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    Calanolide E
    Calanolide E
    Information
    CAS No. 142566-61-8 Price
    Catalog No.CFN99466Purity>=98%
    Molecular Weight388.5 Type of CompoundCoumarins
    FormulaC22H28O6Physical DescriptionPowder
    Download Manual    COA    MSDSSimilar structuralComparison (Web)
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    Our products had been exported to the following research institutions and universities, And still growing.
  • FORTH-IMBB (Greece)
  • MTT Agrifood Research Finland (Finland)
  • Donald Danforth Plant Science Ce... (USA)
  • Max Rubner-Institut (MRI) (Germany)
  • University of Liège (Belgium)
  • Kitasato University (Japan)
  • University of Zurich (Switzerland)
  • VIB Department of Plant Systems ... (Belgium)
  • Indian Institute of Science (India)
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  • Srinakharinwirot University (Thailand)
  • More...
  • Package
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    Biological Activity
    Description: 1. Calanolide E2 has anti-HIV activity.
    Targets: HIV
    Calanolide E Description
    Source: The barks of Calophyllum lanigerum
    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 2.574 mL 12.87 mL 25.74 mL 51.4801 mL 64.3501 mL
    5 mM 0.5148 mL 2.574 mL 5.148 mL 10.296 mL 12.87 mL
    10 mM 0.2574 mL 1.287 mL 2.574 mL 5.148 mL 6.435 mL
    50 mM 0.0515 mL 0.2574 mL 0.5148 mL 1.0296 mL 1.287 mL
    100 mM 0.0257 mL 0.1287 mL 0.2574 mL 0.5148 mL 0.6435 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.
    Calanolide E References Information
    Citation [1]

    J Nat Prod. 1996 Aug;59(8):754-8.

    New pyranocoumarins isolated from Calophyllum lanigerum and Calophyllum teysmannii.[Pubmed: 8792623 ]
    During a chemotaxonomic survey of Calophyllum extracts present in the National Cancer Institute's natural product repository, four new pyranocoumarins were isolated from extracts of C. lanigerum var. austrocoriaceum and C. teysmannii var. inophylloide (King.) P. F. Stevens (Clusiaceae). The structure elucidation and anti-HIV activity of Calanolide E2 (4), cordatolide E (5), pseudocordatolide C (6), and calanolide F (9), along with a simple prenylated coumarin precursor (11), are described here.