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    Ganoderic acid L
    Information
    CAS No. 102607-24-9 Price $413 / 5mg
    Catalog No.CFN95022Purity>95%
    Molecular Weight534.7Type of CompoundAlkaloids
    FormulaC30H46O8Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)
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    According to end customer requirements, ChemFaces provide solvent format. This solvent format of product intended use: Signaling Inhibitors, Biological activities or Pharmacological activities.
    Size /Price /Stock 10 mM * 1 mL in DMSO / $883.3 / In-stock
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    Description: Ganoderic acid L is a natural product from the fruiting body of the fungus Ganoderma lucidum (Reishi).
    Ganoderic acid L 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.
    IF=36.216(2019)

    PMID: 29328914

    Cell Metab. 2020 Mar 3;31(3):534-548.e5.
    doi: 10.1016/j.cmet.2020.01.002.
    IF=22.415(2019)

    PMID: 32004475

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.
    IF=14.548(2019)

    PMID: 29149595

    ACS Nano. 2018 Apr 24;12(4): 3385-3396.
    doi: 10.1021/acsnano.7b08969.
    IF=13.903(2019)

    PMID: 29553709

    Nature Plants. 2016 Dec 22;3: 16206.
    doi: 10.1038/nplants.2016.205.
    IF=13.297(2019)

    PMID: 28005066

    Sci Adv. 2018 Oct 24;4(10): eaat6994.
    doi: 10.1126/sciadv.aat6994.
    IF=12.804(2019)

    PMID: 30417089
    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.8702 mL 9.351 mL 18.7021 mL 37.4042 mL 46.7552 mL
    5 mM 0.374 mL 1.8702 mL 3.7404 mL 7.4808 mL 9.351 mL
    10 mM 0.187 mL 0.9351 mL 1.8702 mL 3.7404 mL 4.6755 mL
    50 mM 0.0374 mL 0.187 mL 0.374 mL 0.7481 mL 0.9351 mL
    100 mM 0.0187 mL 0.0935 mL 0.187 mL 0.374 mL 0.4676 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:
    Journal of the Agricultural Chemical Society of Japan, 1986, 50(3):809-811.
    New Terpenoids, Ganolucidic Acid D, Ganoderic Acid L, Lucidone C and Lucidenic Acid G, from the Fungus Ganoderma lucidum.[Reference: WebLink]
    The fruiting body of the fungus Ganoderma lucidum (Reishi) has attracted much attention as a folk medicine, and some of its components have been elucidated.
    METHODS AND RESULTS:
    We have also reported several bitter terpenoids and related compounds from the fungus.1~9) The naming of lucidenic acids is a little confused, so we now designate our lucidenic acids D and E2) as Dx and El5 and Kikuchi's7) as D2 and E2, respectively. Recently, we have isolated four new terpenoids, ganolucidic acid D (1), methyl ganoderate L (2a), lucidone C (3) and methyl lucidenate G (4a). Ganolucidic acid D (1) has a allylic alcohol group in the side chain and can the mycelial components10) and terpenoids of the fruiting body. On the other hand, Ganoderic acid L (2), which has a hydroxyl group at C-20, can be a possible precursor of lucidone C (3).
    CONCLUSIONS:
    Among the lucidenic acids, lucidenic acid G (4) is unique in having a hydroxyl group at C-26.