Wilforol A

Wilforol A
Product Name Wilforol A
CAS No.: 167882-66-8
Catalog No.: CFN92083
Molecular Formula: C29H38O5
Molecular Weight: 466.6 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The herbs of Tripterygium wilfordii Hook. f.
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Wilforol A is a natural product from Tripterygium wilfordii Hook. f.
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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.
  • Chemistry of Natural Compounds2019, 55(1):127-130
  • Biochem Pharmacol.2020, 178:114083
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  • J Control Release.2024, 375:300-315.
  • Sci Rep.2023, 13(1):21690.
  • Antioxidants (Basel).2021, 10(10):1620.
  • The Journal of Animal & Plant Sciences.2020, 30(6):1366-1373
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    Total Synthesis of Celastrol, Development of a Platform to Access Celastroid Natural Products.[Pubmed: 26331410 ]
    Celastroid natural products, triterpenes, have been and continue to be investigated in clinical trials.
    METHODS AND RESULTS:
    Celastrol, and for that matter any member of the celastroid family, was prepared for the first time through chemical synthesis starting from 2,3-dimethylbutadiene. A triene cyclization precursor generated in 12 steps underwent a nonbiomimetic polyene cyclization mediated by ferric chloride to generate the generic celastroid pentacyclic core.
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