Lethedioside A

Lethedioside A
Product Name Lethedioside A
CAS No.: 221289-31-2
Catalog No.: CFN98201
Molecular Formula: C29H34O15
Molecular Weight: 622.6 g/mol
Purity: >=98%
Type of Compound: Flavonoids
Physical Desc.: Powder
Source: The roots of Aquilaria sinensis (Lour.) Spreng.
Solvent: DMSO, Pyridine, Methanol, Ethanol, etc.
Price:
Lethedoside A was either inactive or weakly active against KB tumor cells, in contrast to previously isolated flavones from the same plant.
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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.
  • Molecules.2022, 27(7):2360.
  • Chem Pharm Bull (Tokyo).2017, 65(9):826-832
  • Korean J. Food Sci. & Technol.2022, 54(2):241-246
  • Am J Chin Med.2023, 51(7):1675-1709.
  • J Biochem Mol Toxicol.2017, 31(9)
  • Metabolites2023, 13(1), 3.
  • Environ Toxicol.2024, 39(4):2417-2428.
  • Sci Rep.2023, 13(1):13610.
  • J Sci Food Agric.2022, 102(4):1628-1639
  • Pharmacol Rep.2022, 74(1):175-188.
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    METHODS AND RESULTS:
    Five new 7-methoxy-flavone 5-O-glycosides were isolated from a cytotoxic MeOH extract of Lethedon tannaensis, and the structures were elucidated by 2D NMR spectral analysis and by chemical methods. Lethedoside A (1), lethedoside B (2), and lethedoside C (3) were 5-O-glucosides of 7,3', 4'-tri-O-methylluteolin, 7,3',4',5'-tetra-O-methyltricetin, and 7,3', 4'-tri-O-methytricetin, respectively; lethediosides A (4) and B (5) and a known compound 6 were 5-O-xylosylglucosides of 7,3', 4'-tri-O-methylluteolin, 7,3',4',5'-tetra-O-methyltricetin, and 7, 4'-di-O-methylapigenin, respectively.
    CONCLUSIONS:
    These flavonoids were either inactive or weakly active against KB tumor cells, in contrast to previously isolated flavones from the same plant.
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