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    Natural Products
    Acanthopanaxoside B
    Acanthopanaxoside B
    Information
    CAS No. 915792-03-9 Price
    Catalog No.CFN93301Purity>=98%
    Molecular Weight1263.43Type of CompoundTriterpenoids
    FormulaC61H98O27Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)  (SDF)
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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
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    Acanthopanaxoside B

    Acanthopanaxoside B
    Product Name Acanthopanaxoside B
    CAS No.: 915792-03-9
    Catalog No.: CFN93301
    Molecular Formula: C61H98O27
    Molecular Weight: 1263.43 g/mol
    Purity: >=98%
    Type of Compound: Triterpenoids
    Physical Desc.: Powder
    Source: The herbs of Acanthopanax senticosus
    Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
    Price:
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    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
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    Description: Reference standards.
    Acanthopanaxoside B Description
    Source: The herbs of Acanthopanax senticosus
    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 0.7915 mL 3.9575 mL 7.915 mL 15.8299 mL 19.7874 mL
    5 mM 0.1583 mL 0.7915 mL 1.583 mL 3.166 mL 3.9575 mL
    10 mM 0.0791 mL 0.3957 mL 0.7915 mL 1.583 mL 1.9787 mL
    50 mM 0.0158 mL 0.0791 mL 0.1583 mL 0.3166 mL 0.3957 mL
    100 mM 0.0079 mL 0.0396 mL 0.0791 mL 0.1583 mL 0.1979 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:
    J Nat Prod. 2006 Nov;69(11):1577-81.
    Biologically active triterpenoid saponins from Acanthopanax senticosus.[Pubmed: 17125224 ]

    METHODS AND RESULTS:
    Three new triterpenoid saponins, acanthopanaxoside A (1), Acanthopanaxoside B (7), and acanthopanaxoside C (13), were isolated from the leaves of Acanthopanax senticosus, together with 12 known saponins. The structures of these new saponins were established as 3-O-beta-D-glucopyranosyl-(1-->2)-alpha-L-arabinopyranosyl-30-nor-olean-12,20(29)-dien-28-oic acid 28-O-alpha-L-rhamnopyranosyl-(1-->4)-6-O-acetyl-beta-D-glucopyranosyl-(1-->6)-beta-D-glucopyranosyl ester (1), 3-O-beta-D-glucopyranosyl-(1-->2)-alpha-L-arabinopyranosyl oleanolic acid 28-O-alpha-L-rhamnopyranosyl-(1-->4)-6-O-acetyl-beta-D-glucopyranosyl-(1-->6)-beta-D-glucopyranosyl ester (7), and 3-O-alpha-L-rhamnopyranosyl-(1-->2)-alpha-L-arabinopyranosyl-3beta-hydroxyolean-12-ene-28,29-dioic acid (13), on the basis of spectroscopic analysis and chemical degradation. Among the known compounds, sessiloside and tauroside H1 are reported for the first time from A. senticosus.
    CONCLUSIONS:
    The biological activity of compounds 1-15 was examined against pancreatic lipase. Ciwujianoside C1 (6), tauroside H1 (11), 3-O-alpha-rhamnopyranosyl-(1-->2)-alpha-arabinopyranosyl mesembryanthemoidigenic acid (12), acanthopanaxoside C (13), sessiloside (14), and chiisanoside (15) inhibited pancreatic lipase activity in vitro. In turn, ciwujianosides C2 (3), D2 (5), C4 (8), and C3 (10) and hederasaponin B (9) enhanced this enzyme.
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