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Render Timestamp: 2024-12-19T20:42:24.565Z
Commit: f2d32940205a64f990b886d724ccee2c9935daff
XML generation date: 2024-04-24 09:10:49.233
Product last modified at: 2024-12-17T18:59:15.293Z
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PDP - Template Name: Chemical Modulators
PDP - Template ID: *******c501c72

RIPA-56 #67765

    Product Information

    Product Usage Information

    RIPA-56 is supplied as a lyophilized powder. For a 20 mM stock, reconstitute 5 mg of powder in 1.13 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 221.3 g/mol
    Purity >98%
    Molecular Formula C13H19NO2
    CAS 1956370-21-0
    Solubility Soluble in DMSO at 50 mg/ml or ethanol at 50 mg/ml.

    Background

    RIPA-56 is a potent, selective, and metabolically stable inhibitor of receptor-interacting protein 1 (RIP1) kinase with an IC50 value of 13 nM, with no effect on RIP3 kinase activity at a 10 μM concentration. RIPA-56 has been shown to reduce TNFα-induced mortality and multiorgan damage in systemic inflammatory response syndrome (SIRS) (1). Blocking the activity of RIP1 kinase allows for cell survival and proliferation in the presence of death receptor ligands. In vivo studies have also shown that necroptosis can be inhibited in the testes of busulfan-induced mice by the suppression of RIP1 kinase with RIPA-56 (2). This small molecule can protect myelin structures by blocking the demyelination and inflammation of spinal cord white matter in mice experimental autoimmune encephalomyelitis (EAE)-induced models, halting the progression of multiple sclerosis (MS) (3).
    For Research Use Only. Not For Use In Diagnostic Procedures.
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