Garcinol

SKU:BHB11900143
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    Overview
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    Garcinol is a research-grade small-molecule inhibitor of HAT for Cell Signaling and Epigenetics and Nuclear Signaling studies. Supplied as a yellow solid with >98% purity (CAS 78824-30-3, MW 602.8) soluble in 25 mg/ml DMSO or 25 mg/ml Ethanol; store at -20°C. For research use only.
    Cas No. 78824-30-3
    Molecular Formula C38H50O6
    Purity >98% (TLC), NMR conforms
    Application Notes HAT inhibitor
    Available Options

    Select the variant that best fits your experiment. Availability and lead time may vary by option.

    • Options: Size (2) — 25 mg, 5 mg.
    • Lead time: options listed as “in stock at manufacturer” typically ship in 2-3 business days; other statuses may take longer.
    • Storage: -20ºC
    • Shipping: ships at ambient temperature.
    • Upon receipt: store at the recommended temperature as soon as possible.
    • Sales terms and conditions: Please review prior to ordering.
    Options selector
    Catalog no. Size
    SIH-355-5MG 5 mg
    SIH-355-25MG 25 mg
    Field Specification
    Activity
    • Inhibitor
    Alternative Names Camboginol, 3-​(3,​4-​dihydroxybenzoyl)-​4-​hydroxy-​8,​8-​dimethyl-​1,​7-​bis(3-​methyl-​2-​buten-​1-​yl)-​5-​[(2S)-​5-​methyl-​2-​(1-​methylethenyl)-​4-​hexen-​1-​yl]-​bicyclo[3.3.1]non-​3-​ene-​2,​9-​dione
    Cas No. 78824-30-3
    Form Yellow solid
    Molecular Weight 602.8
    Product Type
    • Biochemicals
    • Small Molecules
    Purity >98% (TLC), NMR conforms
    Shipping Shipped Ambient
    SMILES CC(=CC[C@@H]1C[C@@]2(C(=C(C(=O)[C@@](C2=O)(C1(C)C)CC=C(C)C)C(=O)C3=CC(=C(C=C3)O)O)O)C[C@H](CC=C(C)C)C(=C)C)C
    Solubility Soluble in 25 mg/ml DMSO or 25 mg/ml Ethanol
    Source Synthetic
    Storage -20ºC

    Garcinol is a natural, cell-permeable inhibitor of histone acetyltransferases p300 and pCAF (IC₅₀ = 7 µM and 5 µM, respectively). It induces apoptosis, promotes hematopoietic stem cell expansion, and exhibits anti-inflammatory properties.

    In neuroscience, Garcinol has been shown to promote neurogenesis in cortical progenitor cells and suppress neuroinflammation in Alzheimer’s models by modulating NF-κB signaling. Its ability to regulate histone acetylation and transcriptional activity positions it as a promising compound for exploring epigenetic therapies in neurodegenerative diseases.

    Classification: Caution- Substance not yet fully tested.

    Safety Phrases:

    • S22 - Do not breathe dust
    • S36/37/39 - Wear suitable protective clothing, gloves and eye/face protection
    • S24/25- Avoid contact with skin and eyes

    Garcinol (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-355)

    Need this compound in a format that drops straight into your assay? We can tailor formulation, chemistry, and documentation so your results stay consistent across runs and re-orders.

    • Format options: solid or pre-dissolved solution (choose solvent), target concentration, aliquots, light/moisture-protected packaging
    • Chemistry options: free base/acid vs salt forms, hydrate/solvate preference, stereoisomer control (single enantiomer or racemate), close analogs
    • Add-on labels & handles: D/¹³C/¹⁵N isotopes (LC-MS/internal standards), azide/alkyne or other functional handles for conjugation
    • QC & documentation: standard COA or enhanced analytical pack (HPLC/LC-MS/NMR), chiral purity, residual solvents, water content (KF), method-specific specs
    • Scale & continuity: mg to gram scale, bulk pricing, lot reservation, repeat-order continuity

    To quote quickly, tell us: compound name + CAS/structure (SMILES or mol file), intended assay context, solvent preference, salt/stereochemistry requirements, purity/QC level, and the amount (mg–g).

    Can’t find the compound you’re looking for?
    Send the CAS or structure and your specs. We can help source it, suggest close equivalents, or discuss custom synthesis with the right QC documentation (RUO).

    1. Balasubramanyam K., et al., (2004) J. Biol. Chem. 279: 33716.
    2. Parasramka M.A., et al. (2011) Nutr. Cancer. 63: 456.
    3. Nishino T., et al. (2011) Nutr. PLoS One 6: e24298.

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