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Render Timestamp: 2025-01-23T18:38:34.808Z
Commit: da7e4f2f0d1aed1f1f8e20e4e2ecab8f33cbd595
XML generation date: 2024-09-20 06:23:30.907
Product last modified at: 2025-01-01T09:01:51.967Z
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PDP - Template Name: Chemical Modulators
PDP - Template ID: *******c501c72

PBIT #81379

    Product Information

    Product Usage Information

    PBIT is supplied as a lyophilized powder. For a 10 mM stock, reconstitute 1 mg of powder in 0.41 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 1 month to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

    Product Description

    Molecular Weight 241.3 g/mol
    Purity >98%
    Molecular Formula C14H11NOS
    CAS 2514-30-9
    Solubility Soluble in DMSO at 24 mg/mL or ethanol at 5 mg/mL.

    Background

    PBIT is a small-molecule inhibitor of lysine demethylase 5B (JARID1B or KDM5B), which demethylates Lys4 of histone H3. PBIT is also involved in cell fate decisions and is overexpressed in a variety of human cancers (1). PBIT inhibits JARID1B (IC50 of approximately 3 μM) and the related JARID1A and JARID1C demethylases less potently (IC50 of 6 and 4.9 μM, respectively). PBIT treatment of breast cancer cells increased lysine methylated histone H3 protein levels, suggesting that PBIT inhibits JARID1B demethylase in vivo (2). In a study of angiotensin II-induced endothelial dysfunction in mice, inhibition of JARID1B by PBIT reduced the inflammatory response and prevented the development of endothelial dysfunction (3). Overexpression of JARID1B in non-small cell lung cancer correlated with tumor size, lymph node metastasis, advanced stages, and poor overall survival; inhibition of JARID1B by PBIT enhanced cancer cell death and increased treatment effectiveness (4).
    For Research Use Only. Not For Use In Diagnostic Procedures.
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