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    Marilactone
    Marilactone
    Information
    CAS No. 34818-17-2 Price
    Catalog No.CFN89069Purity>=98%
    Molecular Weight154.16Type of CompoundPhenols
    FormulaC8H10O3Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison
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    Our products had been exported to the following research institutions and universities, And still growing.
  • Warszawski Uniwersytet Medyczny (Poland)
  • Pennsylvania State University (USA)
  • Chinese University of Hong Kong (China)
  • S.N.D.T. Women's University (India)
  • Lund University (Sweden)
  • National Research Council of Can... (Canada)
  • Biotech R&D Institute (USA)
  • Mahatma Gandhi University (India)
  • University of Helsinki (Finland)
  • Uniwersytet JagielloĊ„ski w Krak... (Poland)
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    Marilactone Description
    Source: The metabolites of the fungus Stachylidium sp.
    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 6.4868 mL 32.4338 mL 64.8677 mL 129.7353 mL 162.1692 mL
    5 mM 1.2974 mL 6.4868 mL 12.9735 mL 25.9471 mL 32.4338 mL
    10 mM 0.6487 mL 3.2434 mL 6.4868 mL 12.9735 mL 16.2169 mL
    50 mM 0.1297 mL 0.6487 mL 1.2974 mL 2.5947 mL 3.2434 mL
    100 mM 0.0649 mL 0.3243 mL 0.6487 mL 1.2974 mL 1.6217 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.
    Marilactone References Information
    Citation [1]

    J Nat Prod. 2013 Mar 22;76(3):322-6.

    Unprecedented polyketides from a marine sponge-associated Stachylidium sp.[Pubmed: 23268694 ]
    From the marine sponge-derived fungus Stachylidium sp. six novel phthalide-related compounds, cyclomarinone (1), maristachones A-E (2-5), and Marilactone (6), were isolated. The structure of compound 1 comprises a hydroxycyclopentenone ring instead of the furanone ring characteristic for phthalides and represents a new carbon arrangement within polyketides. In the epimeric compounds 5a and 5b the phthalide (=isobenzofuranone) nucleus is modified to an isobenzofuran ring with ketal and acetal functionalities. Biosynthetically the structural skeletons of cyclomarinone (1) and maristachones A (2), C (4), D (5a), and E (5b) are most unusual due to the presence of an additional carbon atom when compared to the basic polyketide skeleton. This special biosynthetic feature also holds true for the likewise isolated polyketide Marilactone (6).