Sanguisorbigenin

Sanguisorbigenin
Product Name Sanguisorbigenin
CAS No.: 6812-98-2
Catalog No.: CFN91139
Molecular Formula: C30H46O3
Molecular Weight: 454.7 g/mol
Purity: >=98%
Type of Compound: Triterpenoids
Physical Desc.: Powder
Source: The roots of Ilex asprella
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price: $413/5mg
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.
  • Ulm University Medical Center2020, doi: 10.18725.
  • Pharmaceutics.2020, 12(9):882.
  • J Appl Biol Chem2022, 65:343−348.
  • Metabolites. 2023, 13(11):1122.
  • Srinakharinwirot University2023, 2669.
  • Tea Res. Ins. Of China2017, 1-12
  • Journal of Ginseng Research2022, j.jgr.2022.09.005.
  • Biochem Pharmacol. 2023, 210:115463.
  • Int. J. Mol. Sci.2022, 23(8), 4130.
  • Free Radic Biol Med.2016, 97:307-319
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    Chinese Herbal Medicines, 2013, 5(1):1-4.
    Chemical Constituents in Charred Sanguisorbae Radix.[Reference: WebLink]
    To study the chemical constituents in the effective fractions of charred Sanguisorbae Radix.
    METHODS AND RESULTS:
    The compounds were isolated and purified by column chromatography and their structures were identified on the basis of physicochemical properties and spectral analysis. Five compounds were isolated and identified as 3β-hydroxy-28-norurs-17,19,21-trien (1), 3β-hydroxy-28-norurs-12,17-dien (2), 3β,19α-dihydroxyurs-13(18)-en-28-oic acid (3), 3β-[(α-L-arabin-opyranosyl) oxy]-28-norurs-12,17-dien (4), and pomolic acid (5).
    CONCLUSIONS:
    Compounds 1, 3, and 4 are novel compounds belong to triterpenoids and triterpenoid saponins, named as Sanguisorbigenins Z, Y1, and Y2, respectively.
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