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    Eucannabinolide
    Eucannabinolide
    Information
    CAS No. 38458-58-1 Price
    Catalog No.CFN96916Purity>=98%
    Molecular Weight420.45Type of CompoundSesquiterpenoids
    FormulaC22H28O8Physical DescriptionOil
    Download     COA    MSDSSimilar structuralComparison (Web)
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    Biological Activity
    Description: Eucannabinolide exhibits in vivo antileukemic activity.
    Eucannabinolide Description
    Source: The roots and aerial parts of Eupatorium cannabium.
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Storage: Providing storage is as stated on the product vial and the vial is kept tightly sealed, the product can be stored for up to 24 months(2-8C).

    Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20C. Generally, these will be useable for up to two weeks. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.

    Need more advice on solubility, usage and handling? Please email to: service@chemfaces.com

    After receiving: The packaging of the product may have turned upside down during transportation, resulting in the natural compounds adhering to the neck or cap of the vial. take the vial out of its packaging and gently shake to let the compounds fall to the bottom of the vial. for liquid products, centrifuge at 200-500 RPM to gather the liquid at the bottom of the vial. try to avoid loss or contamination during handling.
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    Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.

    PMID: 29328914

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.

    PMID: 29149595

    Scientific Reports 2017 Dec 11;7(1):17332.
    doi: 10.1038/s41598-017-17427-6.

    PMID: 29230013

    Molecules. 2017 Oct 27;22(11). pii: E1829.
    doi: 10.3390/molecules22111829.

    PMID: 29077044

    J Cell Biochem. 2018 Feb;119(2):2231-2239.
    doi: 10.1002/jcb.26385.

    PMID: 28857247

    Phytomedicine. 2018 Feb 1;40:37-47.
    doi:10.1016/j.phymed.2017.12.030

    PMID: 29496173
    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.3784 mL 11.892 mL 23.784 mL 47.5681 mL 59.4601 mL
    5 mM 0.4757 mL 2.3784 mL 4.7568 mL 9.5136 mL 11.892 mL
    10 mM 0.2378 mL 1.1892 mL 2.3784 mL 4.7568 mL 5.946 mL
    50 mM 0.0476 mL 0.2378 mL 0.4757 mL 0.9514 mL 1.1892 mL
    100 mM 0.0238 mL 0.1189 mL 0.2378 mL 0.4757 mL 0.5946 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    Protocol
    Structure Identification:
    Phytochemistry, 1980, 19(6):1234-1237.
    Eucannabinolide and other constituents of Schkuhria virgata.[Reference: WebLink]
    Isolation of Eucannabinolide, its 3-isovaleroyl analog and pectolinarigenin from Schkuhria virgata (La Llave et Lex.) DC. is reported. The identity of Eucannabinolide, which exhibits in vivo antileukemic activity, with ‘hiyodorilactone A’, ‘20-hydroxychromolaenide’ and ‘schkuhrin I’ is discussed.
    Planta Med. 1987 Apr;53(2):169-72.
    Eupatoriopicrin 19-O-Linolenoate and Other Constituents from Eupatorium cannabium.[Pubmed: 17268990 ]
    The investigation of the roots and aerial parts of Eupatorium cannabium afforded, in addition to the sesquiterpene lactones eupatolide, eupatoriopicrin, and Eucannabinolide isolated previously, eight further lactones, three of which are new. Furthermore, in addition to known compounds, a new clerodane derivative and two further tremetone derivatives as well as 10-acetoxyneryl acetate were isolated.