Wedelialactone A

Wedelialactone A
Product Name Wedelialactone A
CAS No.: 175862-40-5
Catalog No.: CFN96439
Molecular Formula: C24H34O8
Molecular Weight: 450.53 g/mol
Purity: >=98%
Type of Compound: Sesquiterpenoids
Physical Desc.: Powder
Source: The herbs of Wedelia trilobata
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Reference standards.
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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.
  • J Clin Med.2022, 11(13):3662.
  • Journal of Apicultural Research2021, 60(1)
  • Plant Science2024, 338:111914
  • Molecules.2019, 24(22):E4022
  • Chemistr of plant2016, 2016021195
  • Hum Exp Toxicol.2017, 36(11):1169-1176
  • Korean Herb. Med. Inf.2021, 9(2):231-239.
  • J Appl Pharm Sci.2022, 12(04):044-053
  • Pharmacognosy Journal2019, 11(2): 369-373
  • Acta horticulturae2017, 1158:257-268
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    Process for preparing wedelia lactone and application thereof.[Reference: WebLink]

    METHODS AND RESULTS:
    The invention discloses a process for preparing Wedelialactone And application thereof, wherein 3,4-dihydroxy benzene and 2,4,6-trihydroxy benzaldehyde is used as the raw material, an intermediate A represented by formula (II) and an intermediate B represented by formula (III) are synthesized, which are subject to Sonogashira coupling reaction with carbonyl ring forming reaction to obtain wedelialactone.
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