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    Natural Products
    Soyacerebroside II
    Information
    CAS No. 115074-93-6 Price
    Catalog No.CFN99250Purity>=98%
    Molecular Weight714.0 Type of CompoundCerebrosides
    FormulaC40H75NO9Physical DescriptionPowder
    Download Manual    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
    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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    Soyacerebroside II

    Soyacerebroside II
    Product Name Soyacerebroside II
    CAS No.: 115074-93-6
    Catalog No.: CFN99250
    Molecular Formula: C40H75NO9
    Molecular Weight: 714.0 g/mol
    Purity: >=98%
    Type of Compound: Cerebrosides
    Physical Desc.: Powder
    Targets: IL Receptor | Calcium Channel
    Source: The fruits of Glycine max
    Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
    Price:
    Inquire / Order: manager@chemfaces.com
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  • J Mol Med (Berl).2018, 96(7):661-672
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  • Journal of Third Military Medical University2019, 41(2):110-115
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  • Related Screening Libraries
    Size /Price /Stock 10 mM * 100 uL in DMSO / Inquiry / In-stock
    10 mM * 1 mL in DMSO / Inquiry / In-stock
    Related Libraries
  • Immunomodulators Compound Library
  • Cerebrosides Compound Library
  • IL Receptor Inhibitor Library
  • Calcium Channel Inhibitor Library
  • Biological Activity
    Description: Soyacerebroside II exhibits ionophoretic activity for Ca2+ ion. Soyacerebrosides I and II have modulating the cellular immune response effects, they show obvious inhibitory activity on IL-18 secretion in human peripheral blood mononuclear cells (PBMC).
    Targets: IL Receptor | Calcium Channel
    In vitro:
    Chem Pharm Bull (Tokyo). 1990 Nov;38(11):2933-8.
    Sphingolipids and glycerolipids. I. Chemical structures and ionophoretic activities of soya-cerebrosides I and II from soybean.[Pubmed: 2085876]

    METHODS AND RESULTS:
    Two glycosphingolipids named soya-cerebrosides I and II were isolated from soybean, the seeds of Glycine max Merrill (Leguminosae), and their chemical structures have been elucidated on the basis of physicochemical evidence and several chemical degradation reactions.
    CONCLUSIONS:
    By using a newly constructed liquid membrane-type apparatus (W-08) for measurement of ion-transport and ion-binding activities and by employing a method using human erythrocyte membranes for measurement of ion-permeability, it has been found that Soyacerebroside II exhibits ionophoretic activity for Ca2+ ion.
    Lipids. 2009 Aug;44(8):759-63.
    An isomeric mixture of novel cerebrosides isolated from Impatiens pritzellii reduces lipopolysaccharide-induced release of IL-18 from human peripheral blood mononuclear cells.[Pubmed: 19609788]
    An isomeric mixture of two cerebrosides, soyacerebroside I and Soyacerebroside II, was isolated from an ethno drug, the rhizomes of Impatiens pritzellii Hook. f. var. hupehensis Hook. f., and their structures were identified by spectroscopic (NMR, MS) analysis.
    METHODS AND RESULTS:
    In order to determine the immunomodulatory activities of soya-cerebrosides I and II, the effects of the mixture of cerebrosides (MC) on cytotoxicity of human peripheral blood mononuclear cells (PBMC) and the inhibitory activities to lipopolysaccharide (LPS)-induced interleukin (IL)-18 in PBMC were studied. The MC at concentrations of 10 and 1 microM, without toxicity to PBMC in 24 h, showed obvious inhibitory activity on IL-18 secretion.
    CONCLUSIONS:
    Because of this effect of modulating the cellular immune response, soya-cerebrosides I and II were considered to be the active substances of this ethno drug.
    Soyacerebroside II Description
    Source: The fruits of Glycine max
    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 1.4006 mL 7.0028 mL 14.0056 mL 28.0112 mL 35.014 mL
    5 mM 0.2801 mL 1.4006 mL 2.8011 mL 5.6022 mL 7.0028 mL
    10 mM 0.1401 mL 0.7003 mL 1.4006 mL 2.8011 mL 3.5014 mL
    50 mM 0.028 mL 0.1401 mL 0.2801 mL 0.5602 mL 0.7003 mL
    100 mM 0.014 mL 0.07 mL 0.1401 mL 0.2801 mL 0.3501 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:
    Zhongguo Zhong Yao Za Zhi. 2014 Jan;39(2):258-61.
    Chemical constituents from leaves of Ilex latifolia.[Pubmed: 24761642]

    METHODS AND RESULTS:
    Nine compounds were isolated from the leaves of Ilex latifolia. Their structures were respectively identified as 5-hydroxy-6, 7, 8, 4'-tetramethoxyflavone (1), tangeretin (2), nobiletin (3), 5-hydroxy-6, 7, 8, 3', 4'-pentamethoxyflavone (4), 5, 6, 7, 8, 4'-pentamethoxyflavonol (5), 5, 6, 7, 8, 3', 4'-hexamethoxy-flavonol (6), 5-hydroxy-3', 4', 7-trimethoxyflavanone (7), soyacerebroside I (8), and Soyacerebroside II (9) by their physicochemical properties and spectroscopic data.
    CONCLUSIONS:
    Compounds 1-9 were isolated from this plant for the first time.
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