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    Zingibroside R1
    Zingibroside R1
    Information
    CAS No. 80930-74-1 Price
    Catalog No.CFN92517Purity>=98%
    Molecular Weight795.0Type of CompoundTriterpenoids
    FormulaC42H66O14Physical DescriptionPowder
    Download Manual    COA    MSDS    SDFSimilar structuralComparison (Web)  (SDF)
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    * Packaging according to customer requirements(5mg, 10mg, 20mg and more). We shipped via FedEx, DHL, UPS, EMS and others courier.
    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
    Our products had been exported to the following research institutions and universities, And still growing.
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    Zingibroside R1

    Zingibroside R1
    Product Name Zingibroside R1
    CAS No.: 80930-74-1
    Catalog No.: CFN92517
    Molecular Formula: C42H66O14
    Molecular Weight: 795.0 g/mol
    Purity: >=98%
    Type of Compound: Triterpenoids
    Physical Desc.: Powder
    Targets: HIV
    Source: The roots of Achyranthes aspera
    Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
    Price:
    Inquire / Order: manager@chemfaces.com
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  • Molecules.2017, 22(11)
  • Analytical sci. & Tech2020, 33(5):224-231
  • J of Physics Conference Series2019, 1349(1)
  • Acta Agriculturae Scandinavica2015, 381-383
  • Bio-protocol2018, 9(14):e3301
  • Int J Mol Sci.2019, 21(1):E265
  • Biosci Biotechnol Biochem.2020, 84(3):621-632
  • Int J Food Sci Nutr.2019, 70(7):825-833
  • Clin Exp Pharmacol Physiol.2015, 42(11):1189-97
  • Am J Chin Med.2016, 44(8):1719-1735
  • Related Screening Libraries
    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
    10 mM * 1 mL in DMSO / Inquiry / In-stock
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  • Anticancer Compound Library
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  • Biological Activity
    Description: Zingibroside R1 has anti-HIV-1 activity.
    Targets: HIV
    In vitro:
    Planta Med. 1994 Jun;60(3):240-3.
    Inhibitory effect of some triterpenoid saponins on glucose transport in tumor cells and its application to in vitro cytotoxic and antiviral activities.[Pubmed: 8073091]

    METHODS AND RESULTS:
    The effects of some triterpenoid saponins on glucose transport in Ehrlich ascites tumor (EAT) cells were examined by measuring 2-deoxy-D-glucose (2-DG) uptake. The correlation of the effects with those on the growth of a human T-cell line (MT-4) and the replication of human immunodeficiency virus in MT-4 cells was also studied.
    CONCLUSIONS:
    Chikusetsusaponin Ia isolated from rhizomes of Panax japonicus C. A. Meyer (Araliaceae) inhibited the 2-DG uptake (IC50 = 76.3 microM) in a competitive fashion with respect to 2-DG (Ki = 0.32 mM) and the growth of MT-4 cells with CC50 of 84.4 microM, whereas it did not show any significant anti-HIV-1 activity. In contrast, Zingibroside R1 isolated from rhizomes of Panax zingiberensis Wu et Feng (Araliaceae) showed some anti-HIV-1 activity, which was found to be superior to that of glycyrrhizin, as well as the inhibitory effects on the 2-DG uptake by EAT cells (IC50 = 91.3 microM) and the growth of MT-4 cells (CC50 = 46.2 microM).
    Zingibroside R1 Description
    Source: The roots of Achyranthes aspera
    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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    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 1.2579 mL 6.2893 mL 12.5786 mL 25.1572 mL 31.4465 mL
    5 mM 0.2516 mL 1.2579 mL 2.5157 mL 5.0314 mL 6.2893 mL
    10 mM 0.1258 mL 0.6289 mL 1.2579 mL 2.5157 mL 3.1447 mL
    50 mM 0.0252 mL 0.1258 mL 0.2516 mL 0.5031 mL 0.6289 mL
    100 mM 0.0126 mL 0.0629 mL 0.1258 mL 0.2516 mL 0.3145 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:
    Chem Pharm Bull (Tokyo). 2013;61(3):344-50.
    Saponins composition of rhizomes, taproots, and lateral roots of Satsuma-ninjin (Panax japonicus).[Pubmed: 23291557]

    METHODS AND RESULTS:
    A new dammarane-type triterpenoid saponin, chikusetsusaponin VII (1), and nineteen known triterpenoid saponins, ginsenoside Rb1 (2), ginsenoside Rb3 (3), ginsenoside Rc (4), ginsenoside Rd (5), ginsenoside Re (6), ginsenoside Rg1 (7), ginsenoside Rg2 (8), ginsenoside Rh1 (9), notoginsenoside R1 (10), notoginsenoside R2 (11), notoginsenoside Fe (12), chikusetsusaponin IVa (13), chikusetsusaponin IV (14), chikusetsusaponin V (15), chikusetsusaponin VI (16), chikusetsusaponin FK6 (17), gypenoside XVII (18), 28-desglucosylchikusetsusaponin IV (19), and Zingibroside R1 (20), were isolated from rhizomes, taproots, and lateral roots of Panax japonicus C. A. Meyer, so-called "Satsuma-ninjin," grown in southern Miyazaki Prefecture, Japan. The structure of new chikusetsusaponin VII was elucidated on the basis of spectral and physicochemical evidence. Although the chemical composition of the rhizome was found to be similar to that of the "Chikusetsu-ninjin," the saponin composition of lateral root of "Satsuma-ninjin" was found to be close to that of lateral root of P. ginseng.
    CONCLUSIONS:
    The total yield of oleanolic acid saponins of the taproot was less than that of rhizome, but the total yield of dammarane-type saponins of the taproot was found to be similar to that of rhizome.
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