-α production in human primary macrophages.

  • Potent dual inhibitor of H3K27me3/me2-demethylases
  • Inhibits LPS-induced TNF-α production in human primary macrophages
  • Cell-permeable proagent
  • Induces endoplasmic reticulum stress-related apoptosis
  • Increases total nuclear H3K27me3 levels in untransfected cells
  • Reduces Jagged-1 mRNA and protein levels
  • Promotes differentiation of Treg cells

Catalog No. 50-003-64267 Supplier Medchemexpress LLC Supplier No. 50MGHY15648B
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GSK-J4 is a potent dual inhibitor of H3K27me3/me2-demethylases JMJD3/KDM6B and UTX/KDM6A, with IC50s of 8.6 μM and 6.6 μM respectively. This cell-permeable proagent of GSK-J1 induces endoplasmic reticulum stress-related apoptosis and inhibits LPS-induced TNF-α production in human primary macrophages.

  • Potent dual inhibitor of H3K27me3/me2-demethylases
  • Inhibits LPS-induced TNF-α production in human primary macrophages
  • Cell-permeable proagent
  • Induces endoplasmic reticulum stress-related apoptosis
  • Increases total nuclear H3K27me3 levels in untransfected cells
  • Reduces Jagged-1 mRNA and protein levels
  • Promotes differentiation of Treg cells

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