Parvifolixanthone B

Parvifolixanthone B
Product Name Parvifolixanthone B
CAS No.: 906794-57-8
Catalog No.: CFN89129
Molecular Formula: C24H26O6
Molecular Weight: 410.46 g/mol
Purity: >=98%
Type of Compound: Xanthones
Physical Desc.: Powder
Source: The twigs of Garcinia parvifolia.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Parvifolixanthone B is a natural product from Garcinia parvifolia.
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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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    Tetrahedron, 2006, 62(36):8578-8585.
    Phloroglucinols, depsidones and xanthones from the twigs of Garcinia parvifolia.[Reference: WebLink]

    METHODS AND RESULTS:
    Seven phloroglucinols, named parvifoliols A–G (1–7), two depsidones, named parvifolidones A, B (8, 9), and three xanthones, named parvifolixanthone A, Parvifolixanthone B, parvifolixanthone C (10–12), were isolated from the twigs of Garcinia parvifolia along with seven known compounds: garcidepsidone B, mangostinone, rubraxanthone, dulxanthone D, 1,3,5,6-tetrahydroxyxanthone, norathyriol, and (2E,6E,10E)-(+)-4β-hydroxy-3-methyl-5β-(3,7,11,15-tetramethylhexadeca-2,6,10,14-tetraenyl)cyclohex-2-en-1-one.
    CONCLUSIONS:
    Their structures were proposed on the basis of spectroscopic data. The antibacterial and antioxidation activities were evaluated.
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