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    6,8-Diprenylnaringenin
    Information
    CAS No. 68236-11-3 Price
    Catalog No.CFN92018Purity>=98%
    Molecular Weight408.5Type of CompoundFlavonoids
    FormulaC25H28O5Physical DescriptionCryst.
    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 / Inquiry
    Other Packaging *Packaging according to customer requirements(100uL/well, 200uL/well and more), and Container use Storage Tube With Screw Cap
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    Description: 6,8-Diprenylnaringenin is a natural product from Humulus lupulus.
    6,8-Diprenylnaringenin Description
    Source: The herbs of Humulus lupulus
    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 2.448 mL 12.2399 mL 24.4798 mL 48.9596 mL 61.1995 mL
    5 mM 0.4896 mL 2.448 mL 4.896 mL 9.7919 mL 12.2399 mL
    10 mM 0.2448 mL 1.224 mL 2.448 mL 4.896 mL 6.12 mL
    50 mM 0.049 mL 0.2448 mL 0.4896 mL 0.9792 mL 1.224 mL
    100 mM 0.0245 mL 0.1224 mL 0.2448 mL 0.4896 mL 0.612 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:
    Chemical & Pharmaceutical Bulletin , 2008 , 36 (9) :3292-3295.
    A new flavonoid and other new components from Citrus plants.[Reference: WebLink]

    METHODS AND RESULTS:
    A new flavonoid, citflavanone (1), and prenylated phenol derivatives, etrogol (7) and valencic acid (8), were isolated from roots and root barks of Citrus natsudaidai (natsudaidai), C. medica (etrog citron), C. sinensis (valencia orange), and several hybrid seedlings resulting from hyuga-natsu × hirakishu, and characterized. In order to determine the structure of citflavanone (1), prenylation of naringenin (3) was attempted to give 6- and 8-prenylnaringenin (4 and 5,respectively) as well as 6,8-Diprenylnaringenin (6).
    CONCLUSIONS:
    The location of the prenyl moiety in 4 and 5 was established by means of the long-range selective proton decoupling technique in nuclear magnetic resonance spectrometry.