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    CAS No. 117456-87-8 Price
    Catalog No.CFN96476Purity>=98%
    Molecular Weight346.46Type of CompoundDiterpenoids
    FormulaC21H30O4Physical DescriptionPowder
    Download     COA    MSDSSimilar structuralComparison (Web)
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    Our products had been exported to the following research institutions and universities, And still growing.
  • Periyar University (India)
  • Nicolaus Copernicus Uniwersity (Poland)
  • Sri Ramachandra University (India)
  • Universidade Católica Portuguesa (Portugal)
  • Warszawski Uniwersytet Medyczny (Poland)
  • John Innes Centre (United Kingdom)
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  • More...
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    Triptonodiol Description
    Source: The roots of Tripterygium wilfordii Hook.f.
    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.

    PMID: 29496173
    Calculate Dilution Ratios(Only for Reference)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.8863 mL 14.4317 mL 28.8634 mL 57.7267 mL 72.1584 mL
    5 mM 0.5773 mL 2.8863 mL 5.7727 mL 11.5453 mL 14.4317 mL
    10 mM 0.2886 mL 1.4432 mL 2.8863 mL 5.7727 mL 7.2158 mL
    50 mM 0.0577 mL 0.2886 mL 0.5773 mL 1.1545 mL 1.4432 mL
    100 mM 0.0289 mL 0.1443 mL 0.2886 mL 0.5773 mL 0.7216 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.
    Triptonodiol References Information
    Citation [1]

    Helvetica Chimica Acta, 2013 , 96 (2) :313-9.

    Two New Abietane Diterpenoids from the Roots of Tripterygium wilfordii HOOK. f.[Reference: WebLink]
    Two new abietane-type diterpenoids, named triptobenzene R (1) and triptobenzene S (2), together with three known abietane-type diterpenoids, triptophenolide (3), Triptonodiol (4), and triptonoterpene methyl ether (5), were isolated from the roots of Tripterygium wilfordii Hook. f. Their structures and relative configurations were established by detailed spectral studies, including 1D- and 2D-NMR (HSQC, HMBC, and NOESY), and HR-ESI-TOF-MS, and by comparison with published data. Their absolute configurations were assigned by the CD technique, applied for the first time to abietane diterpenes from Tripterygium wilfordii. Compound 2 is the first abietane-type norditerpenoid isolated from the genus Tripterygium.
    Citation [2]

    Planta Med. 1988 Aug;54(4):330-2.

    Studies on New Components and Stereochemistry of Diterpenoids from Trypterygium wilfordii.[Pubmed: 17265278 ]
    An extensive investigation of the petroleum ether extract of TRIPTERYGIUM WILFORDII plants have revealed the presence of four new compounds, triptonoterpene, neotriptonoterpene, Triptonodiol, and neotriptonolide, in addition to the diterpenes isolated and characterized earlier. The structures of these novel natural products have been elucidated.