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    Ethyl ganoderate J
    Information
    CAS No. 1189555-95-0 Price
    Catalog No.CFN92576Purity>=98%
    Molecular Weight542.7Type of CompoundTriterpenoids
    FormulaC32H46O7Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)
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    Biological Activity
    Description: Ethyl ganoderate J is a natural product from Ganoderma lucidum.
    Ethyl ganoderate J Description
    Source: The fruit body of Ganoderma lucidum
    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 1.8426 mL 9.2132 mL 18.4264 mL 36.8528 mL 46.066 mL
    5 mM 0.3685 mL 1.8426 mL 3.6853 mL 7.3706 mL 9.2132 mL
    10 mM 0.1843 mL 0.9213 mL 1.8426 mL 3.6853 mL 4.6066 mL
    50 mM 0.0369 mL 0.1843 mL 0.3685 mL 0.7371 mL 0.9213 mL
    100 mM 0.0184 mL 0.0921 mL 0.1843 mL 0.3685 mL 0.4607 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:
    Helvetica Chimica Acta.2009 Aug;92(8):1586–1593.
    Lanostanoids Isolated from Ganoderma lucidum Mycelium Cultured by Submerged Fermentation.[Reference: WebLink]

    METHODS AND RESULTS:
    Three new lanostane triterpene acids, 3-O-acetylganoderic acid B (1), 8β,9α-dihydroganoderic acid C (3), and 3-O-acetylganoderic acid K (4), as well as two new lanostane triterpene acid ethyl esters, ethyl 3-O-acetylganoderate B (2) and Ethyl ganoderate J (5), were isolated and characterized from Ganoderma lucidum mycelia which was cultured by submerged fermentation method. Their structures were elucidated on the basis of spectroscopic methods. In addition, the identification of two known lanostane triterpene acid methyl esters, methyl O-acetyl ganoderate C and methyl 3,7,11,15,23-pentaoxo-lanost-8-en-26-oate were identified by comparison of the NMR data with those reported in the literature.