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    Ginsenoside Rd2 (Quinquenoside L10)
    Ginsenoside Rd2 (Quinquenoside L10)
    Information
    CAS No. 83480-64-2 Price $318 / 10mg
    Catalog No.CFN95231Purity>=98%
    Molecular Weight917.2Type of CompoundTriterpenoids
    FormulaC47H80O17Physical 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 / $318 / In-stock
    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: Reference standards.
    Ginsenoside Rd2 (Quinquenoside L10) Description
    Source: The roots of Panax ginseng C. A. Mey.
    Solvent: DMSO, Pyridine, Methanol, Ethanol, 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 1.0903 mL 5.4514 mL 10.9027 mL 21.8055 mL 27.2569 mL
    5 mM 0.2181 mL 1.0903 mL 2.1805 mL 4.3611 mL 5.4514 mL
    10 mM 0.109 mL 0.5451 mL 1.0903 mL 2.1805 mL 2.7257 mL
    50 mM 0.0218 mL 0.109 mL 0.2181 mL 0.4361 mL 0.5451 mL
    100 mM 0.0109 mL 0.0545 mL 0.109 mL 0.2181 mL 0.2726 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:
    Modern chinese medicine, 2018.
    Saponin Constituents from Fruits of Panax ginseng.[Reference: WebLink]
    To study the saponin constituents of in the fruits of Panax ginseng C. A. Meyer.
    METHODS AND RESULTS:
    The chemical constituents were isolated and purified by various chromatographic methods including macroporous resin,MCI gel, silica gel columns and semi-preparative HPLC, and their structures were identified by NMR and MS data analysis. Twenty-two compounds were isolated and identified as ginsenoside F2(1),vina-ginsenoside R8(2),pseudoginsenoside Rc1(3),ginsenoside Re(4),notoginsenoside R2(5),ginsenoside F5(6),ginsenoside F3(7),ginsenoside Ia(8),chikusetsusaponin LM1(9),20(S)-ginsenoside Rg2(10),ginsenoside Rc(11),ginsenoside F1(12),ginsenoside Rd(13),ginsenoside Rb2(14),ginsenoside Rb1(15),ginsenoside Rh6(16),ginsenoside Rh4(17),ginsenoside Rh5(18),gypenoside XⅦ(19),gypenoside IX(20),notoginsenoside Fe(21) and Ginsenoside Rd2 (Quinquenoside L10)(22).
    CONCLUSIONS:
    Compounds 2,3,5,8,9,16,18-22 were isolated from the fruits of P. ginseng for the first time.
    Journal of Asian Natural Products Research, 2009, 11(3):195-201.
    Three new triterpenoid saponins from the leaves and stems of Panax quinquefolium.[Reference: WebLink]
    Three new minor dammarane saponins, Ginsenoside Rd2 (Quinquenoside L10) (1), L14 (2), and L16 (3), were isolated from the leaves and stems of Panax quinquefolium L.
    METHODS AND RESULTS:
    By the combination of one- and two-dimensional NMR techniques and MS spectroscopic analysis, their structures were established as 20-O-(alpha-L-arabinopyranosyl-(1-6)-O-beta-D-glucopyranosyl)-3-O-beta-D-glucopyranosyl-dammar-24-ene-3,12, 20-triol (1), 20-O-alpha-L-arabinopyranosyl-3-O-(beta-D-glucopyranosyl-(1-2)-O-beta-d-glucopyranosyl)-dammar-24-ene-3,12,20-triol (2), 3-O-(beta-D-glucopyranosyl-(1-2)-O-beta-d-glucopyranosyl)-20-O-(beta-D-glucopyranosyl-(1-6)-beta-D-glucopyranosyl)-dammarane-3,12,20,24,25-pentaol (3).
    CONCLUSIONS:
    The content of artemisinin was significantly enhanced by 3.0 mg l(- 1) of compounds 1, 2, and 3 in the callus of Artemisia annua.