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Render Timestamp: 2024-11-21T13:40:00.260Z
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XML generation date: 2024-04-24 09:10:49.157
Product last modified at: 2024-09-23T14:30:09.970Z
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PDP - Template Name: Chemical Modulators
PDP - Template ID: *******c501c72

Santacruzamate A (CAY10683) #69552

    Product Information

    Product Usage Information

    Santacruzamate A (CAY10683) is supplied as a lyophilized powder. For a 15 mM stock, reconstitute 5 mg of powder in 1.19 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 2 months to prevent loss of potency. Aliquot to avoid multiple freeze/thaw cycles.

    Product Description

    Molecular Weight 278.4 g/mol
    Purity >98%
    Molecular Formula C15H22N2O3
    CAS 1477949-42-0
    Solubility Soluble in DMSO at 25 mg/ml or ethanol at 20 mg/ml.

    Background

    Santacruzamate A (CAY10683) is a cytotoxin isolated from the Panamanian marine cyanobacterium cf. Symploca sp., and is a highly selective inhibitor of histone deacetylases (HDACs), specifically HDAC2 (IC50 = 0.119 nM) and HDAC6 (IC50 = 434 nM) (1). This small molecule has been shown to induce apoptosis via transcriptional inhibition of HDAC2, resulting in an increase of p21 Waf1/Cip1 and p19INK4d expression when combined with an HDAC1 inhibitor (2). Santacruzamate A (CAY10683) has also demonstrated the ability to attenuate amyloid-β protein (Aβ) fragment (Aβ25-35)-induced toxicity through enhancing endoplasmic reticulum (ER) stress tolerance in mice (3). Additionally, HDAC2 has been recognized as a host immune response to the influenza A virus (IVA) and several other viruses, making HDAC inhibitors important compounds to study in relation to viral diseases (4,5).
    For Research Use Only. Not For Use In Diagnostic Procedures.
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