Pungiolide A

Pungiolide A
Product Name Pungiolide A
CAS No.: 130395-54-9
Catalog No.: CFN80472
Molecular Formula: C30H36O7
Molecular Weight: 508.6 g/mol
Purity: >=98%
Type of Compound: Sesquiterpenoids
Physical Desc.: Powder
Source: The herbs of Xanthium pungens
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Pungiolide A exhibits moderate cytotoxicities with IC50 values in the range of 0.90-6.84 uM.
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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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  • Universiti Tunku Aboul Rahman2023, 6263.
  • Hortic Res.2023, 10(4):uhad039.
  • Appl Microbiol Biotechnol.2018, 102(12):5105-5120
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    Phytochemistry. 2016 Dec;132:115-122.
    Cytotoxic dimeric xanthanolides from fruits of Xanthium chinense.[Pubmed: 27772796 ]
    Nine dimeric xanthanolides, pungiolides F-N, and five known analogues, pungiolides A-E, were isolated from fruits of Xanthium chinense.
    METHODS AND RESULTS:
    Their structures were elucidated through spectroscopic and electronic circular dichroism (ECD) analyses. Pungiolide F is a xanthanolide dimer with an acyclic linkage. Five of the dimers, pungiolide H, pungiolide L, Pungiolide A, pungiolide C and pungiolide E, exhibited moderate cytotoxicities with IC50 values in the range of 0.90-6.84 μM using taxol as the positive control, which had, by comparison, IC50 values in the range of 0.00118-0.0675 μM.
    CONCLUSIONS:
    These findings enrich the structural diversity of dimeric sesquiterpene lactones.
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