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    Daphnicyclidin F
    Daphnicyclidin F
    Information
    CAS No. 385384-26-9 Price
    Catalog No.CFN96778Purity>=98%
    Molecular Weight397.47Type of CompoundAlkaloids
    FormulaC23H27NO5Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)
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    Daphnicyclidin F Description
    Source: The stems of Daphniphyllum humile and D.teijsmanni.
    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

    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 2.5159 mL 12.5796 mL 25.1591 mL 50.3183 mL 62.8978 mL
    5 mM 0.5032 mL 2.5159 mL 5.0318 mL 10.0637 mL 12.5796 mL
    10 mM 0.2516 mL 1.258 mL 2.5159 mL 5.0318 mL 6.2898 mL
    50 mM 0.0503 mL 0.2516 mL 0.5032 mL 1.0064 mL 1.258 mL
    100 mM 0.0252 mL 0.1258 mL 0.2516 mL 0.5032 mL 0.629 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.
    Daphnicyclidin F References Information
    Citation [1]

    J Am Chem Soc. 2001 Nov 21;123(46):11402-8.

    Daphnicyclidins A-H, novel hexa- or pentacyclic alkaloids from two species of Daphniphyllum.[Pubmed: 11707117]
    Eight highly modified Daphniphyllum alkaloids with unprecedented fused hexa- or pentacyclic skeletons, daphnicyclidin A,daphnicyclidin B, daphnicyclidin C, daphnicyclidin D, daphnicyclidin E, Daphnicyclidin F, daphnicyclidin G, daphnicyclidin H (1-8), have been isolated from the stems of Daphniphyllum humile and D.teijsmanni, and their structures were elucidated on the basis of spectroscopic data and chemical means. The stereochemistry was elucidated by combination of NOESY correlations, X-ray crystallographic data, and CD analyses.