Wilforol A
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.
Separation Science Plus2022, sscp.202200048.
Food Chem.2020, 327:126992.
bioRxiv - Molecular Biology2023, 535548.
Arch Toxicol.2017, 91(10):3225-3245
Front Pharmacol.2023, 14:1095083.
J Sci Food Agric.2017, 97(5):1656-1662
Phytomedicine.2018, 40:37-47
Food Sci Nutr.2019, 8(1):246-256
Current Enzyme Inhibition2023, 19(1):55-64(10)
J Health Sci Med Res.2023, 31584.
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J Am Chem Soc. 2015 Sep 23;137(37):11864-7.
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.
CONCLUSIONS:
In the cyclization, engagement of a tetrasubstituted olefin formed adjacent all carbon quaternary centers stereospecifically. With access to the carbocyclic core of the family of natural products, wilforic acid and Wilforol A were prepared en route to racemic celastrol.
