Carnosic acid

SKU:BHB11900150
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    Overview
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    Carnosic acid is a research-grade small-molecule activator of PPARγ for Cancer and Apoptosis studies. Supplied as a off white to yellow solid with 95% purity (CAS 3650-09-7, MW 332.43) soluble in DMSO; store at -20°C. For research use only.
    Cas No. 3650-09-7
    Molecular Formula C20H28O4
    Purity ≥95% (HPLC); NMR(Conforms)
    Application Notes PPARγ activator
    Available Options

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

    • Options: Size (2) — 10 mg, 50 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-362-10MG 10 mg
    SIH-362-50MG 50 mg
    Field Specification
    Activity
    • Activator
    Alternative Names (4aR,10aS)-5,6-Dihydroxy-7-isopropyl-1,1-dimethyl-1,3,4,9,10,10a-hexahydro-2H-phenanthrene-4a-carboxylic acid
    Cas No. 3650-09-7
    Form Off white to yellow solid
    Molecular Weight 332.43
    Product Type
    • Biochemicals
    • Small Molecules
    Purity ≥95% (HPLC); NMR(Conforms)
    Shipping Shipped Ambient
    SMILES CC(C)C1=C(C(=C2C(=C1)CC[C@@H]3[C@@]2(CCCC3(C)C)C(=O)O)O)O
    Solubility Soluble in DMSO (50 mg/ml)
    Source Synthetic
    Storage -20ºC

    Carnosic acid is a phenolic diterpene found in rosemary and sage, known for its potent antioxidant and neuroprotective properties. In neuroscience, carnosic acid has gained attention for its ability to activate the Nrf2-ARE pathway, a critical regulator of cellular defense against oxidative stress. This activation leads to the upregulation of detoxifying and antioxidant enzymes, offering protection against neuronal damage in models of Alzheimer’s, Parkinson’s, and ischemic stroke. Carnosic acid also exhibits anti-inflammatory effects by modulating microglial activation and cytokine production. Its dual action on oxidative stress and inflammation makes it a promising candidate for therapeutic development in neurodegenerative disease research.

    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

    Carnosic acid (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-362)

    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. Schwarz K., Ternes W. (1992) Zeitschrift für Lebensmittel-Untersuchung und –Forschung. 195 (2): 99-103.
    2. Chen J.H., et al. Chem. (2012) Res. Toxicol 25:1893.
    3. Takahashi T., et al. (2009) Biochem. Biophys. Res. Commun. 382:549.
    4. Kar S., et al. (2012) Apoptosis. 17:1735.
    5. Barni M.V., et al. (2012) Oncol. Rep. 27:1041.

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