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    Glycozolinine
    Glycozolinine
    Information
    CAS No. 5257-08-9 Price
    Catalog No.CFN98862Purity>=98%
    Molecular Weight197.2 Type of CompoundAlkaloids
    FormulaC13H11NOPhysical DescriptionPowder
    Download     COA    MSDS    SDFSimilar structuralComparison (Web)
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    Glycozolinine Description
    Source: The herbs of Micromelum sp.
    Biological Activity or Inhibitors:
    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

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    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 5.071 mL 25.355 mL 50.7099 mL 101.4199 mL 126.7748 mL
    5 mM 1.0142 mL 5.071 mL 10.142 mL 20.284 mL 25.355 mL
    10 mM 0.5071 mL 2.5355 mL 5.071 mL 10.142 mL 12.6775 mL
    50 mM 0.1014 mL 0.5071 mL 1.0142 mL 2.0284 mL 2.5355 mL
    100 mM 0.0507 mL 0.2535 mL 0.5071 mL 1.0142 mL 1.2677 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.
    Glycozolinine References Information
    Citation [1]

    Phytochemistry Volume 22, Issue 4, 1983, Pages 1064-1065

    Glycozolinine, a carbazole derivative from Glycosmis pentaphilla[Reference: WebLink]
    A new carbazole derivative, Glycozolinine, was isolated from the seeds of Glycosmis pentaphylla. From physical and chemical evidence its structure is 6-hydroxy-3-methylcarbazole.
    Citation [2]

    Tetrahedron Volume 71, Issue 21, 27 May 2015, Pages 3485–3490

    Total synthesis of glycomaurrol and eustifoline-C by DIBAL-H promoted reductive ring opening of pyrano[2,3-c]carbazoles[Reference: WebLink]
    The palladium-catalyzed construction of the carbazole framework provides an efficient access to 3-hydroxy-6-methylcarbazole (Glycozolinine) (5). Regioselective annulation of a pyran ring at Glycozolinine (5) using either a C5- or a C10-building block leads to the pyrano[2,3-c]carbazole alkaloids glycomaurin (5,6-pyranoglycozoline, eustifoline-A) (2) and eustifoline-B (4), respectively.