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5'-Methoxylariciresinol
5'-Methoxylariciresinol
Information
CAS No. 105256-12-0 Price
Catalog No.CFN96706Purity>=98%
Molecular Weight390.43Type of CompoundLignans
FormulaC21H26O7Physical DescriptionPowder
Download COA    MSDSSimilar structuralComparison (Web)  (SDF)
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    5'-Methoxylariciresinol

    5'-Methoxylariciresinol
    Product Name 5'-Methoxylariciresinol
    CAS No.: 105256-12-0
    Catalog No.: CFN96706
    Molecular Formula: C21H26O7
    Molecular Weight: 390.43 g/mol
    Purity: >=98%
    Type of Compound: Lignans
    Physical Desc.: Powder
    Source: The callus cultures of Stellera chamaejasme.
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
    Price:
    Download: COA    MSDS
    Similar structural: Comparison (Web)  (SDF)
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    product package
  • Cell Death Dis.2019, 10(12):882
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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
    Biological Activity
    Description: 5'-Methoxylariciresinol is a natural product from Stellera chamaejasme.
    5'-Methoxylariciresinol Description
    Source: The callus cultures of Stellera chamaejasme.
    Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, 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 2.5613 mL 12.8064 mL 25.6128 mL 51.2256 mL 64.032 mL
    5 mM 0.5123 mL 2.5613 mL 5.1226 mL 10.2451 mL 12.8064 mL
    10 mM 0.2561 mL 1.2806 mL 2.5613 mL 5.1226 mL 6.4032 mL
    50 mM 0.0512 mL 0.2561 mL 0.5123 mL 1.0245 mL 1.2806 mL
    100 mM 0.0256 mL 0.1281 mL 0.2561 mL 0.5123 mL 0.6403 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. 2011 Dec;36(24):3457-62.
    Studies on chemical constitutes from callus cultures of Stellera chamaejasme.[Pubmed: 22368856]

    METHODS AND RESULTS:
    From callus cultures of Stellera chamaejasme, 17 compounds were isolated. Based on their physical and chemical data and spectroscopic analysis, they were identified as syringaresinol (1), medioresinol (2), pinoresinol (3), (1R, 2S, 5R, 6S)- 2-(4- hydroxyphenyl)-6-(3-methoxy-4-hydroxyphenyl)-3, 7-dioxabicyclo [3, 3, 0] octane (4), epipinoresinol (5), caruilignan D (6), 3-oxo-guai-4-ene-11, 12-diol (7), (-) -lariciresinol (8), tetrahydro-2-(4-hydroxy-3-methoxyphenyl)-4-[(4-hydroxyphenyl) methyl]-3-furanmethanol (9), 5'-Methoxylariciresinol (10), vladinol D (11), cyclo (L-Pro-L-Val) (12), oxomatairesinol (13), (+) -guayarol (14); acutissimalignan B (15), isolariciresinol (16), and beta-sitosterol (17), respectively.
    CONCLUSIONS:
    Among these compounds, 12 was a cyclodipeptide, 7 was a sesquiterpene, and the others except 17 were lignans. All compounds were first isolated from callus cultures of S. chamaejasme.
    Zhongguo Zhong Yao Za Zhi. 2012 May;37(9):1241-4.
    Non-alkaloid chemical constituents from Coptis chinensis.[Pubmed: 22803368]
    To separate and identify chemical constituents from Coptis chinensis.
    METHODS AND RESULTS:
    The compounds were separated and purified by various chromatographic techniques. Their structures were identified on the basis of their physicochemical properties using spectral techniques such as NMR and MS. Thirteen compounds were separated from ethanol extracts of C. chinensis, including seven lignans, three simple phenylpropanoids, two flavones and one phenolic acid, and identified as erythro-guaiacylglycerol-8-O-4'-(coniferyl alcohol) ether (1), threo-guaiacylglycerol-8-O-4'-(coniferyl alcohol) ether (2), (+)-pinoresinol (3), (+)-medioresinol (4), (+)-lariciresinol (5), (+)-5'-Methoxylariciresinol (6), (+)-isolariciresinol (7), chlorogenic acid (8), ferulic acid (9), Z-octadecyl caffeate (10), rhamnetin (11), wogonin (12), and vanillic acid (13).
    CONCLUSIONS:
    Compounds 1, 2, 4, 6, 10-13 were separated from the genus Coptis for the first time.
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