Aurantiamide benzoate

Aurantiamide benzoate
Product Name Aurantiamide benzoate
CAS No.: 150881-02-0
Catalog No.: CFN91929
Molecular Formula: C32H30N2O4
Molecular Weight: 506.59 g/mol
Purity: >=98%
Type of Compound: Alkaloids
Physical Desc.: Powder
Source: The herbs of Inula cappa
Solvent: Chloroform, Dichloromethane, Ethyl Acetate, DMSO, Acetone, etc.
Price:
Aurantiamide benzoate exhibits moderate inhibitory activity against xanthine oxidase.
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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.
  • Biosci Biotechnol Biochem.2020, 84(3):621-632
  • Pharmacognosy Journal.2022, 14,4,327-337.
  • Front Pharmacol.2022, 13:806869.
  • J Food Sci Technol.2019, 56(5):2712-2720
  • Pharmacia2024, 71:1-9.
  • Pharmacognosy Magazine2017, 13(52):868-874
  • Food and Chemical Toxicology2020, 111221
  • Neuropharmacology2019, 151437
  • Front Cell Infect Microbiol.2018, 8:292
  • Preprints2022, 2022030063.
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    METHODS AND RESULTS:
    Four known compounds obtained from these herbs were identified as 3alpha, 24-dihydoxylurs-12-en-28-oic acid, betulinic acid, aurantiamide acetate, and Aurantiamide benzoate by spectroscopic means. 3alpha, 24-Dihydoxylurs-12-en-28-oic acid has potent inhibitory activity against Streptococcus salivarius, Streptococcus pneumoniae, Streptococcus pyogenes, and Porphyromomas gingivalis. Aurantiamide benzoate exhibited moderate inhibitory activity against xanthine oxidase.
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    METHODS AND RESULTS:
    The constituents were isolated and purified by column chromatography and the structures were identified by physicochemical properties and spectral analysis. Six compounds were obtained as Aurantiamide benzoate (1), aurantiamide acetate (2), 1-O-octacosanoylgerol (3), beta-sitosterol (4), daucesterol (5), ferulic acid (6).
    CONCLUSIONS:
    All these compounds were obtained from this plant for the first time. Compounds 1 and 2 were isolated for the first time from this genus.
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