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    Myristicin molecular structure

    Myristicin Stats & Data

    PubChem
    MW192.21
    FormulaC11H12O3
    LogP2.9
    IUPAC4-methoxy-6-prop-2-enyl-1,3-benzodioxole
    InChIKeyBNWJOHGLIBDBOB-UHFFFAOYSA-N
    Chemical Class Cannabinoid

    Pharmacology

    DrugBank

    Mechanism of Action

    To evaluate the hepatoprotective activity of spices, 21 different spices were fed to rats with liver damage caused by lipopolysaccharide (LPS) plus d-galactosamine (D-GalN). As assessed by plasma aminotranferase activities, nutmeg showed the most potent hepatoprotective activity. Bioassay-guided isolation of the active compound from nutmeg was carried out in mice by a single oral administration of the respective fractions. Myristicin, one of the major essential oils of nutmeg, was found to posse

    Metabolism

    In mice, the major metabolic pathway for ... myristicin includes cleavage of the methylenedioxyphenol residue and exhalation of the methylene carbon atom as carbon dioxide.

    Toxicity

    PubChem

    Myristicin exerts possible neurotoxic effects on dopaminergic neurons and is a weak inhibitor of monoamine oxidase. (L1271)

    LD50

    • LD50: 3000 mg/kg (Oral, Mouse) (L1272)
    • LD50: 340 mg/kg (Intraperitoneal, Mouse) (L1272)
    • LD50: 5610 mg/kg (Dermal, Rat) (L1272)
    • LD50: 1470 mg/kg (Subcutaneous, Mouse) (L1272)
    • LD50: 8000 mg/kg (Intramuscular, Mouse) (L1272)

    Carcinogenicity

    No indication of carcinogenicity to humans (not listed by IARC).

    Health effects (PubChem excerpts)

    Myristicin has neurotoxic effects and hallucinogenic properties. (L1271)

    Tolerance & Pharmacokinetics

    drugs.wiki

    Tolerance Decay

    Full tolerance 3d Half tolerance 21d Baseline ~28d
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