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    Acerogenin G
    Acerogenin G
    Information
    CAS No. 130233-83-9 Price
    Catalog No.CFN89027Purity>=98%
    Molecular Weight298.38Type of CompoundPhenols
    FormulaC19H22O3Physical DescriptionOil
    Download     COA    MSDSSimilar structuralComparison
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    Size /Price /Stock 10 mM * 1 mL in DMSO / Inquiry
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    Description: Acerogenin G is a natural product from Acer nikoense.
    Acerogenin G Description
    Source: The stem barks of Acer nikoense
    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 3.3514 mL 16.7572 mL 33.5143 mL 67.0286 mL 83.7858 mL
    5 mM 0.6703 mL 3.3514 mL 6.7029 mL 13.4057 mL 16.7572 mL
    10 mM 0.3351 mL 1.6757 mL 3.3514 mL 6.7029 mL 8.3786 mL
    50 mM 0.067 mL 0.3351 mL 0.6703 mL 1.3406 mL 1.6757 mL
    100 mM 0.0335 mL 0.1676 mL 0.3351 mL 0.6703 mL 0.8379 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:
    Tetrahedron, 2013, 69(13):2807-2815.
    Total synthesis of acerogenins E, G and K, and centrolobol.[Reference: WebLink]

    METHODS AND RESULTS:
    The first total synthesis of the diarylheptanoid acerogenins E and K, isolated from Acer nikoense MAXIM., is described. Formation of the 13-membered m,m-cyclophane skeleton was successfully achieved on the basis of a domino process involving a Miyaura arylborylation–intramolecular Suzuki reaction. The cyclization precursor was prepared via a Wittig reaction and Claisen–Schmidt condensation, which proceeded in moderate yields.
    CONCLUSIONS:
    The total synthesis of Acerogenin G and centrolobol was also achieved from a common synthetic intermediate.