Acuminatanol

Acuminatanol
Product Name Acuminatanol
CAS No.: 948884-38-6
Catalog No.: CFN96555
Molecular Formula: C30H22O16
Molecular Weight: 638.49 g/mol
Purity: >=98%
Type of Compound: Flavonoids
Physical Desc.: Powder
Source: The herbs of Trichoscypha acuminata.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Acuminatanol is a natural product from Trichoscypha acuminata.
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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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  • Purinergic Signal.2024, doi: 10.1007.
  • The Thai Journal of Pharmaceutical Sciences2023, 47(3):3.
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    Acuminatanol, the First 2′,2′′-Bis-dihydrobiflavonol from the Aqueous Extract of Trichoscypha acuminata.[Reference: WebLink]

    METHODS AND RESULTS:
    One new 3′,4′,5′,5,7-pentahydroxy-2′,2‴-bis-dihydrobiflavonol, Acuminatanol (1), was obtained from the aqueous extract of Trichoscypha acuminata. The structure elucidation process was performed primarily utilizing a capillary scale NMR probe. Acuminatanol (1) is the first example of a bis-dihydroflavonol linked exclusively via the B-rings at C-2′ and C-2‴ positions.
    CONCLUSIONS:
    To date, it is the first naturally-occurring compound reported from the genus Trichoscypha, and the first new natural product published from our compound libraries generated from the aqueous extracts of American and African plants.
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