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    Natural Products
    Gynosaponin I
    Gynosaponin I
    Information
    CAS No. 1207861-69-5 Price
    Catalog No.CFN96182Purity>=98%
    Molecular Weight769.0Type of CompoundTriterpenoids
    FormulaC42H72O12Physical DescriptionPowder
    Download     COA    MSDS    SDFSimilar 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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    Gynosaponin I

    Gynosaponin I
    Product Name Gynosaponin I
    CAS No.: 1207861-69-5
    Catalog No.: CFN96182
    Molecular Formula: C42H72O12
    Molecular Weight: 769.0 g/mol
    Purity: >=98%
    Type of Compound: Triterpenoids
    Physical Desc.: Powder
    Source: The herbs of Gynostemma pentaphyllum
    Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
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    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
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    Description: Gynosaponin I is a natural product from Gynostemma pentaphyllum.
    Gynosaponin I Description
    Source: The herbs of Gynostemma pentaphyllum
    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 1.3004 mL 6.502 mL 13.0039 mL 26.0078 mL 32.5098 mL
    5 mM 0.2601 mL 1.3004 mL 2.6008 mL 5.2016 mL 6.502 mL
    10 mM 0.13 mL 0.6502 mL 1.3004 mL 2.6008 mL 3.251 mL
    50 mM 0.026 mL 0.13 mL 0.2601 mL 0.5202 mL 0.6502 mL
    100 mM 0.013 mL 0.065 mL 0.13 mL 0.2601 mL 0.3251 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:
    Helvetica Chimica Acta, 2010 , 92 (12) :2737-2745.
    Six New Triterpenoid Glycosides from Gynostemma pentaphyllum.[Reference: WebLink]

    METHODS AND RESULTS:
    Six new triterpenoid glycosides, gynosaponins I–VI (Gynosaponin I , gynosaponin Ⅱ, gynosaponin Ⅲ, gynosaponin Ⅳ, gynosaponin Ⅴ, gynosaponin Ⅵ,1–6, resp.), together with three known compounds, ginseng Rb1 (7), gypenoside XLIX (8), and gylongiposide I (9), were isolated from the aerial parts of Gynostemma pentaphyllum.
    CONCLUSIONS:
    Based on ESI-MS, IR, 1D- and 2D-NMR data (HMQC, HMBC, COSY, and TOCSY), the structures of the new compounds were determined as (3β,12β,20S)-trihydroxydammar-24-ene 20-O-[α-rhamnopyranosyl-(1→2)]-β-glucopyranoside (1), (3β,12β,20S)-trihydroxydammar-24-ene 20-O-[α-rhamnopyranosyl-(1→2)] [α-rhamnopyranosyl-(1→3)]-β-glucopyranoside (2), (3β,12β,20S)-trihydroxydammar-24-ene 3-O-β-glucopyranosyl-20-O-[α-rhamnopyranosyl-(1→2)]-β-glucopyranoside (3), (3β,12β,20S)-trihydroxydammar-24-ene 3-O-β-glucopyranosyl-20-O-[α-rhamnopyranosyl-(1→2)] [α-rhamnopyranosyl-(1→3)]-β-glucopyranoside (4), (3β,12β,20S)-trihydroxydammar-24-ene 3-O-{[β-glucopyranosyl-(1→2)]-β-glucopyranosyl}-20-O-[α-rhamnopyranosyl-(1→2)]-β-glucopyranoside (5), and (3β,12β,20S)-trihydroxydammar-24-ene 3-O-{[β-glucopyranosyl-(1→2)]-β-glucopyranosyl}-20-O-[α-rhamnopyranosyl-(1→2)] [α-rhamnopyranosyl-(1→3)]-β-glucopyranoside (6).
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