Calanolide E

Calanolide E
Product Name Calanolide E
CAS No.: 142566-61-8
Catalog No.: CFN99466
Molecular Formula: C22H28O6
Molecular Weight: 388.5 g/mol
Purity: >=98%
Type of Compound: Coumarins
Physical Desc.: Powder
Targets: HIV
Source: The barks of Calophyllum lanigerum
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Calanolide E2 has anti-HIV activity.
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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

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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    J Nat Prod. 1996 Aug;59(8):754-8.
    New pyranocoumarins isolated from Calophyllum lanigerum and Calophyllum teysmannii.[Pubmed: 8792623 ]

    METHODS AND RESULTS:
    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).
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    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.
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