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Biological Activities
✨ Anticancer in vitro 🔥 Anti-inflammatory in vitro 🦠 Antibacterial in vitro
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Home Natural Compounds 8,9-Dihydro-4,8-dimethylphenanthro(3,2-b)furan-7,11-dione
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2-Geranyl-4-isobutyrylphloroglucinol
2-Geranyl-4-isobutyrylphloroglucinol $1,207.50

8,9-Dihydro-4,8-dimethylphenanthro(3,2-b)furan-7,11-dione

$1,499.00

CAS Number: 20958-18-3

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PuritySizePriceStockQuantity
95%5mg$1,499.00In stock
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    SKU: ACU040005 Category: Natural Compounds
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    • Description
    • Additional information
    • Biological Activity
    • Natural Sources
    • Reviews (0)
    • ANSWERS TO EVERYTHING ELSE
    Description

    Anti-tumor; Anticancer; Danshen; Red root grass; Diterpenoid quinone; Herbology Reference; Herbology Standard; Plant extract; Natural products; Natural products library

    Additional information
    Size

    5mg

    Purity

    95%

    M.F.

    C18H14O3

    Appearance

    Red powder

    H NMR

    Available

    Biological Activity

    Reported Biological Activities

    Click each activity to expand detailed pharmacology data.

    ✨ Anticancer in vitro ED50 2.5 uM (thyroid cancer); IC50 1-20 uM (various)
    −
    IC50
    ED50 2.5 uM (thyroid cancer); IC50 1-20 uM (various)
    Potency
    High (4/5)
    Thyroid cancer ED50
    2.5 uM (beta-catenin down)
    HCC apoptosis
    30-40% at 5 uM
    Endometrial
    10 uM apoptosis+ferroptosis
    Glioblastoma
    STAT3 inhibitor
    Esophageal
    STAT3 + mitochondrial pathway
    Mechanism of Action
    Norditerpenoid quinone from Salvia miltiorrhiza; multi-pathway antitumor agent: inhibits STAT3 signaling (esophageal cancer, glioblastoma), downregulates beta-catenin (papillary thyroid cancer ED50 2.5 uM), induces DNA damage and EGFR pathway inhibition (hepatocellular carcinoma, 5 uM induces 30-40% apoptosis), triggers ferroptosis and apoptosis via GPX4 suppression (endometrial cancer, 10 uM), induces ER stress (prostate DU145), activates p38-mediated apoptosis (head and neck cancer); in vivo reduces tumor growth in xenograft models without obvious hepatotoxicity.
    References
    1. DHTS antitumor via beta-catenin downregulation in thyroid cancer. PMID: STAT3-mediated antitumor in esophageal SCC. PMC8371523
    🔥 Anti-inflammatory in vitro
    +
    Potency
    Medium (3/5)
    NF-kB
    inhibited
    TNF-alpha
    downregulated
    IL-6
    downregulated
    Mechanism of Action
    Tanshinone class compound; inhibits NF-kB activation and downregulates inflammatory cytokines (TNF-alpha, IL-6); quinone structure enables redox cycling and ROS generation which modulates inflammatory signaling; lipid-soluble component of Danshen used in cardiovascular and inflammatory conditions.
    References
    1. Tanshinones: anti-inflammatory via NF-kB inhibition. Salvia miltiorrhiza pharmacology review.
    🦠 Antibacterial in vitro
    +
    Potency
    Low (2/5)
    S. aureus
    inhibited
    Mechanism of Action
    Tanshinone class compound; shows antibacterial activity against Staphylococcus aureus; quinone structure may interfere with bacterial electron transport; lipid-soluble tanshinones contribute to Danshen antimicrobial properties.
    References
    1. Tanshinones antibacterial activity from Salvia miltiorrhiza.
    ⚠️ These biological activity data are for research reference only. Products are reagents for research use only and are not intended for human use.
    Natural Sources

    Natural Sources

    This compound can be found in the following natural sources. Each source is categorized by type.

    🌿
    Plant
    Salvia miltiorrhiza
    Danshen / Chinese sage. Dihydrotanshinone I is a major lipid-soluble tanshinone in roots; extracted by 95% ethanol reflux, water precipitation, ethyl acetate/petroleum ether extraction, silica gel column chromatography; often co-occurs with tanshinone IIA, tanshinone I, cryptotanshinone; used in cardiovascular disease and ischemic stroke.
    Source Categories: 🌿 Plant 🦠 Microbe 🐛 Animal 🌊 Marine
    Source information is for research reference only. Products are reagents for research use only and are not intended for human use.
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