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    Methylophiopogonone B
    Information
    CAS No. 74805-89-3 Price
    Catalog No.CFN80321Purity>=98%
    Molecular Weight326.34Type of CompoundFlavonoids
    FormulaC19H18O5Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)
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    Methylophiopogonone B Description
    Source: The roots of Ophiopogon japonicus
    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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    Recently, ChemFaces products have been cited in many studies from excellent and top scientific journals

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.

    PMID: 29328914

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.

    PMID: 29149595

    Scientific Reports 2017 Dec 11;7(1):17332.
    doi: 10.1038/s41598-017-17427-6.

    PMID: 29230013

    Molecules. 2017 Oct 27;22(11). pii: E1829.
    doi: 10.3390/molecules22111829.

    PMID: 29077044

    J Cell Biochem. 2018 Feb;119(2):2231-2239.
    doi: 10.1002/jcb.26385.

    PMID: 28857247

    Phytomedicine. 2018 Feb 1;40:37-47.
    doi: 10.1016/j.phymed.2017.12.030.

    PMID: 29496173
    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 3.0643 mL 15.3214 mL 30.6429 mL 61.2858 mL 76.6072 mL
    5 mM 0.6129 mL 3.0643 mL 6.1286 mL 12.2572 mL 15.3214 mL
    10 mM 0.3064 mL 1.5321 mL 3.0643 mL 6.1286 mL 7.6607 mL
    50 mM 0.0613 mL 0.3064 mL 0.6129 mL 1.2257 mL 1.5321 mL
    100 mM 0.0306 mL 0.1532 mL 0.3064 mL 0.6129 mL 0.7661 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.
    Methylophiopogonone B References Information
    Citation [1]

    Zhongguo yao xue za zhi,2005,40(5):337-341.

    Studies on the liposoluble components from tuber of Ophiopogon japonicus.[Reference: WebLink]
    The compounds were isolated by column chromatography with silica gel and Sephadex LH-20 and the structures were elucidated by spectras' analysis. Sixteen compounds were obtained as 7 homoisoflavones, 2 anthraquinones, 3 phenolic acids, 2 terpenes and 2 fatty acids. Their structures were identified as methylophiopogonanone A(I), methylophiopogonanone B(II), methylophiopogonone A(III), Methylophiopogonone B(IV), 2'-hydroxy-methylophiopogonone A(V), 6-aldehycto-isoophiopogo-nanone A(VI), 5,7-dihyelroxy-8-methoxy-6-methyl-3-(2'-hydroxy-4'-methoxybenzyl) chroman-4-one(VII), chrysophenol(VIII), emodin(IX), vanillic acid(X), P-hydroxy benzaldenhyde (XI), P-trans-coumarinic acid(XII), l-borneol-#beta#-D-glucopyranoside (XIII), oleanolia acid(XIV), azelaic acid (XV) and n-tricosanoic acid(XVI). The compound IV, VIII--XII and XIV--XVI were isolated from O. japonicus and the genus Ophiopogon for the first time, respectively. The types of anthraquinone, phenolic acid and triterpene were firstly obtained from the genus.